58 Researchers jobs in Oxford
Senior Research Associate
Oxford, South East
AbbVie
Posted 21 days ago
Job Viewed
Job Description
Company Description
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
+ Based at DJS Antibodies in Headington, Oxford
+ Reporting to Senior Scientist II
At DJS Antibodies, we aspire to create the next generation of antibody therapeutics and in doing so improving the prognosis for patients with life-changing immunological diseases and cancers. As a biotech company within AbbVie, we combine the agility, team spirit and scientific focus of a biotech with the reach and vision of a global pharmaceutical company. We have developed a number of drug candidates to date and are looking forward to growing our portfolio to have the biggest impact on patients' lives.
A critical part of achieving our vision is working with fantastic people, and as such we are looking for an enthusiastic and talented Research Assistant/Senior Research Assistant to join the team. For this role, candidates should be excited about working in a small, dynamic team; always keen to get involved with all aspects of research at DJS; be a team player; have a high level of skill and passion for in vivo work. This position represents an excellent opportunity for someone looking to begin or solidify their career within an industry laboratory research environment working on innovative projects whilst developing a variety of new skills.
Job Overview
The successful candidate will work closely with the PPL holder to plan experiments such as immunisation to generate antibody responses and testing the biological effects of lead antibodies that we have discovered. They will be responsible for preparing biological materials for these experiments, performing the required in vivo techniques and analysing the results. They will also have the opportunity to carry out laboratory experiments utilising molecular biology, cell culture, antibody production and various assay techniques to support the DJS discovery activities as a key member of the team. In addition to on-site laboratory work they will be required to work with live rodent models and animal derived tissues in the off-site facility for up to 50% of time.
At DJS, we want to foster innovative scientists performing cutting-edge science. A successful applicant will be a practical person who is organised, pays attention to detail, and efficiently gets the job done. Previous experience in a range of analytical techniques is preferred but is not essential as training will be provided.
They will have many opportunities for scientific career development and improvement of their knowledge of a world leading R&D/drug development pipeline and the broader business both at DJS and within AbbVie.
Successful applicant's key responsibilities
+ Bringing energy, enthusiasm and positivity to the company
+ Animal model husbandry
+ Performing experiments with live animals
+ Collection of animal derived tissues
+ Maintenance of cell cultures
+ Transient protein expression with mammalian cell lines
+ Work as a key member of the DJS discovery team
+ Performing critical laboratory experiments and analysing the data to contribute to strategic decision making within DJS discovery
+ Keeping up to date with developments in the literature in relation to technical aspects of drug discovery technologies
+ Day-to-day laboratory management as part of the team e.g. maintaining a safe and clean working laboratory environment, re-ordering laboratory consumables
+ Establishing and maintaining quality sample archives
+ Gathering, analysing and presenting data from a variety of sources to the wider team and organization
+ Critical and impartial review of self and peer generated laboratory data
+ Maintenance of laboratory experimental records
+ Follow established procedures, protocols and study plans and recommend changes for refinement. Adhere to regulatory requirements.
Qualifications
+ A BSc of 2:1 level or higher with intercalated year in industrial/academic research and/or an MSc/MRes or higher degree with significant lab experience in a relevant discipline (such as Biology, Biochemistry, pathology, cell biology or Natural Sciences)
+ A current UK PIL AB licence (or equivalent) with 5 years experience in working with animal models.
+ Proven competencies in in vivo procedures in experimental rodents
+ For example: intravenous, intramuscular, intrapertitoneal, sub-cutaneous injections, blood sampling, schedule 1 methods, use of anesthetics.
+ It will be a requirement to pass a 6-month probationary period at DJS that the candidate is declared competent in all relevant techniques by the vivarium staff.
