Salary: £32,424 pro rata per annum
Department: Clinical Research
Location: Liverpool
Hours: 37.5
Reports to: Site Manager
Job Summary
We are seeking a motivated and detail-oriented Clinical Trials Study Coordinator to join our research team. The successful candidate will be responsible for the day-to-day coordination and management of clinical trials in compliance with Good Clinical Practice (GCP), ethical guidelines, and regulatory requirements. This role is pivotal in ensuring the smooth running of trials and maintaining the highest standards of patient care and data integrity.
Main Duties and Responsibilities
- Coordinate the set-up, conduct, and closure of clinical trials.
- Act as a primary point of contact for sponsors, monitors, and regulatory authorities.
- Recruit, screen, and consent patients according to study protocols.
- Schedule and manage participant visits and follow-ups.
- Collect, record, and manage study data accurately in line with protocols.
- Monitor and report adverse events and ensure proper documentation.
- Maintain essential trial documents (Trial Master File / Investigator Site File).
- Assist in ethics and regulatory submissions and amendments.
- Collaborate with multidisciplinary teams including clinicians, research nurses, and data managers.
- Support audits and monitoring visits.
- Ensure compliance with GCP and institutional policies.
Person Specification
Essential:
- Degree in life sciences, healthcare, or a related field
- Minimum 6 months patient-facing experience
- Experience coordinating or supporting clinical trials
- Understanding of clinical research processes and ICH-GCP
- Excellent organisational and time management skills
- Strong communication and interpersonal skills
- Ability to work independently and as part of an MDT
Desirable:
- Evidence of post-registration study or research training
- GCP certification
- Experience with CTIMPs, oncology trials, or multi-centre studies
- Knowledge of MHRA, REC, HRA submissions
To apply for the position, please email hr@avrin.co.uk and and attach your CV
