6,969 Clinical Research Professionals jobs in the United Kingdom
Clinical Research Associate/ Senior Clinical Research Associate
Barrington James
Posted today
Job Viewed
Job Description
About the Company
A fast-growing, tech-enabled CRO and global site network that started life within a major biopharma before becoming fully independent. They’ve built a proprietary AI platform now used to run smarter, faster clinical trials — and are expanding rapidly with their own hospitals and trial sites in India, and plans for Brazil, Australia, and China.
Now ~50 people, they’re closing Series A and moving into a Series B raise with a major bio-capital investor already signed. 0
It’s a genuine startup culture — everyone contributes, collaborates, and grows together. They also offer stock options from CRA level up – showing they invest in their people.
As their first UK CRA hire , you’ll have a key role in their European growth. You’ll monitor sites across the UK and EU (Spain, Greece, Italy, France, Germany) , support feasibility/start-up, and help shape the company’s operational foundations.
You’ll thrive here if you:
- Enjoy working autonomously in a small, fast-moving CRO.
- Want to help build something, not just follow a process.
- Can balance hands-on site work with cross-functional input.
What You’ll Need:
- 3 - 5 years CRA experience (CRO or sponsor)
- 5 - 7 years for a Senior CRA
- Proven EU monitoring exposure
- Solid knowledge of ICH-GCP & EU regs
- UK base with willingness to travel
- Startup or small-CRO experience is a big plus
- Oncology Based Experience
What’s on Offer:
- Competitive salary with higher flexibility for Senior CRA's
- Fast-track growth in a scaling, global business
- Exposure to AI-driven clinical operations
- Collaborative culture with true ownership and visibility
This advertiser has chosen not to accept applicants from your region.
0
Clinical Research Associate - Oncology Trials
NR3 1DZ Norwich, Eastern
£45000 Annually
WhatJobs
Posted 4 days ago
Job Viewed
Job Description
Our client, a rapidly expanding pharmaceutical company dedicated to advancing cancer treatments, is seeking a meticulous and experienced Clinical Research Associate (CRA) to join their team in Norwich, Norfolk, UK . This role offers a hybrid working arrangement, allowing for a balance between essential on-site monitoring and flexible remote work.
As a CRA, you will play a vital role in ensuring the successful execution of clinical trials, primarily focused on oncology indications. You will be responsible for site selection, initiation, monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) guidelines, study protocols, and regulatory requirements. Your dedication to data integrity and patient safety will be paramount.
Key Responsibilities:
As a CRA, you will play a vital role in ensuring the successful execution of clinical trials, primarily focused on oncology indications. You will be responsible for site selection, initiation, monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) guidelines, study protocols, and regulatory requirements. Your dedication to data integrity and patient safety will be paramount.
Key Responsibilities:
- Perform site visits (initiation, interim monitoring, and close-out) to assess trial conduct and ensure compliance with protocols, GCP, and regulatory standards.
- Verify accuracy, completeness, and consistency of data recorded in Case Report Forms (CRFs) and electronic data capture (EDC) systems.
- Monitor investigational product accountability and manage drug supply at study sites.
- Identify and report adverse events (AEs) and serious adverse events (SAEs) promptly.
- Build and maintain strong working relationships with investigators, site staff, and study sponsors.
- Ensure all necessary documentation is maintained in the Trial Master File (TMF).
- Provide training and ongoing support to study site personnel.
- Identify potential risks and issues at clinical sites and implement appropriate mitigation strategies.
- Contribute to the development of study protocols and other trial-related documents.
- Prepare and submit site visit reports in a timely and accurate manner.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field.
- A minimum of 3 years of experience as a Clinical Research Associate, with a strong focus on oncology trials.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Proven experience in conducting site monitoring visits and performing data verification.
- Excellent understanding of clinical trial processes and documentation.
- Strong organizational, time management, and prioritization skills.
- Exceptional communication, interpersonal, and negotiation skills.
- Proficiency in using EDC systems and clinical trial management software.
- Ability to travel to clinical sites as required (approximately 50-60%).
- Fluency in English, both written and spoken.
This advertiser has chosen not to accept applicants from your region.