+ Enthusiasm for and commitment to drug discovery and drug development research
+ Proven recent experience in
+ Performing in vivo experiments in experimental rodents
+ Mammalian cell culture
+ Molecular and biochemical techniques (such as; bacterial cell culture; flow cytometry; PCR; ELISA; protein expression and purification)
+ Evidence of excellent organizational and interpersonal skills including
+ Ability to work both independently and as part of a team
+ Ability to work efficiently with strong attention to detail
+ Ability to build effective working relationships
+ Laboratory method development
+ Ability to work flexible hours when required
+ Proven written and oral communicative ability
+ Problem-solving skills
+ Strong IT skills
+ Desirable skills
+ + Experience with running experimental models of inflammation in rodents
+ PIL C licence and experience with surgical techniques. Good knowledge of statistics
Additional Information
About DJS Antibodies
At DJS Antibodies as part of AbbVie our ambition is to contribute world class novel antibody therapeutics for the treatment of severe diseases into AbbVies clinical pipeline. Our proprietary antibody discovery technology enables us to discover first in class antibodies to the key drivers of disease that have, until now, been intractable to drug discovery such as GPCR's and other complex membrane and soluble targets.
Working at DJS will involve coming into a stimulating and entrepreneurial work environment with excellent exposure to industry-leading experts. Being part of a small team means that you will be exposed to all aspects of R&D and the broader business. You will benefit from working with a great team, a competitive remuneration package and significant opportunities for career development.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok ( .
Job Description
+ Based at DJS Antibodies in Headington, Oxford
+ Reporting to Senior Scientist II
At DJS Antibodies, we aspire to create the next generation of antibody therapeutics and in doing so improving the prognosis for patients with life-changing immunological diseases and cancers. As a biotech company within AbbVie, we combine the agility, team spirit and scientific focus of a biotech with the reach and vision of a global pharmaceutical company. We have developed a number of drug candidates to date and are looking forward to growing our portfolio to have the biggest impact on patients' lives.
A critical part of achieving our vision is working with fantastic people, and as such we are looking for an enthusiastic and talented Research Assistant/Senior Research Assistant to join the team. For this role, candidates should be excited about working in a small, dynamic team; always keen to get involved with all aspects of research at DJS; be a team player; have a high level of skill and passion for in vivo work. This position represents an excellent opportunity for someone looking to begin or solidify their career within an industry laboratory research environment working on innovative projects whilst developing a variety of new skills.
Job Overview
The successful candidate will work closely with the PPL holder to plan experiments such as immunisation to generate antibody responses and testing the biological effects of lead antibodies that we have discovered. They will be responsible for preparing biological materials for these experiments, performing the required in vivo techniques and analysing the results. They will also have the opportunity to carry out laboratory experiments utilising molecular biology, cell culture, antibody production and various assay techniques to support the DJS discovery activities as a key member of the team. In addition to on-site laboratory work they will be required to work with live rodent models and animal derived tissues in the off-site facility for up to 50% of time.
At DJS, we want to foster innovative scientists performing cutting-edge science. A successful applicant will be a practical person who is organised, pays attention to detail, and efficiently gets the job done. Previous experience in a range of analytical techniques is preferred but is not essential as training will be provided.
They will have many opportunities for scientific career development and improvement of their knowledge of a world leading R&D/drug development pipeline and the broader business both at DJS and within AbbVie.
Successful applicant's key responsibilities
+ Bringing energy, enthusiasm and positivity to the company
+ Animal model husbandry
+ Performing experiments with live animals
+ Collection of animal derived tissues
+ Maintenance of cell cultures
+ Transient protein expression with mammalian cell lines
+ Work as a key member of the DJS discovery team
+ Performing critical laboratory experiments and analysing the data to contribute to strategic decision making within DJS discovery
+ Keeping up to date with developments in the literature in relation to technical aspects of drug discovery technologies
+ Day-to-day laboratory management as part of the team e.g. maintaining a safe and clean working laboratory environment, re-ordering laboratory consumables
+ Establishing and maintaining quality sample archives
+ Gathering, analysing and presenting data from a variety of sources to the wider team and organization
+ Critical and impartial review of self and peer generated laboratory data
+ Maintenance of laboratory experimental records
+ Follow established procedures, protocols and study plans and recommend changes for refinement. Adhere to regulatory requirements.
