269 Clinical Research Associates jobs in the United Kingdom
Remote Clinical Research Coordinator
SW1A 0AA London, London
£35000 Annually
WhatJobs
Posted today
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Job Description
Our client, a pioneering biotechnology firm dedicated to advancing medical research, is seeking a meticulous and dedicated Remote Clinical Research Coordinator. This fully remote role offers the opportunity to contribute to groundbreaking studies from the convenience of your home. You will be responsible for the day-to-day management of clinical trials, ensuring adherence to protocols, regulatory guidelines, and ethical standards. This position requires exceptional organisational skills, a keen eye for detail, and a strong understanding of clinical research processes. You will play a vital role in bringing life-changing therapies to patients.
Key Responsibilities:
Key Responsibilities:
- Coordinating all phases of clinical trials, from initiation to close-out, ensuring compliance with study protocols.
- Recruiting, screening, and consenting study participants according to eligibility criteria.
- Managing study documentation, including case report forms (CRFs), source documents, and regulatory binders.
- Administering study-related procedures and collecting data accurately and efficiently.
- Monitoring participant adherence to protocols and managing adverse event reporting.
- Liaising with investigators, site staff, sponsors, and regulatory authorities.
- Maintaining data integrity and ensuring timely data entry into electronic data capture (EDC) systems.
- Managing study supplies, equipment, and laboratory samples.
- Ensuring compliance with Good Clinical Practice (GCP) guidelines and all applicable regulations.
- Communicating effectively with participants and providing them with necessary information and support throughout the trial.
- Bachelor's degree in a life science, nursing, or a related field.
- Minimum of 2 years of experience in clinical research coordination.
- Proficiency in understanding and applying clinical trial protocols.
- Familiarity with GCP guidelines and regulatory requirements (e.g., ICH).
- Experience with electronic data capture (EDC) systems.
- Strong organisational and time management skills.
- Excellent attention to detail and accuracy in data collection and record-keeping.
- Effective communication and interpersonal skills, with the ability to interact professionally with participants and healthcare professionals.
- Ability to work independently and manage responsibilities effectively in a remote setting.
- Basic knowledge of medical terminology and disease processes relevant to ongoing research.
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0
Remote Clinical Research Coordinator
BS1 3DQ Bristol, South West
£38000 Annually
WhatJobs
Posted 4 days ago
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Job Description
Our client, a pioneering force in healthcare innovation, is seeking a dedicated and highly organized Remote Clinical Research Coordinator to join their fully remote operations team. This position is crucial for the successful execution of clinical trials, supporting research professionals and participants from anywhere in the UK. You will be responsible for a wide range of administrative and operational tasks essential to the smooth running of research studies. Your duties will include managing study documentation, maintaining accurate participant records, coordinating study visits (virtually and, when necessary, facilitating in-person arrangements with local sites), and liaising with investigators, site staff, and study sponsors. A deep understanding of Good Clinical Practice (GCP) guidelines and relevant regulatory requirements is essential. The ideal candidate will possess exceptional organizational skills, meticulous attention to detail, and the ability to manage multiple tasks simultaneously in a remote work environment. Strong communication and interpersonal skills are vital for effectively interacting with diverse stakeholders, including patients, healthcare professionals, and research teams via virtual platforms. You will play a key role in ensuring data integrity, participant safety, and trial adherence to protocol. Experience with electronic data capture (EDC) systems and clinical trial management software is highly desirable. This role requires a proactive approach, excellent problem-solving capabilities, and the ability to work independently with minimal supervision. You will contribute to groundbreaking research aimed at improving patient outcomes and advancing medical knowledge. Opportunities for professional growth within a dynamic and supportive remote team are extensive. If you are passionate about healthcare research and thrive in a flexible, remote-first setting, this is an exceptional opportunity.Bristol, South West England, UK is the administrative base, but this role is 100% remote.
