654 Clinical Research Associates jobs in the United Kingdom
Clinical Research Coordinator
Posted 3 days ago
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Job Description
Clinical Research Coordinator (Part-Time) – Global CRO Client | Torpoint, Cornwall
Location: Torpoint, Cornwall
Hours: Part-time, 24 hours per week
Contract: 12-month contract
Pay Rate: £20–25 per hour
Start Date: ASAP
About the Role
We are partnering with a leading global Contract Research Organisation (CRO) to recruit an experienced and detail-oriented Clinical Research Coordinator (CRC) for an exciting part-time position based in Torpoint, Cornwall .
This is an excellent opportunity to contribute to high-quality clinical research within a respected global organization, supporting investigators and site teams in the delivery of pivotal studies that drive medical progress.
Key Responsibilities
- Coordinate day-to-day clinical trial operations in accordance with ICH-GCP, study protocols, and site SOPs.
- Schedule subject visits, manage patient study calendars, and send appointment reminders.
- Assist with patient prescreening, recruitment, and the informed consent process.
- Enter and verify study data in Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS) , ensuring accuracy and completeness.
- Maintain organized and compliant trial documentation, including regulatory and ethics submissions.
- Track study progress, resolve data queries, and support clear communication between site staff, monitors, and sponsors.
Candidate Requirements
- Minimum 1 year of experience as a Clinical Research Coordinator, Research Assistant, or in a similar research support role
- Working knowledge of clinical trial operations , regulatory standards, and GCP guidelines.
- Strong attention to detail , organizational, and multitasking abilities.
- Proficiency with Microsoft Office ; experience with EDC or CTMS systems is advantageous.
- Excellent interpersonal and communication skills , with a patient-focused and proactive approach.
- Background in life sciences, pharmacy, nursing, or biomedical research preferred.
Why Apply?
- Join a globally recognised CRO known for innovation and clinical excellence.
- Gain valuable hands-on experience across multiple therapeutic areas.
- Flexible part-time schedule and supportive team environment.
- Opportunity to make a direct impact on the success of vital clinical studies.
Clinical Research Coordinator
Posted 1 day ago
Job Viewed
Job Description
This is an exciting opportunity with candidates to start and interview as soon as possible!
The Clinical Research Coordinator must have minimum 1 year clinical research experience as they need an individual who can work independently as well as part of a team. Day to day responsibilities will involve data entry, query resolution and admin.
Bonus to have:
Experience with Oncology
Clinical Research Coordinator
Posted today
Job Viewed
Job Description
Clinical Research Coordinator (Part-Time) – Global CRO Client | Torpoint, Cornwall
Location: Torpoint, Cornwall
Hours: Part-time, 24 hours per week
Contract: 12-month contract
Pay Rate: £20–25 per hour
Start Date: ASAP
About the Role
We are partnering with a leading global Contract Research Organisation (CRO) to recruit an experienced and detail-oriented Clinical Research Coordinator (CRC) for an exciting part-time position based in Torpoint, Cornwall .
This is an excellent opportunity to contribute to high-quality clinical research within a respected global organization, supporting investigators and site teams in the delivery of pivotal studies that drive medical progress.
Key Responsibilities
- Coordinate day-to-day clinical trial operations in accordance with ICH-GCP, study protocols, and site SOPs.
- Schedule subject visits, manage patient study calendars, and send appointment reminders.
- Assist with patient prescreening, recruitment, and the informed consent process.
- Enter and verify study data in Electronic Data Capture (EDC) and Clinical Trial Management Systems (CTMS) , ensuring accuracy and completeness.
- Maintain organized and compliant trial documentation, including regulatory and ethics submissions.
- Track study progress, resolve data queries, and support clear communication between site staff, monitors, and sponsors.
Candidate Requirements
- Minimum 1 year of experience as a Clinical Research Coordinator, Research Assistant, or in a similar research support role
- Working knowledge of clinical trial operations , regulatory standards, and GCP guidelines.