Qualifications
+ A BSc of 2:1 level or higher with intercalated year in industrial/academic research and/or an MSc/MRes or higher degree with significant lab experience in a relevant discipline (such as Biology, Biochemistry, pathology, cell biology or Natural Sciences)
+ A current UK PIL AB licence (or equivalent) with 5 years experience in working with animal models.
+ Proven competencies in in vivo procedures in experimental rodents
+ For example: intravenous, intramuscular, intrapertitoneal, sub-cutaneous injections, blood sampling, schedule 1 methods, use of anesthetics.
+ It will be a requirement to pass a 6-month probationary period at DJS that the candidate is declared competent in all relevant techniques by the vivarium staff.
+ Enthusiasm for and commitment to drug discovery and drug development research
+ Proven recent experience in
+ Performing in vivo experiments in experimental rodents
+ Mammalian cell culture
+ Molecular and biochemical techniques (such as; bacterial cell culture; flow cytometry; PCR; ELISA; protein expression and purification)
+ Evidence of excellent organizational and interpersonal skills including
+ Ability to work both independently and as part of a team
+ Ability to work efficiently with strong attention to detail
+ Ability to build effective working relationships
+ Laboratory method development
+ Ability to work flexible hours when required
+ Proven written and oral communicative ability
+ Problem-solving skills
+ Strong IT skills
+ Desirable skills
+ + Experience with running experimental models of inflammation in rodents
+ PIL C licence and experience with surgical techniques. Good knowledge of statistics
Additional Information
About DJS Antibodies
At DJS Antibodies as part of AbbVie our ambition is to contribute world class novel antibody therapeutics for the treatment of severe diseases into AbbVies clinical pipeline. Our proprietary antibody discovery technology enables us to discover first in class antibodies to the key drivers of disease that have, until now, been intractable to drug discovery such as GPCR's and other complex membrane and soluble targets.
Working at DJS will involve coming into a stimulating and entrepreneurial work environment with excellent exposure to industry-leading experts. Being part of a small team means that you will be exposed to all aspects of R&D and the broader business. You will benefit from working with a great team, a competitive remuneration package and significant opportunities for career development.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
This advertiser has chosen not to accept applicants from your region.
0
Experienced Clinical Research Associate
Reading, South East
IQVIA
Posted 12 days ago
Job Viewed
Job Description
Our team is growing, join us on our mission to drive healthcare forward!
What We Offer / USPs
+ The chance to work on cutting edge medicines at the forefront of new medicines development
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
+ We offer genuine career development opportunities for those who want to grow as part of the organization
+ We invest in keeping our teams stable, so workload is consistent
+ As a CRA you will receive an iPad and use of key developments such as site visit app's, site visit report app's that allow CRA's to do their day job more efficiently
Responsibilities
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
+ If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis
+ If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement
Requirements
+ You should be life science degree educated
+ You have experience of independent on-site monitoring experience
+ You've handled multiple protocols and sites across a variety of drug indications
+ Flexibility and ability to travel
+ Strong communication, written and presentation skills
*** This role is not eligible for UK Visa Sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
What We Offer / USPs
+ The chance to work on cutting edge medicines at the forefront of new medicines development
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
+ We offer genuine career development opportunities for those who want to grow as part of the organization
+ We invest in keeping our teams stable, so workload is consistent
+ As a CRA you will receive an iPad and use of key developments such as site visit app's, site visit report app's that allow CRA's to do their day job more efficiently
Responsibilities
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
+ If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis
+ If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement
Requirements
+ You should be life science degree educated
+ You have experience of independent on-site monitoring experience
+ You've handled multiple protocols and sites across a variety of drug indications
+ Flexibility and ability to travel
+ Strong communication, written and presentation skills
*** This role is not eligible for UK Visa Sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
1
Experienced Clinical Research Associate
Reading, South East
IQVIA
Posted 12 days ago
Job Viewed
Job Description
Join Us on Our Mission to Drive Healthcare Forward
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
Why IQVIA?