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1
Clinical Research Associate
London, London
Barrington James
Posted today
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Job Description
Job Title: Junior Clinical Research Associate (CRA) Location: London, UK (Field-based with regular site visits) Employment Type: Full-time About the Role: We are seeking a motivated Junior Clinical Research Associate (CRA) with a minimum of 2 years of independent monitoring experience to join our London-based team. The successful candidate will play a vital role in ensuring the quality and integrity of clinical trials across multiple therapeutic areas. You will conduct 4–6 monitoring visits per month , providing oversight of study sites while maintaining compliance with ICH-GCP, local regulations, and study protocols. Key Responsibilities: Perform routine monitoring visits (site initiation, interim, and close-out) across assigned sites in London and surrounding regions. Ensure adherence to protocol, ICH-GCP, and applicable regulatory requirements. Verify accuracy and completeness of case report forms (CRFs) against source data. Identify and resolve data discrepancies and protocol deviations in collaboration with site staff. Maintain effective communication with investigators, site personnel, and internal study teams. Prepare and submit timely monitoring reports and follow-up documentation. Support investigators and sites in resolving queries and ensuring readiness for audits and inspections. Contribute to trial start-up activities when required (e.g., site feasibility, essential document collection). Requirements: Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field. Minimum 2 years of independent monitoring experience within a CRO, pharmaceutical, or biotech environment. Strong knowledge of ICH-GCP and UK clinical trial regulations. Excellent organizational and time management skills with the ability to manage multiple sites. Willingness to travel frequently (4–6 site visits per month). Strong interpersonal and communication skills, both written and verbal. What We Offer: Competitive salary and benefits package. Professional development opportunities within a growing clinical operations team. Exposure to diverse therapeutic areas and phases of clinical development. Supportive work environment with mentorship from senior CRAs.
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2
Clinical Research Associate
London, London
Barrington James
Posted today
Job Viewed
Job Description
Job Title: Junior Clinical Research Associate (CRA) Location: London, UK (Field-based with regular site visits) Employment Type: Full-time About the Role: We are seeking a motivated Junior Clinical Research Associate (CRA) with a minimum of 2 years of independent monitoring experience to join our London-based team. The successful candidate will play a vital role in ensuring the quality and integrity of clinical trials across multiple therapeutic areas. You will conduct 4–6 monitoring visits per month , providing oversight of study sites while maintaining compliance with ICH-GCP, local regulations, and study protocols. Key Responsibilities: Perform routine monitoring visits (site initiation, interim, and close-out) across assigned sites in London and surrounding regions. Ensure adherence to protocol, ICH-GCP, and applicable regulatory requirements. Verify accuracy and completeness of case report forms (CRFs) against source data. Identify and resolve data discrepancies and protocol deviations in collaboration with site staff. Maintain effective communication with investigators, site personnel, and internal study teams. Prepare and submit timely monitoring reports and follow-up documentation. Support investigators and sites in resolving queries and ensuring readiness for audits and inspections. Contribute to trial start-up activities when required (e.g., site feasibility, essential document collection). Requirements: Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field. Minimum 2 years of independent monitoring experience within a CRO, pharmaceutical, or biotech environment. Strong knowledge of ICH-GCP and UK clinical trial regulations. Excellent organizational and time management skills with the ability to manage multiple sites. Willingness to travel frequently (4–6 site visits per month). Strong interpersonal and communication skills, both written and verbal. What We Offer: Competitive salary and benefits package. Professional development opportunities within a growing clinical operations team. Exposure to diverse therapeutic areas and phases of clinical development. Supportive work environment with mentorship from senior CRAs.
This advertiser has chosen not to accept applicants from your region.
3
Clinical Research Associate
Barrington James
Posted 2 days ago
Job Viewed
Job Description
Job Title: Junior Clinical Research Associate (CRA)
Location: London, UK (Field-based with regular site visits)
Employment Type: Full-time
About the Role:
We are seeking a motivated Junior Clinical Research Associate (CRA) with a minimum of 2 years of independent monitoring experience to join our London-based team. The successful candidate will play a vital role in ensuring the quality and integrity of clinical trials across multiple therapeutic areas. You will conduct 4–6 monitoring visits per month , providing oversight of study sites while maintaining compliance with ICH-GCP, local regulations, and study protocols.
Key Responsibilities:
- Perform routine monitoring visits (site initiation, interim, and close-out) across assigned sites in London and surrounding regions.
- Ensure adherence to protocol, ICH-GCP, and applicable regulatory requirements.
- Verify accuracy and completeness of case report forms (CRFs) against source data.
- Identify and resolve data discrepancies and protocol deviations in collaboration with site staff.
- Maintain effective communication with investigators, site personnel, and internal study teams.
- Prepare and submit timely monitoring reports and follow-up documentation.
- Support investigators and sites in resolving queries and ensuring readiness for audits and inspections.
- Contribute to trial start-up activities when required (e.g., site feasibility, essential document collection).
Requirements:
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
- Minimum 2 years of independent monitoring experience within a CRO, pharmaceutical, or biotech environment.
- Strong knowledge of ICH-GCP and UK clinical trial regulations.
- Excellent organizational and time management skills with the ability to manage multiple sites.
- Willingness to travel frequently (4–6 site visits per month).
- Strong interpersonal and communication skills, both written and verbal.
What We Offer:
- Competitive salary and benefits package.