1
Clinical Research Associate - Pharmaceutical Trials
CV1 1JH Coventry, West Midlands
£50000 Annually
WhatJobs
Posted 10 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company focused on developing life-changing medicines, is seeking a dedicated Clinical Research Associate (CRA) to join their team in Coventry, West Midlands, UK . This role offers a hybrid working arrangement, requiring a balance of remote work for administrative tasks and essential on-site visits to clinical trial sites. You will play a crucial role in ensuring the successful execution and monitoring of clinical trials, adhering to Good Clinical Practice (GCP) guidelines and regulatory requirements. Your responsibilities will include site selection, initiation, monitoring, and close-out visits to ensure data integrity, patient safety, and protocol compliance. You will serve as the primary point of contact for clinical trial sites, providing training and support to investigators and site staff. The ideal candidate will have a strong understanding of clinical trial processes, medical terminology, and regulatory frameworks governing pharmaceutical research. Previous experience as a CRA or in a similar clinical research role within the pharmaceutical or CRO industry is essential. Proficiency in EDC systems, CTMS, and other clinical trial management software is required. Excellent communication, organisational, and interpersonal skills are paramount, as is the ability to manage multiple sites and tasks effectively. A Bachelor's degree in a life science, nursing, or related discipline is necessary. This is a rewarding opportunity to contribute to the advancement of new therapies and build a successful career within a dynamic and collaborative pharmaceutical environment.
This advertiser has chosen not to accept applicants from your region.
2
Clinical Research Associate - Pharmaceutical Trials
BN1 1AA East Sussex, South East
£48000 Annually
WhatJobs
Posted 17 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a diligent and experienced Clinical Research Associate (CRA) to join their dynamic team in Brighton, East Sussex, UK . This role is instrumental in ensuring the successful execution of clinical trials according to Good Clinical Practice (GCP) guidelines and regulatory requirements. The CRA will be responsible for monitoring study sites, verifying data accuracy, and ensuring patient safety throughout the trial lifecycle. This involves conducting site initiation visits, routine monitoring visits, and close-out visits, as well as ensuring compliance with protocols and regulatory standards.
Key responsibilities include training site staff on study procedures, maintaining essential trial documents, and resolving data discrepancies in collaboration with investigators and site personnel. The successful candidate will possess excellent organizational skills, a keen eye for detail, and the ability to build strong working relationships with clinical sites and internal stakeholders. A solid understanding of drug development processes and clinical trial methodologies is essential. This hybrid role requires a balance of remote work for administrative tasks and site visits within the assigned territory. Travel will be a necessary component of this position. We are looking for a proactive, self-motivated individual with strong communication and problem-solving abilities. This is a fantastic opportunity to contribute to the development of life-saving medicines and advance your career within a globally recognized pharmaceutical organization.
Responsibilities:
Key responsibilities include training site staff on study procedures, maintaining essential trial documents, and resolving data discrepancies in collaboration with investigators and site personnel. The successful candidate will possess excellent organizational skills, a keen eye for detail, and the ability to build strong working relationships with clinical sites and internal stakeholders. A solid understanding of drug development processes and clinical trial methodologies is essential. This hybrid role requires a balance of remote work for administrative tasks and site visits within the assigned territory. Travel will be a necessary component of this position. We are looking for a proactive, self-motivated individual with strong communication and problem-solving abilities. This is a fantastic opportunity to contribute to the development of life-saving medicines and advance your career within a globally recognized pharmaceutical organization.
Responsibilities:
- Monitor assigned clinical trial sites to ensure adherence to protocols, GCP, and regulatory guidelines.
- Verify accuracy and completeness of clinical data through source document verification.
- Ensure patient safety and the rights of study participants are protected.
- Conduct site initiation, routine monitoring, and close-out visits.
- Train and support site staff on study-related procedures and requirements.
- Manage essential trial documentation and regulatory binders at site level.
- Identify, track, and resolve site-level issues and discrepancies.
- Liaise effectively with investigators, site staff, and internal project teams.
- Prepare detailed monitoring visit reports and follow-up actions.
- Contribute to the overall success of clinical trial execution.
- Life science degree or equivalent healthcare background.
- Proven experience as a Clinical Research Associate (CRA) or similar role.
- Thorough understanding of GCP, ICH guidelines, and regulatory requirements.
- Experience in monitoring various phases of clinical trials.
- Excellent organizational, time-management, and problem-solving skills.
- Strong interpersonal and communication skills, both written and verbal.
- Ability to travel regularly within the assigned region.
- Proficiency in clinical trial management software and electronic data capture (EDC) systems.
- Attention to detail and a commitment to data integrity.
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Associate
Reading, South East
IQVIA
Posted 14 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.
