36 Researchers jobs in Oxford
Senior Research Associate
Oxford, South East
AbbVie
Posted today
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
Clinical Research Associate II
Reading, South East
IQVIA
Posted 7 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.
1
Experienced Clinical Research Associate
Reading, South East
IQVIA
Posted 19 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.
2
Experienced Clinical Research Associate
Reading, South East
IQVIA
Posted 19 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.
3
Clinical Research Associate (CRA)
RG1 7AL Reading, South East
£40000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a highly motivated and experienced Clinical Research Associate (CRA) to join their global team. This is a fully remote position, offering the opportunity to manage clinical trials across the UK from your home base. You will play a critical role in ensuring the quality, integrity, and efficiency of clinical studies, adhering to strict regulatory guidelines.
As a remote CRA, your primary responsibilities will include:
As a remote CRA, your primary responsibilities will include:
- Monitoring clinical trial sites to ensure adherence to protocol, Good Clinical Practice (GCP) guidelines, and regulatory requirements.
- Conducting site initiation visits, routine monitoring visits, and close-out visits.
- Verifying the accuracy, completeness, and consistency of clinical data collected at study sites.
- Ensuring timely reporting of adverse events and protocol deviations.
- Building and maintaining strong relationships with investigators, site staff, and study sponsors.
- Managing and maintaining essential study documents, including source documents and case report forms (CRFs).
- Identifying and resolving site-level issues and escalating them as necessary.
- Participating in study team meetings and providing updates on site performance.
- Ensuring the safety and well-being of study participants.
- Managing site budgets and timelines effectively.
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Associate (CRA)
RG1 2AL Reading, South East
£45000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client , a leading innovator in pharmaceutical research and development, is looking for a dedicated and meticulous Clinical Research Associate (CRA) to join their dynamic team in Reading, Berkshire, UK . This role offers a hybrid working model, blending essential on-site visits with the flexibility of remote work.
As a CRA, you will play a critical role in ensuring the successful execution of clinical trials by monitoring study sites and ensuring compliance with protocols, regulatory requirements, and good clinical practice (GCP). Your responsibilities will include:
The ideal candidate will have a Bachelor's degree in a life science, nursing, or a related field, with at least 2-3 years of direct experience as a CRA or in a similar clinical trial monitoring role. A strong understanding of ICH-GCP guidelines and regulatory requirements is essential. Excellent organizational, analytical, and interpersonal skills are required, along with the ability to work independently and manage multiple priorities. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is highly desirable. This hybrid role requires regular travel to clinical trial sites across the UK. If you are passionate about advancing medical treatments and ensuring the highest standards in clinical research, we encourage you to apply.
As a CRA, you will play a critical role in ensuring the successful execution of clinical trials by monitoring study sites and ensuring compliance with protocols, regulatory requirements, and good clinical practice (GCP). Your responsibilities will include:
- Performing site initiation visits, interim monitoring visits, and close-out visits to assess protocol and regulatory compliance.
- Verifying the accuracy, completeness, and quality of clinical data through source data verification (SDV).
- Ensuring investigational products are handled, stored, and dispensed correctly.
- Training and supporting site staff, including investigators and study coordinators.
- Identifying, escalating, and resolving site-level issues and deviations promptly.
- Preparing accurate and timely monitoring visit reports and action items.
- Maintaining effective communication with study sites, internal project teams, and regulatory authorities.
- Ensuring all trial-related documentation is maintained in the trial master file (TMF) and site files are current and complete.
- Contributing to the development and review of study protocols, case report forms (CRFs), and other study documents.
- Identifying potential risks to patient safety or data integrity and implementing mitigation strategies.
The ideal candidate will have a Bachelor's degree in a life science, nursing, or a related field, with at least 2-3 years of direct experience as a CRA or in a similar clinical trial monitoring role. A strong understanding of ICH-GCP guidelines and regulatory requirements is essential. Excellent organizational, analytical, and interpersonal skills are required, along with the ability to work independently and manage multiple priorities. Proficiency in clinical trial management systems (CTMS) and electronic data capture (EDC) systems is highly desirable. This hybrid role requires regular travel to clinical trial sites across the UK. If you are passionate about advancing medical treatments and ensuring the highest standards in clinical research, we encourage you to apply.
This advertiser has chosen not to accept applicants from your region.
5
Senior Clinical Research Associate (CRA)
OX1 1AA Oxford, South East
£60000 Annually
WhatJobs
Posted today
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is actively seeking a highly qualified and experienced Senior Clinical Research Associate (CRA) to join their esteemed research and development team. This position is entirely remote, allowing you to contribute to groundbreaking clinical trials from anywhere within the UK. As a Senior CRA, you will play a pivotal role in overseeing and managing various aspects of clinical trials, ensuring adherence to Good Clinical Practice (GCP) guidelines and regulatory requirements. Your primary responsibilities will include site selection, initiation, monitoring, and close-out visits to clinical trial sites. You will be responsible for verifying the accuracy and completeness of source data, ensuring data integrity, and managing regulatory documentation. Building and maintaining strong relationships with investigators and site staff will be crucial, providing them with guidance and support throughout the trial process. You will also identify and resolve site-specific issues, escalate any protocol deviations or safety concerns promptly, and contribute to the development and review of trial-related documents. The ideal candidate will possess a comprehensive understanding of clinical trial processes, a meticulous approach to detail, and exceptional organizational skills. Strong communication and interpersonal abilities are essential for effective collaboration with internal teams and external partners. This remote role demands a proactive, self-motivated individual who can manage their workload effectively and ensure the successful execution of clinical trials. You will be part of a global team dedicated to advancing medical science and bringing life-changing therapies to patients. A commitment to ethical research practices and patient safety is paramount.