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
Responsibilities
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
Requirements
+ Experience of independent on-site monitoring
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Life science degree educated or equivalent industry experience
+ Flexibility to travel to sites
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
#LI-ADAMTHOMPSON
*Please note - this role is not eligible for UK visa sponsorship*
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
IQVIA cFSP (sponsor-dedicated) are seeking experienced Clinical Research Associates in the UK.
Why IQVIA?
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
Responsibilities
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
Requirements
+ Experience of independent on-site monitoring
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Life science degree educated or equivalent industry experience
+ Flexibility to travel to sites
Apply today and forge a career with greater purpose, make an impact, and never stop learning!
#LI-ADAMTHOMPSON
*Please note - this role is not eligible for UK visa sponsorship*
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
2
Clinical Research Associate I
Reading, South East
IQVIA
Posted 18 days ago
Job Viewed
Job Description
**Join Us on Our Mission to Drive Healthcare Forward**
As a Clinical Research Associate at IQVIA, you'll play a vital role in advancing clinical research and improving patient outcomes. We're expanding our Site Management team and looking for passionate CRAs who are ready to make a difference. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials.
**Why IQVIA?**
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
**Responsibilities**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
**Profile**
+ Over 12 months of independent on-site monitoring experience, ensuring compliance with GCP, protocol requirements, and regulatory guidelines.
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ Hands-on experience in the Oncology therapeutic area.
+ Flexibility and commitment to nationwide travel
** This role is not eligible for UK Visa Sponsorship**
#LI-AdamThompson
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
As a Clinical Research Associate at IQVIA, you'll play a vital role in advancing clinical research and improving patient outcomes. We're expanding our Site Management team and looking for passionate CRAs who are ready to make a difference. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials.
**Why IQVIA?**
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
**Responsibilities**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
**Profile**
+ Over 12 months of independent on-site monitoring experience, ensuring compliance with GCP, protocol requirements, and regulatory guidelines.
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ Hands-on experience in the Oncology therapeutic area.
+ Flexibility and commitment to nationwide travel
** This role is not eligible for UK Visa Sponsorship**
#LI-AdamThompson
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Associate II
Reading, South East
IQVIA
Posted 18 days ago
Job Viewed
Job Description
**Join Us on Our Mission to Drive Healthcare Forward**
As a Clinical Research Associate at IQVIA, you'll play a vital role in advancing clinical research and improving patient outcomes. We're expanding our Site Management team and looking for passionate CRAs who are ready to make a difference. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials.
**Why IQVIA?**
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
**Responsibilities**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
**Profile**
+ Over 2 years of independent on-site monitoring experience, ensuring compliance with GCP, protocol requirements, and regulatory guidelines.
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ Hands-on experience in the Oncology therapeutic area.
+ Flexibility and commitment to nationwide travel
** This role is not eligible for UK Visa Sponsorship**
#LI-AdamThompson
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
As a Clinical Research Associate at IQVIA, you'll play a vital role in advancing clinical research and improving patient outcomes. We're expanding our Site Management team and looking for passionate CRAs who are ready to make a difference. This role offers a mix of on-site and remote monitoring, supporting work-life balance while contributing to cutting-edge clinical trials.
**Why IQVIA?**
+ IQVIA is recognized as #1 in its category on the 2025 Fortune® World's Most Admired Companies list for the FOURTH consecutive year!
+ We offer genuine career development opportunities for those who want to grow as part of the organization.
+ The chance to work on cutting edge medicines at the forefront of new medicines development.
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
**Responsibilities**
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
**Profile**
+ Over 2 years of independent on-site monitoring experience, ensuring compliance with GCP, protocol requirements, and regulatory guidelines.
+ You have successfully managed multiple clinical trial protocols across diverse investigative sites.