With access to world-class training and professional development, we'll give you the tools you need to create the career you want.
Do you want to know more about IQVIA? then see what Forbes said about us!
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!
*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.
With access to world-class training and professional development, we'll give you the tools you need to create the career you want.
Do you want to know more about IQVIA? then see what Forbes said about us!
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!
*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.
4
Clinical Research Associate
NE4 5BB Newcastle upon Tyne, North East
£40000 Annually
WhatJobs
Posted 1 day ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company based in **Newcastle upon Tyne**, is seeking an experienced Clinical Research Associate (CRA) to join their dedicated research team. This hybrid role offers a dynamic blend of on-site collaboration and remote flexibility, allowing you to contribute to groundbreaking medical advancements while maintaining a healthy work-life balance. As a CRA, you will be instrumental in the planning, implementation, and management of clinical trials, ensuring compliance with all ethical and regulatory standards. Your responsibilities will include site selection, initiation visits, routine monitoring, and close-out visits of clinical trial sites. You will verify the accuracy, completeness, and integrity of data collected during trials, working closely with investigators and site staff to resolve any issues or discrepancies. Strong attention to detail and an in-depth understanding of Good Clinical Practice (GCP) guidelines and relevant regulatory requirements (e.g., FDA, EMA) are essential. You will be responsible for ensuring that all trial-related documentation is maintained accurately and in a timely manner. The ideal candidate will possess excellent communication and organizational skills, with the ability to build strong working relationships with healthcare professionals. A Bachelor's degree in a life science, nursing, or related field is typically required, along with significant experience as a CRA. Experience with various therapeutic areas is a plus. You will travel to assigned clinical sites, often within the **Newcastle upon Tyne** region and potentially further afield, to ensure protocol adherence and data quality. This role requires a proactive approach to problem-solving and a commitment to patient safety and data integrity. You will report on trial progress, identifying potential risks and implementing mitigation strategies. The opportunity to work on innovative drug development projects and contribute to bringing life-changing therapies to patients makes this a highly rewarding position. Join a collaborative environment where your expertise will be valued and your career growth supported. This role requires meticulous record-keeping and adherence to strict protocols. You will participate in investigator meetings and provide training to site personnel as needed. A solid understanding of medical terminology and clinical trial procedures is a must.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate
NG1 1AA Nottingham, East Midlands
£38000 Annually
WhatJobs
Posted 18 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated Clinical Research Associate (CRA) to join their team in Nottingham, Nottinghamshire, UK . This hybrid role offers a blend of on-site and remote work, providing flexibility while ensuring critical project oversight. The CRA will play a vital role in ensuring the successful execution of clinical trials by monitoring study sites, verifying data accuracy, and ensuring compliance with protocols and regulatory guidelines (GCP, FDA, EMA). Responsibilities include site initiation visits, routine monitoring, close-out visits, and maintaining strong relationships with investigators and study staff. You will be responsible for ensuring that all trial-related documents are accurate, complete, and maintained meticulously. This role requires a proactive approach to problem-solving, identifying potential issues at study sites and implementing corrective actions swiftly. The ideal candidate will have a strong scientific background, typically a degree in a life science, nursing, or a related field, coupled with previous experience in clinical research or a similar role. Excellent understanding of ICH-Good Clinical Practice (GCP) guidelines and regulatory requirements is essential. Superior organizational skills, attention to detail, and effective communication abilities are paramount. You must be adept at working independently and as part of a larger team. Travel to study sites will be required as part of the role. This is an exceptional opportunity to contribute to groundbreaking pharmaceutical research and development in a supportive and forward-thinking organization.
This advertiser has chosen not to accept applicants from your region.
Be The First To Know
About the latest Clinical research professionals Jobs in United Kingdom !
6
Clinical Research Associate
SR5 2HH Sunderland, North East
£55000 Annually
WhatJobs
Posted 20 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated and meticulous Clinical Research Associate (CRA) to join their expanding operations in **Sunderland, Tyne and Wear, UK**. This hybrid role involves conducting site visits, monitoring clinical trial progress, and ensuring compliance with protocols, regulations, and Good Clinical Practice (GCP) standards. You will play a vital role in the successful execution of clinical studies, contributing to the development of life-saving medicines.
Key Responsibilities:
Qualifications:
Key Responsibilities:
- Conduct pre-study, initiation, routine monitoring, and close-out visits to clinical trial sites.