- Professional development opportunities within a growing clinical operations team.
- Exposure to diverse therapeutic areas and phases of clinical development.
- Supportive work environment with mentorship from senior CRAs.
This advertiser has chosen not to accept applicants from your region.
4
Clinical Research Associate
London, London
Barrington James
Posted 2 days ago
Job Viewed
Job Description
Job Title: Junior Clinical Research Associate (CRA)
Location: London, UK (Field-based with regular site visits)
Employment Type: Full-time
About the Role:
We are seeking a motivated Junior Clinical Research Associate (CRA) with a minimum of 2 years of independent monitoring experience to join our London-based team. The successful candidate will play a vital role in ensuring the quality and integrity of clinical trials across multiple therapeutic areas. You will conduct 4–6 monitoring visits per month , providing oversight of study sites while maintaining compliance with ICH-GCP, local regulations, and study protocols.
Key Responsibilities:
- Perform routine monitoring visits (site initiation, interim, and close-out) across assigned sites in London and surrounding regions.
- Ensure adherence to protocol, ICH-GCP, and applicable regulatory requirements.
- Verify accuracy and completeness of case report forms (CRFs) against source data.
- Identify and resolve data discrepancies and protocol deviations in collaboration with site staff.
- Maintain effective communication with investigators, site personnel, and internal study teams.
- Prepare and submit timely monitoring reports and follow-up documentation.
- Support investigators and sites in resolving queries and ensuring readiness for audits and inspections.
- Contribute to trial start-up activities when required (e.g., site feasibility, essential document collection).
Requirements:
- Bachelor’s degree in Life Sciences, Nursing, Pharmacy, or related field.
- Minimum 2 years of independent monitoring experience within a CRO, pharmaceutical, or biotech environment.
- Strong knowledge of ICH-GCP and UK clinical trial regulations.
- Excellent organizational and time management skills with the ability to manage multiple sites.
- Willingness to travel frequently (4–6 site visits per month).
- Strong interpersonal and communication skills, both written and verbal.
What We Offer:
- Competitive salary and benefits package.
- Professional development opportunities within a growing clinical operations team.
- Exposure to diverse therapeutic areas and phases of clinical development.
- Supportive work environment with mentorship from senior CRAs.
This advertiser has chosen not to accept applicants from your region.
5
Clinical Research Associate
NR4 7TA Norwich, Eastern
£45000 Annually
WhatJobs
Posted 2 days ago
Job Viewed
Job Description
Our client, a leading pharmaceutical company, is seeking a dedicated Clinical Research Associate (CRA) to join their esteemed team. This hybrid role offers a blend of remote work flexibility and essential on-site responsibilities. As a CRA, you will play a pivotal role in the execution and oversight of clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards. This is an exciting opportunity to contribute to groundbreaking medical advancements within a supportive and professional environment.
Responsibilities:
Responsibilities:
- Plan, implement, and manage clinical trial activities at assigned sites.
- Conduct site initiation visits, interim monitoring visits, and close-out visits.
- Ensure compliance with Good Clinical Practice (GCP), regulatory guidelines, and study protocols.
- Verify the accuracy and completeness of clinical data through source data verification.
- Manage communication between the study sites and the sponsor organization.
- Identify and report adverse events and safety concerns promptly.
- Maintain essential study documents and site files.
- Train and support site staff on trial procedures and requirements.
- Monitor study progress and timelines, identifying and resolving potential issues.
- Contribute to the development of study protocols and case report forms.
- Prepare monitoring visit reports and follow up on action items.
- Bachelor's degree in Life Sciences, Nursing, Pharmacy, or a related field; advanced degree preferred.
- Previous experience as a Clinical Research Associate or in a similar clinical trial role.
- Thorough understanding of ICH-GCP guidelines and regulatory requirements for clinical trials.
- Experience with clinical trial monitoring and data verification.
- Excellent organizational, time management, and problem-solving skills.
- Strong interpersonal and communication skills, with the ability to build rapport with site personnel.
- Proficiency in medical terminology and understanding of disease processes.
- Ability to travel to clinical sites as required (estimated at 40-60%).
- Proficiency in using clinical trial management systems (CTMS) and electronic data capture (EDC) systems.
- A commitment to ethical research practices and patient safety.