+ Hands-on experience in the Oncology therapeutic area.
+ Flexibility and commitment to nationwide travel
** This role is not eligible for UK Visa Sponsorship**
#LI-AdamThompson
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
4
Senior Clinical Research Associate (Oncology)
OX1 1AA Oxford, South East
£50000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a globally recognised pharmaceutical company at the forefront of cancer research, is seeking a highly motivated Senior Clinical Research Associate (CRA) to join their dedicated team. This hybrid role is based in the vibrant city of Oxford, Oxfordshire, UK , and plays a critical part in advancing groundbreaking oncology treatments. As a Senior CRA, you will be responsible for overseeing and managing clinical trial sites, ensuring adherence to protocol, regulatory requirements, and Good Clinical Practice (GCP) standards.
Responsibilities:
Qualifications:
This hybrid position offers a dynamic work environment, blending remote flexibility with essential on-site engagement, providing a significant opportunity to contribute to life-saving cancer therapies.
Responsibilities:
- Conduct site initiation, monitoring, and close-out visits for Phase I-IV oncology clinical trials.
- Ensure the accurate and timely collection, verification, and reporting of clinical data from study sites.
- Manage investigational product accountability and ensure compliance with study protocols.
- Build and maintain strong working relationships with Principal Investigators (PIs), site staff, and study sponsors.
- Identify, assess, and qualify potential clinical trial sites.
- Ensure compliance with regulatory requirements (e.g., FDA, EMA) and Good Clinical Practice (GCP) guidelines.
- Train and mentor junior CRAs and site personnel on study-specific procedures and requirements.
- Prepare monitoring reports and escalate site issues to project management promptly.
- Participate in the development of study protocols, Case Report Forms (CRFs), and other trial-related documents.
- Contribute to the overall success of clinical development programs by ensuring the integrity and quality of clinical trial data.
Qualifications:
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related healthcare field.
- Minimum of 5 years of experience as a Clinical Research Associate, with a significant portion dedicated to oncology trials.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Proven experience in site management, monitoring, and data collection.
- Excellent understanding of clinical trial processes and terminology.
- Strong organizational, time management, and problem-solving skills.
- Exceptional communication, interpersonal, and negotiation skills.
- Ability to work independently and manage multiple priorities effectively.
- Proficiency in electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- A commitment to ethical research practices and patient safety.
This hybrid position offers a dynamic work environment, blending remote flexibility with essential on-site engagement, providing a significant opportunity to contribute to life-saving cancer therapies.
This advertiser has chosen not to accept applicants from your region.
5
Senior Clinical Research Associate - Oncology
OX1 3AS Oxford, South East
£50000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company renowned for its commitment to developing life-saving therapies, is seeking a highly skilled Senior Clinical Research Associate (CRA) specializing in Oncology. This hybrid role offers the opportunity to contribute significantly to groundbreaking clinical trials, based in the vibrant city of Oxford, Oxfordshire, UK . You will be responsible for overseeing the conduct of clinical studies at investigator sites, ensuring compliance with protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Key Responsibilities:
- Manage and monitor assigned clinical trial sites to ensure the quality, integrity, and accuracy of data recorded.
- Conduct site initiation visits, interim monitoring visits, and close-out visits in accordance with study plans and regulatory requirements.
- Verify the accuracy and completeness of source documents and case report forms (CRFs).
- Ensure adherence to study protocols, standard operating procedures (SOPs), and applicable regulatory guidelines (e.g., ICH-GCP).
- Manage communication between study sites, the clinical study team, and the sponsor.
- Identify, track, and resolve site-level issues and deviations.
- Ensure timely reporting of adverse events (AEs) and serious adverse events (SAEs).
- Train and provide ongoing support to investigators and site staff on study-specific procedures.
- Participate in the selection and qualification of new clinical investigator sites.
- Contribute to the development of study protocols, clinical monitoring plans, and other study-related documents.