- Verify the accuracy, completeness, and compliance of clinical data and source documents.
- Ensure that all study-related activities are conducted in accordance with the study protocol, Investigator's Brochure, and applicable regulations.
- Train and support investigators and site staff on study procedures and requirements.
- Monitor patient recruitment and retention at study sites.
- Identify, document, and escalate site issues and discrepancies to the Clinical Operations Manager.
- Ensure timely submission of study-related documents and regulatory information.
- Build and maintain positive relationships with clinical investigators and site personnel.
- Prepare and present monitoring visit reports.
- Participate in the development of study protocols and Case Report Forms (CRFs) as needed.
Qualifications:
- Bachelor's degree in a life science, nursing, pharmacy, or related discipline; advanced degree preferred.
- Minimum of 3 years of experience as a Clinical Research Associate or equivalent role in the pharmaceutical or biotechnology industry.
- In-depth knowledge of GCP, ICH guidelines, and relevant regulatory requirements.
- Experience with electronic data capture (EDC) systems and clinical trial management systems (CTMS).
- Excellent understanding of medical terminology and clinical trial processes.
- Strong organizational, time management, and problem-solving skills.
- Exceptional written and verbal communication skills, with the ability to interact professionally with a variety of stakeholders.
- Ability to travel to clinical sites (approximately 50-70% travel may be required).
- Detail-oriented with a strong commitment to data integrity and patient safety.
- Proactive approach to identifying and resolving issues.
This advertiser has chosen not to accept applicants from your region.
7
Clinical Research Associate II/Senior Clinical Research Associate
Precision Medicine Group
Posted today
Job Viewed
Job Description
Precision for Medicine is not your typical CRO. We are passionate about cultivating our culture and are proud to share extremely high CRA retention rates compared to industry averages.
CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.
We are hiring a CRA II/Senior CRA, this position will be fully home based working in the UK.
About You
You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
Qualifications
Minimum Required:
Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.
We invite you to learn more about our growing organization serving our clients that are researching groundbreaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company.
Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice .
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at
It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
CRAs join us, love their jobs, and stay because of the amazing people and enjoyable quality of life. You will have a lower than average number of protocols, setting you up to be a protocol expert. Travel is reasonable and your work/life balance will benefit as a result. Most meaningfully - your voice will be heard. Working in a smaller CRO allows you to have influence and impact when it matters most and support from direct line management.
We are hiring a CRA II/Senior CRA, this position will be fully home based working in the UK.
About You
- You are calm, thoughtful, and responsive when things don’t go as planned.
- You are well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game.
- You find quick and creative ways of overcoming difficulties.
- You have an impeccable eye for detail.
- You identify potential study risks and propose solutions on how to mitigate them.
- You take responsibility in the quality and outcomes of your work.
- You are adept at handling conflict by using tried and true resolution strategies.
You will monitor and own the progress of clinical studies at investigative sites and ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards. You will coordinate all necessary activities required to set up and monitor a study (i.e., identify investigators; helping prepare regulatory submissions, conducting pre-study and initiation visits, etc.).
Qualifications
Minimum Required:
- 4-year college degree or equivalent experience
- Candidates should have at least 2 years CRA experience within the CRO or pharmaceutical industry.
- Oncology experience, early phase experience desirable although not essential.
- Availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment (international travel may be required for some senior level positions)
- Fluency in English
Precision medicine is revolutionizing the attack on cancer—and we are passionate about helping you harness its power. We strike tumors on a molecular level using biomarkers to link specific mutations to specific treatments. We combine deep science with deep data from advanced technological platforms, then layer on specialized expertise in the design and execution of targeted, adaptive clinical trials. Ultimately, we deliver robust insights that inform real-time decisions—and optimize the oncology development pathway.
We invite you to learn more about our growing organization serving our clients that are researching groundbreaking cancer therapies. We strive to ensure employees feel appreciated for the contributions they make every single day. You will provide input and have your ideas valued and nurtured, impacting positive change for the company.
Any data provided as a part of this application will be stored in accordance with our Privacy Policy. For CA applicants, please also refer to our CA Privacy Notice .
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
If you are an individual with a disability and require a reasonable accommodation to complete any part of the application process or are limited in the ability or unable to access or use this online application process and need an alternative method for applying, you may contact Precision Medicine Group at
It has come to our attention that some individuals or organizations are reaching out to job seekers and posing as potential employers presenting enticing employment offers. We want to emphasize that these offers are not associated with our company and may be fraudulent in nature. Please note that our organization will not extend a job offer without prior communication with our recruiting team, hiring managers and a formal interview process.