- Strong attention to detail , organizational, and multitasking abilities.
- Proficiency with Microsoft Office ; experience with EDC or CTMS systems is advantageous.
- Excellent interpersonal and communication skills , with a patient-focused and proactive approach.
- Background in life sciences, pharmacy, nursing, or biomedical research preferred.
Why Apply?
- Join a globally recognised CRO known for innovation and clinical excellence.
- Gain valuable hands-on experience across multiple therapeutic areas.
- Flexible part-time schedule and supportive team environment.
- Opportunity to make a direct impact on the success of vital clinical studies.
Clinical Research Coordinator
Posted today
Job Viewed
Job Description
This is an exciting opportunity with candidates to start and interview as soon as possible!
The Clinical Research Coordinator must have minimum 1 year clinical research experience as they need an individual who can work independently as well as part of a team. Day to day responsibilities will involve data entry, query resolution and admin.
Bonus to have:
Experience with Oncology
Clinical Research Coordinator - Belfast
Posted 8 days ago
Job Viewed
Job Description
This role is to support the site in **Belfast** in conducting a clinical trial for **24** hours per week.
As a pivotal member of the site team, you will be involved with a variety of administrative tasks to support investigators and ensure the smooth running of clinical trials and assist with collecting patient data.
**Day to day responsibilities will include:**
+ Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
+ Safeguard the well-being of subjects, act as a volunteer advocate, and address subject's concerns
+ Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
+ Plan and coordinate logistical activity for study procedures according to the study protocol
+ Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
+ Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
+ Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
+ Correct custody of study drug according to site standard operating procedures
+ Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions.
**We are looking for candidates with the following skills and experience:**
+ Two years of experience with clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
+ Basic knowledge of medical terminology
+ Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
+ Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
+ Good organizational skills with the ability to pay close attention to detail.
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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.
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Senior Clinical Research Coordinator
Posted today
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Job Description
Key responsibilities include coordinating study visits, administering study-related procedures and assessments, and managing investigational products and study supplies. You will serve as a primary liaison between investigators, study participants, sponsors, and regulatory agencies, facilitating clear and consistent communication. The Senior Clinical Research Coordinator will also be involved in training and supervising junior research staff, ensuring the highest standards of research conduct. You will contribute to the development of study protocols, informed consent forms, and other essential research documents. Proactive identification and resolution of potential issues and challenges are crucial to the successful progression of clinical trials.
The ideal candidate will possess a Bachelor's degree in a health science-related field (e.g., Nursing, Pharmacy, Biology) or equivalent experience. A minimum of 5 years of experience as a Clinical Research Coordinator is required, with demonstrated experience in managing multiple complex trials. Strong knowledge of GCP, ICH guidelines, and relevant regulatory requirements (e.g., FDA, EMA) is essential. Excellent organizational, time management, and interpersonal skills are vital. The ability to work independently and as part of a collaborative team is key. This hybrid role offers the flexibility to work both remotely and from our facility near Birmingham, West Midlands, UK .
Remote Clinical Research Coordinator
Posted 5 days ago
Job Viewed
Job Description
Key Responsibilities:
- Recruit, screen, and consent study participants according to protocol eligibility criteria.
- Manage participant scheduling, appointments, and follow-up visits.
- Collect, document, and maintain accurate and complete study data in electronic data capture (EDC) systems.
- Process, label, and ship biological samples according to study-specific procedures.
- Administer study medication or interventions as directed by the principal investigator.
- Monitor participants for adverse events and report them promptly to the relevant parties.
- Maintain regulatory binders and study documentation, ensuring they are current and complete.
- Liaise with investigators, research staff, sponsors, and regulatory authorities.
- Participate in study initiation, monitoring, and close-out visits as required.
- Ensure compliance with all applicable regulations, guidelines, and ethical principles.
- Assist with protocol amendments, data queries, and the generation of study reports.
- Contribute to the continuous improvement of research processes and protocols.
- Effectively communicate with the research team and participants via virtual platforms.