- Prepare and present monitoring visit reports and follow-up actions.
- Manage study supplies and investigational product accountability at assigned sites.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related scientific discipline. A Master's degree or higher is advantageous.
- Minimum of 5 years of experience as a Clinical Research Associate, with a significant focus on Oncology clinical trials.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements for clinical trials in the UK and Europe.
- Proven experience in site monitoring, data verification, and regulatory compliance.
- Excellent understanding of the drug development process and clinical trial phases.
- Strong organizational, time management, and problem-solving skills.
- Exceptional written and verbal communication skills, with the ability to build strong relationships with healthcare professionals.
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently and as part of a collaborative team in a hybrid work environment.
- Willingness to travel to assigned clinical sites as required.
This advertiser has chosen not to accept applicants from your region.
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6
Senior Clinical Research Associate (CRA)
OX1 1AA Oxford, South East
£50000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company renowned for its innovation in drug development, is seeking an experienced Senior Clinical Research Associate (CRA) to join their dynamic team. This role, based in the vibrant city of Oxford, Oxfordshire , operates on a hybrid model, offering a blend of remote flexibility and essential on-site presence for crucial study activities. You will play a pivotal role in overseeing clinical trials, ensuring adherence to protocols, regulatory requirements, and data integrity across multiple study sites. Your expertise will be instrumental in the successful execution of critical research studies aimed at bringing life-saving therapies to patients.
Key Responsibilities:
Key Responsibilities:
- Manage and monitor clinical trial sites to ensure compliance with study protocols, GCP, and regulatory guidelines.
- Conduct site initiation, interim monitoring, and close-out visits, documenting findings and ensuring timely resolution of action items.
- Build and maintain strong relationships with investigators, site staff, and other stakeholders.
- Ensure accurate and timely collection, verification, and submission of clinical data.
- Oversee drug accountability and manage investigational product at study sites.
- Identify, assess, and recommend potential new sites for clinical trials.
- Provide training and ongoing support to site personnel regarding study procedures and requirements.
- Contribute to the development and review of study-related documents, including protocols, case report forms (CRFs), and informed consent forms.
- Prepare and present study progress reports to internal teams and management.
- Ensure all activities are conducted in accordance with ethical principles and regulatory standards.
- Bachelor's degree in a life science, nursing, pharmacy, or related discipline. Advanced degree preferred.
- Minimum of 4-5 years of experience as a Clinical Research Associate, with a strong track record in monitoring clinical trials.
- Comprehensive knowledge of ICH-Good Clinical Practice (GCP) guidelines and other relevant regulatory requirements.
- Experience in various therapeutic areas is advantageous.
- Excellent understanding of clinical trial processes from site selection to close-out.
- Proficiency in clinical data management systems and electronic data capture (EDC) systems.
- Strong organizational, time management, and problem-solving skills.
- Excellent written and verbal communication skills, with the ability to communicate effectively with diverse stakeholders.
- Ability to work independently and as part of a team in a hybrid working environment, requiring regular presence in Oxford, Oxfordshire .
- Valid driver's license and willingness to travel to study sites as required.
This advertiser has chosen not to accept applicants from your region.
7
Experienced Clinical Research Associate, Sponsor Dedicated
Reading, South East
IQVIA
Posted 1 day ago
Job Viewed
Job Description
Our Sponsor Dedicated (cFSP) team is growing and we are looking for aspiring CRAs of all levels, join us on our mission to drive healthcare forward!