Responsibilities:
Responsibilities:
- Conduct pre-study, initiation, monitoring, and close-out visits to clinical trial sites.
- Ensure compliance with protocols, ICH-GCP guidelines, and regulatory requirements.
- Verify source data and ensure accuracy of clinical trial documentation.
- Build and maintain strong working relationships with investigative sites.
- Identify, track, and resolve site issues and action items.
- Monitor subject recruitment and retention efforts.
- Oversee regulatory binder maintenance and study drug accountability.
- Communicate effectively with study team members, investigators, and site personnel.
- Bachelor's degree in a life science, nursing, or a related field; advanced degree preferred.
- Minimum of 5 years of experience as a Clinical Research Associate.
- In-depth knowledge of ICH-GCP guidelines and regulatory requirements.
- Proven experience in site monitoring and data verification.
- Excellent written and verbal communication skills.
- Strong organizational and time management skills.
- Ability to work independently and manage multiple priorities in a remote setting.
- Proficiency in EDC systems and CTMS.
- A commitment to patient safety and data integrity.
This advertiser has chosen not to accept applicants from your region.
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6
Clinical Research Associate (CRA) - Oncology
RG1 7LF Reading, South East
£40000 annum + ben
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a prominent global pharmaceutical company, is actively searching for a dedicated and experienced Clinical Research Associate (CRA) to support their vital oncology clinical trials. Based in Reading, Berkshire, UK , you will be responsible for monitoring clinical trial sites to ensure the accurate and efficient execution of studies in compliance with Good Clinical Practice (GCP), regulatory requirements, and internal company standards. Your core responsibilities will include site selection, initiation, routine monitoring (both on-site and remote visits, depending on study needs), and close-out visits. You will verify the quality and integrity of data collected, ensuring subject safety and protocol adherence. This involves reviewing case report forms (CRFs), source documents, and investigational product accountability. You will also build and maintain strong relationships with investigators and site staff, providing training and support as needed. Excellent organizational skills, meticulous attention to detail, and the ability to manage multiple tasks simultaneously are crucial. A Bachelor's degree in a life science, nursing qualification, or equivalent experience is required. Prior experience as a CRA, preferably within oncology or another complex therapeutic area, is essential, along with a thorough understanding of ICH-GCP guidelines and regulatory submission processes. Strong communication, problem-solving, and analytical skills are paramount. You must be able to work independently and as part of a team, demonstrating a proactive approach to identifying and resolving issues. This is an excellent opportunity to make a tangible impact on the development of life-saving cancer therapies.
This advertiser has chosen not to accept applicants from your region.
7
Experienced Clinical Research Associate, Sponsor Dedicated
Reading, South East
IQVIA
Posted 8 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 / 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
Remote Clinical Research Associate (CRA) - Oncology
OX1 3PA Oxford, South East
£45000 annum + car
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a prominent global Contract Research Organisation (CRO) at the forefront of clinical trial management, is seeking an experienced and meticulous Remote Clinical Research Associate (CRA) to focus on oncology studies. This fully remote position allows you to manage clinical trial sites across the UK from your home office, contributing to the development of life-changing cancer treatments. You will be responsible for monitoring study sites to ensure adherence to Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols. This role demands excellent organisational skills, a deep understanding of clinical trial processes, and the ability to build strong working relationships with investigators and site staff. You will play a vital role in ensuring the integrity and quality of clinical trial data, all within a flexible, remote working environment.
Key Responsibilities:
Key Responsibilities:
- Conduct site selection, initiation, monitoring, and close-out visits in accordance with study plans and SOPs.
- Ensure compliance with all study-specific protocols, GCP, FDA regulations, and ICH guidelines.
- Verify the accuracy, completeness, and integrity of clinical trial data through source data verification (SDV).
- Manage communication and relationships with study sites, investigators, and study coordinators.
- Identify and report adverse events and protocol deviations promptly.
- Train site staff on study procedures and ensure they have the necessary study materials.
- Monitor site performance and implement action plans to address any identified issues.
- Prepare monitoring visit reports and track site progress.
- Ensure timely data entry and query resolution from clinical sites.
- Maintain essential study documents and regulatory files.
- Participate in study team meetings and contribute to problem-solving discussions.
- Bachelor's degree in a life science, nursing, or related field.
- Significant experience (3+ years) as a Clinical Research Associate, with a strong focus on oncology clinical trials.
- Thorough understanding of GCP, ICH guidelines, and relevant regulatory requirements.
- Proven experience in conducting site monitoring visits and performing source data verification.
- Excellent clinical trial site management skills.
- Strong analytical, problem-solving, and organisational abilities.
- Exceptional written and verbal communication skills.
- Proficiency with clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- Ability to work independently and manage a remote workload effectively.
- A valid UK driving licence is required for site visits.
- Willingness to travel up to 60% of the time to study sites across the UK, starting from your home base, often near Oxford, Oxfordshire for local coverage.
This advertiser has chosen not to accept applicants from your region.
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