- Bachelor's degree in a relevant scientific or healthcare field; Master's degree preferred.
- Minimum of 3-5 years of experience as a Clinical Research Coordinator or similar role.
- Thorough understanding of Good Clinical Practice (GCP) and other relevant regulatory guidelines.
- Proficiency in using EDC systems and other clinical research software.
- Excellent organizational, time management, and multitasking abilities.
- Strong attention to detail and commitment to data accuracy.
- Exceptional written and verbal communication skills.
- Ability to work independently and as part of a distributed team.
- Self-motivated with a proactive approach to problem-solving.
- Previous experience in a remote work environment is advantageous.
- Relevant certifications (e.g., ACRP, SoCRA) are a plus.
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Senior Clinical Research Coordinator
Posted 11 days ago
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Job Description
Key Responsibilities:
- Oversee the day-to-day operations of multiple clinical research studies from initiation to closure.
- Recruit, screen, and consent participants according to study protocols and ethical guidelines.
- Manage participant data, ensuring accuracy, confidentiality, and compliance with regulations (e.g., GDPR, HIPAA).
- Administer study medications, collect biological samples, and perform study-related procedures as required.
- Maintain meticulous study documentation, including source documents, case report forms (CRFs), and regulatory files.
- Liaise with principal investigators, sponsors, ethics committees, and regulatory authorities.
- Monitor study progress, identify potential issues, and implement corrective actions as needed.
- Ensure adherence to Good Clinical Practice (GCP) guidelines and all applicable research regulations.
- Coordinate study-related activities with healthcare professionals and external vendors.
- Prepare study reports, progress updates, and contribute to research publications.
The successful candidate will hold a relevant degree in a healthcare or life science discipline (e.g., Nursing, Biomedical Science) and possess a minimum of 5 years of experience as a Clinical Research Coordinator. A strong understanding of clinical trial phases, study design, and data management is essential. Experience with electronic data capture (EDC) systems and various research software is required. Excellent communication, interpersonal, and organisational skills are paramount, as is the ability to work autonomously and manage a demanding workload in a remote setting. Certifications such as ACRP or SoCRA are highly desirable. This role requires a compassionate individual with a commitment to patient welfare and the advancement of healthcare research within community settings.
Clinical Research Coordinator (Remote)
Posted 13 days ago
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Job Description
Job Description:
The Clinical Research Coordinator will manage the day-to-day operations of clinical trials, working closely with investigators, study participants, and sponsors. Your responsibilities will include screening potential participants, obtaining informed consent, coordinating study visits, collecting and processing data, and maintaining accurate trial documentation. This role demands a proactive approach, strong organizational skills, and a thorough understanding of Good Clinical Practice (GCP) guidelines.
Key Responsibilities:
- Screen potential participants for eligibility according to study protocols.
- Obtain and document informed consent from participants.
- Schedule and coordinate participant visits, ensuring protocol adherence.
- Collect, manage, and document study data accurately and efficiently, often via electronic data capture systems.
- Administer study medications or treatments as per protocol.
- Monitor participants for adverse events and report them promptly.
- Maintain comprehensive and accurate study files, including regulatory documents.
- Liaise with investigators, study sponsors, and regulatory authorities.
- Assist in preparing for site visits and audits.
- Ensure all research activities are conducted in compliance with GCP, ICH guidelines, and institutional policies.
- Bachelor's degree in a life science, nursing, or a related field.
- Proven experience as a Clinical Research Coordinator or similar role.
- In-depth knowledge of Good Clinical Practice (GCP) and regulatory requirements.
- Experience with electronic data capture (EDC) systems.
- Excellent organizational and time management skills.
- Strong attention to detail and accuracy.
- Effective communication and interpersonal skills, with the ability to build rapport with participants.
- Proficiency in Microsoft Office Suite.
- Ability to work independently and manage workload effectively in a remote setting.
- Certification as a Clinical Research Professional (e.g., ACRP, SoCRA) is a plus.
Remote Clinical Research Coordinator
Posted 16 days ago
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