Clinical Research Coordinator | Clinical Trials & Patient Engagement
Salary: £38,000 – £52,000 per year (commensurate with experience)
Location: Manchester or London (Hybrid flexibility – 2–3 days onsite per week)
Type: Full-Time
Industry: Healthcare Technology / Clinical Research / Biotechnology
Job Owner: Tariq Masood
Job Description
We are seeking a detail-oriented Clinical Research Coordinator (CRC) to oversee and manage clinical trial operations, ensuring strict adherence to Good Clinical Practice (GCP) guidelines, regulatory requirements, and study protocols.
In this role, you will coordinate all aspects of clinical research — from participant recruitment to data management and compliance monitoring — supporting the delivery of groundbreaking medical advancements and high-quality clinical outcomes.
This is an exciting opportunity to work at the intersection of healthcare innovation, patient care, and scientific research in a collaborative, fast-paced environment.
Experience
Minimum 2+ years in clinical research, ideally within a CRO, hospital, academic medical center, or biopharmaceutical setting.
Key Responsibilities
- Coordinate and manage the day-to-day operations of assigned clinical studies.
- Recruit, screen, and consent eligible study participants in accordance with IRB-approved protocols.
- Maintain accurate and up-to-date source documentation and electronic data capture (EDC) systems.
- Monitor patient safety, schedule study visits, and ensure strict protocol adherence.
- Liaise effectively with principal investigators, sponsors, and ethics committees.
- Prepare and manage regulatory documentation, site initiation, and close-out reports.
- Track study progress and provide timely updates to stakeholders and project teams.
- Ensure compliance with ICH-GCP, MHRA, and institutional regulations.
Required Skills
- Comprehensive knowledge of GCP, clinical research regulations, and ethical standards.
- Hands-on experience with clinical data collection, source documentation, and informed consent procedures.
- Proficiency in electronic data capture (EDC) systems (e.g., REDCap, Medidata, or equivalent).
- Strong organizational, time management, and documentation skills.
- Excellent communication and interpersonal abilities.
- Detail-oriented with the ability to manage multiple trials simultaneously.
Desired Skills
- Bachelor’s degree in Life Sciences, Nursing, or Health Sciences.
- ACRP or SOCRA certification preferred.
- Previous experience in oncology, cardiology, or rare disease clinical trials.
- Familiarity with clinical trial software platforms and regulatory submission processes.
Job Benefits
- Competitive salary with annual performance bonuses
- Training and career development opportunities in clinical operations and trial management
- Private health insurance and pension plan
- Supportive and flexible work environment
- Collaboration with a cross-disciplinary team of clinical and research professionals
Education
- Bachelor’s degree required; Master’s degree or clinical qualification preferred.
Additional Details
- Experience Required: Minimum 2 years in a clinical research setting
- Work Mode: Hybrid (2–3 days onsite per week)
- Sponsorship: Not considered