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Associate II or Senior Clinical Research Associate
Parexel
Posted 2 days ago
Job Viewed
Job Description
Parexel is in the business of improving the world's health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep conviction in what we do. We believe in our values, Patients First, Quality, Respect, Empowerment & Accountability.
**We are currently recruiting for Clinical Research Associate II and Senior Clinical Research Associate to join our Multi-Sponsor Clinical Trials Team in the UK.**
**This role if fully decentralised in the UK.**
**Your time here**
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA's are accountable for using their expertise to build and maintain the site relationship and ensure they're set up for success. As the clinical sites' sole point of contact, this includes addressing and resolving site issues and questions. You'll also manage site quality and delivery from site identification through to close-out.
As a CRA, Parexel will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, Parexel could be your next home.
**What you'll do**
+ Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
+ Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
+ Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
+ Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
+ Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
+ Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.
**More about you**
On your first day we'll expect you to have:
+ Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
+ Ability to perform all clinical monitoring activities independently.
+ Bachelor's or equivalent degree in biological science, pharmacy or other health related discipline.
+ Strong interpersonal, written, and verbal communication skills within a matrixed team.
+ Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
+ A client-focused approach to work and flexible attitude with respect to assignments/new learning.
+ The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
+ An honest and ethical work approach to promote the development of life changing treatments for patients.
+ Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.
**If you are ready to join Parexel's Journey, please apply!**
#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
**We are currently recruiting for Clinical Research Associate II and Senior Clinical Research Associate to join our Multi-Sponsor Clinical Trials Team in the UK.**
**This role if fully decentralised in the UK.**
**Your time here**
At Parexel, the CRA role offers the opportunity to go beyond the role of a typical clinical monitor. CRA's are accountable for using their expertise to build and maintain the site relationship and ensure they're set up for success. As the clinical sites' sole point of contact, this includes addressing and resolving site issues and questions. You'll also manage site quality and delivery from site identification through to close-out.
As a CRA, Parexel will offer you world class technology and training catered to your individual experience. You can anticipate less travel and a lower protocol load in comparison to industry peers. Your hard work may be rewarded through a bonus incentive program, the opportunity to work within multiple therapeutic areas and an opportunity to advance your career in clinical research. If impact, flexibility, and career development appeal to you, Parexel could be your next home.
**What you'll do**
+ Leverage your expertise. Conduct qualification visits (QV), site initiation visits (SIV), monitoring visits (MV) and termination visits (TV) at assigned clinical sites and generate visit/contact reports.
+ Build relationships. Oversee integrity of the study and utilize problem-solving skills to promote rapport with the site and staff.
+ Protect patients. Review the performance of the trial at designated sites, ensure the rights and well-being of human subjects are safeguarded and are in accordance with protocol.
+ Drive productivity. Develop patient recruitment strategies in conjunction with the clinical site to meet enrollment timelines, while also ensuring compliance with the approved standard operating procedures (SOPs), protocol/amendment(s), GCP, and the applicable regulatory requirement(s).
+ Ensure quality. Evaluate the quality and integrity of the reported data, site efficacy and drug accountability.
+ Execute. Monitor the completeness and quality of Regulatory Documentation and perform site document verification.
**More about you**
On your first day we'll expect you to have:
+ Site Management or equivalent experience in clinical research, with understanding of clinical trials methodology and terminology.
+ Ability to perform all clinical monitoring activities independently.
+ Bachelor's or equivalent degree in biological science, pharmacy or other health related discipline.
+ Strong interpersonal, written, and verbal communication skills within a matrixed team.
+ Experience working in a self-driven capacity, with a sense of urgency and limited oversight.
+ A client-focused approach to work and flexible attitude with respect to assignments/new learning.
+ The ability to manage multiple tasks, evaluate a variety of unpredictable scenarios and achieve project timelines while being able to apply your understanding of study protocol(s).
+ An honest and ethical work approach to promote the development of life changing treatments for patients.
+ Strong computer skills, including but not limited to the knowledge of a Clinical Trial Management System (CTMS), Electronic Document Management System (EDMS) and MS-Office products such as Excel and Word.
**If you are ready to join Parexel's Journey, please apply!**
#LI-REMOTE
EEO Disclaimer
Parexel is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to legally protected status, which in the US includes race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.
This advertiser has chosen not to accept applicants from your region.
9