654 Clinical Research Associates 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

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.

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

• 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.