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6
Clinical Research Nurse
Cornwall, South West
EmVenio
Posted today
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Job Description
Make a Difference on Your Own Schedule and Terms! Summary The Certified Mobile Research Nurse is a Registered Nursing ad-hoc/PRN position for EmVenio Clinical Research. Our CMRN is responsible for setting appointments within the required visitation window to complete mobile visits for study participants. You’ll work cooperatively with Clinical Project Managers, Coordinators, and site personnel to complete visits and submit accurate source documentation. We are looking for RGNs with current venepuncture and physical assessment competency to conduct visits with adult patients in their homes. The ability to drive with access to your own vehicle is a mandatory requirement for this position. Required Qualifications Full NMC registration with a minimum of two (2) years of experience as a Registered Nurse (RN) and no restrictions on practice Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw and Port access for administering infusions (date of last practice within 6 months, preferred) One (1) year of experience conducting full head-to-toe physical assessments, including using a stethoscope One (1) year of experience collecting vital signs, ECG, urine samples, and performing urine pregnancy tests Clean DBS Skilled at collecting accurate, detailed patient records including documentation of medical history and medication charting Excellent observational, verbal, written communication, and problem-solving skills Must have and maintain a current CPR certification Must have and maintain a current vaccination record Full, clean driving license with access to own vehicle Personal Incentives Gain GCP training certification Be a member of our general staffing pool with access to multiple study opportunities No research experience required, on the job training provided Contribute to advancements of truly life changing treatments Supporting the same patient throughout the trial, being on the cutting-edge of developing new groundbreaking treatments for a disease with high unmet need
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7
Clinical Research Nurse
Plymouth, South West
EmVenio
Posted today
Job Viewed
Job Description
Make a Difference on Your Own Schedule and Terms! Summary The Certified Mobile Research Nurse is a Registered Nursing ad-hoc/PRN position for EmVenio Clinical Research. Our CMRN is responsible for setting appointments within the required visitation window to complete mobile visits for study participants. You’ll work cooperatively with Clinical Project Managers, Coordinators, and site personnel to complete visits and submit accurate source documentation. We are looking for RGNs with current venepuncture and physical assessment competency to conduct visits with adult patients in their homes. The ability to drive with access to your own vehicle is a mandatory requirement for this position. Required Qualifications Full NMC registration with a minimum of two (2) years of experience as a Registered Nurse (RN) and no restrictions on practice Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw and Port access for administering infusions (date of last practice within 6 months, preferred) One (1) year of experience conducting full head-to-toe physical assessments, including using a stethoscope One (1) year of experience collecting vital signs, ECG, urine samples, and performing urine pregnancy tests Clean DBS Skilled at collecting accurate, detailed patient records including documentation of medical history and medication charting Excellent observational, verbal, written communication, and problem-solving skills Must have and maintain a current CPR certification Must have and maintain a current vaccination record Full, clean driving license with access to own vehicle Personal Incentives Gain GCP training certification Be a member of our general staffing pool with access to multiple study opportunities No research experience required, on the job training provided Contribute to advancements of truly life changing treatments Supporting the same patient throughout the trial, being on the cutting-edge of developing new groundbreaking treatments for a disease with high unmet need
This advertiser has chosen not to accept applicants from your region.
8
Clinical Research Nurse
Bristol, South West
EmVenio
Posted today
Job Viewed
Job Description
Make a Difference on Your Own Schedule and Terms! Summary The Certified Mobile Research Nurse is a Registered Nursing ad-hoc/PRN position for EmVenio Clinical Research. Our CMRN is responsible for setting appointments within the required visitation window to complete mobile visits for study participants. You’ll work cooperatively with Clinical Project Managers, Coordinators, and site personnel to complete visits and submit accurate source documentation. We are looking for RGNs with current venepuncture and physical assessment competency to conduct visits with adult patients in their homes. The ability to drive with access to your own vehicle is a mandatory requirement for this position. Required Qualifications Full NMC registration with a minimum of two (2) years of experience as a Registered Nurse (RN) and no restrictions on practice Two (2) years' experience in starting and performing Phlebotomy/Peripheral Blood Draw and Port access for administering infusions (date of last practice within 6 months, preferred) One (1) year of experience conducting full head-to-toe physical assessments, including using a stethoscope One (1) year of experience collecting vital signs, ECG, urine samples, and performing urine pregnancy tests Clean DBS Skilled at collecting accurate, detailed patient records including documentation of medical history and medication charting Excellent observational, verbal, written communication, and problem-solving skills Must have and maintain a current CPR certification Must have and maintain a current vaccination record Full, clean driving license with access to own vehicle Personal Incentives Gain GCP training certification Be a member of our general staffing pool with access to multiple study opportunities No research experience required, on the job training provided Contribute to advancements of truly life changing treatments Supporting the same patient throughout the trial, being on the cutting-edge of developing new groundbreaking treatments for a disease with high unmet need
This advertiser has chosen not to accept applicants from your region.
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