What We Offer / USPs
+ The chance to work on cutting edge medicines at the forefront of new medicines development
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
+ We offer genuine career development opportunities for those who want to grow as part of the organization
+ We invest in keeping our teams stable, so workload is consistent
+ As a CRA you will receive an iPad and use of key developments such as site visit app's, site visit report app's that allow CRA's to do their day job more efficiently
Responsibilities
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
+ If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis
+ If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement
Requirements
+ You should be life science degree educated
+ You have experience of independent on-site monitoring experience
+ You've handled multiple protocols and sites across a variety of drug indications
+ Flexibility and ability to travel
+ Strong communication, written and presentation skills
Awards
+ FORTUNE Magazine's World's Most Admired Companies list for the fourth year in a row - Ranked #1 in Its Category for the Fourth Consecutive Year
+ Best AI-based Solution for Healthcare" Award in 2023 Artificial Intelligence Breakthrough Awards
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
What We Offer / USPs
+ The chance to work on cutting edge medicines at the forefront of new medicines development
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
+ We offer genuine career development opportunities for those who want to grow as part of the organization
+ We invest in keeping our teams stable, so workload is consistent
+ As a CRA you will receive an iPad and use of key developments such as site visit app's, site visit report app's that allow CRA's to do their day job more efficiently
Responsibilities
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
+ If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis
+ If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement
Requirements
+ You should be life science degree educated
+ You have experience of independent on-site monitoring experience
+ You've handled multiple protocols and sites across a variety of drug indications
+ Flexibility and ability to travel
+ Strong communication, written and presentation skills
Awards
+ FORTUNE Magazine's World's Most Admired Companies list for the fourth year in a row - Ranked #1 in Its Category for the Fourth Consecutive Year
+ Best AI-based Solution for Healthcare" Award in 2023 Artificial Intelligence Breakthrough Awards
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
8
Experienced Clinical Research Associate, Sponsor Dedicated
Reading, South East
IQVIA
Posted 6 days ago
Job Viewed
Job Description
Our Sponsor Dedicated (cFSP) team is growing and we are looking for aspiring CRAs of all levels, join us on our mission to drive healthcare forward!
What We Offer
+ The chance to work on cutting edge medicines at the forefront of new medicines development
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
+ We offer genuine career development opportunities for those who want to grow as part of the organization
+ We invest in keeping our teams stable, so workload is consistent
+ As a CRA you will receive an iPad and use of key developments such as site visit app's, site visit report app's that allow CRA's to do their day job more efficiently
Responsibilities
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
+ If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis
+ If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement
Requirements
+ You should be life science degree educated
+ You have experience of independent on-site monitoring experience
+ You've handled multiple protocols and sites across a variety of drug indications
+ Flexibility and ability to travel
+ Strong communication, written and presentation skills
Awards
+ FORTUNE Magazine's World's Most Admired Companies list for the fourth year in a row - Ranked #1 in Its Category for the Second Consecutive Year
+ Best AI-based Solution for Healthcare" Award in 2023 Artificial Intelligence Breakthrough Awards
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
What We Offer
+ The chance to work on cutting edge medicines at the forefront of new medicines development
+ IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!
+ We offer genuine career development opportunities for those who want to grow as part of the organization
+ We invest in keeping our teams stable, so workload is consistent
+ As a CRA you will receive an iPad and use of key developments such as site visit app's, site visit report app's that allow CRA's to do their day job more efficiently
Responsibilities
+ Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
+ Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
+ Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
+ Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
+ Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
+ Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
+ Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
+ Collaborate and liaise with study team members for project execution support as appropriate
+ If applicable, may be accountable for supporting development of project subject recruitment plan on a per site basis
+ If applicable, may be accountable for site financial management according to executed clinical trial agreement and retrieve invoices according to local requirement
Requirements
+ You should be life science degree educated
+ You have experience of independent on-site monitoring experience
+ You've handled multiple protocols and sites across a variety of drug indications
+ Flexibility and ability to travel
+ Strong communication, written and presentation skills
Awards
+ FORTUNE Magazine's World's Most Admired Companies list for the fourth year in a row - Ranked #1 in Its Category for the Second Consecutive Year
+ Best AI-based Solution for Healthcare" Award in 2023 Artificial Intelligence Breakthrough Awards
**This role is not eligible for UK visa sponsorship**
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide.
To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.
EEO Minorities/Females/Protected Veterans/Disabled
This advertiser has chosen not to accept applicants from your region.
9