544 Clinical Research Coordinator jobs in the United Kingdom

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

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

Join IQVIA as a Clinical Research Coordinator!

Are you passionate about clinical research and ready to make a real impact? Do you want to be part of a global leader in healthcare innovation? If so, we’d love to hear from you!

IQVIA is seeking a dedicated Clinical Research Coordinator to join our team in Torpoint , working 24 hours per week on a one year contract . This is a fantastic opportunity to contribute to cutting-edge clinical trials at a single site, supporting investigators and ensuring smooth study operations.

What You’ll Be Doing:

As a key member of the site team, you’ll play a vital role in supporting clinical research activities. Your responsibilities will include:

• Supporting clinical studies in line with health and safety policies under the guidance of the Principal Investigator.
• Maintaining study documentation including protocols, CRFs, and EDC systems.
• Coordinating logistics for study schedules.
• Assisting with data entry, quality checks, and resolving queries to ensure accuracy.
• Supporting patient recruitment and eligibility screening.

What We’re Looking For:

We’re seeking someone who is proactive, detail-oriented, and passionate about clinical research. Ideally, you’ll bring:

• At least 2 years’ experience as a Clinical Research Coordinator, Research Nurse, or Site Research Assistant.
• Solid understanding of clinical trials and study-specific procedures.
• Basic knowledge of medical terminology.
• Strong IT skills, including MS Office (Access, Outlook, Excel, Word).
• Excellent interpersonal and communication skills.
• Strong organisational abilities and attention to detail.

Why IQVIA?

At IQVIA, you’ll be part of a collaborative and forward-thinking team that’s shaping the future of healthcare. We offer a supportive environment, meaningful work, and the chance to grow your career in clinical research.

• 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.

• 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.

• 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.

• Coordinating all study-related activities, including patient recruitment, screening, scheduling, and follow-up visits.
• Obtaining informed consent from study participants and ensuring their understanding of study procedures.
• Collecting, documenting, and managing clinical data accurately and efficiently using electronic data capture (EDC) systems.
• Monitoring patient adherence to study protocols and reporting any adverse events or protocol deviations promptly.
• Maintaining comprehensive and organized study documentation, including regulatory binders and source documents.
• Liaising with investigators, research staff, sponsors, and regulatory authorities.
• Assisting with site initiation visits, monitoring visits, and close-out visits as required.
• Ensuring compliance with Good Clinical Practice (GCP) guidelines and other relevant regulations.
• Managing study supplies and investigational products.
• Educating patients and their families about the clinical trial.
• Participating in team meetings and contributing to the continuous improvement of clinical research processes.

• A Bachelor's degree in a life science, nursing, or a related healthcare field.
• Previous experience as a Clinical Research Coordinator or in a similar clinical research role.
• Thorough understanding of GCP guidelines, clinical trial processes, and regulatory requirements.
• Proficiency with EDC systems and other clinical trial management software.
• Excellent organizational, time management, and multitasking skills.
• Strong attention to detail and commitment to data accuracy.
• Exceptional interpersonal and communication skills, with the ability to interact professionally with patients, healthcare providers, and study sponsors.
• Ability to work independently and manage workload effectively in a remote environment.
• Strong problem-solving abilities and a proactive approach.