On-Site Clinical Research Coordinator: Trials & Data
Green Life Science
Peterborough
On-site
GBP 30,000 - 45,000
Full time
14 days+
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Job summary
A clinical research organization in Peterborough is seeking a Clinical Research Coordinator to oversee clinical trials. This role involves coordinating trials from start to finish, recruiting participants, and ensuring compliance with GCP and other regulations. Ideal candidates will have previous experience in clinical research, strong organizational skills, and the ability to work effectively in a dynamic environment. Join a growing team focused on delivering results in clinical research.
Qualifications
Experience working in clinical research, preferably at the site level.
Good understanding of GCP and clinical trial processes.
Strong organisational and communication skills.
Comfortable working on-site in a fast-growing environment.
Previous experience as a Clinical Research Coordinator or Research Nurse.
Experience working across multiple studies or therapeutic areas.
Responsibilities
Coordinate and support clinical trials from start-up to close-out.
Screen, recruit, and schedule study participants.
Conduct study visits and collect trial data in line with protocol.
Maintain accurate study documentation and trial master files.
Liaise with investigators, sponsors, CROs, and monitors.
Ensure compliance with GCP, SOPs, and regulatory requirements.
Support monitoring visits, audits, and inspections.
Skills
Organisational skills
Communication skills
Understanding of GCP
Job description
A clinical research organization in Peterborough is seeking a Clinical Research Coordinator to oversee clinical trials. This role involves coordinating trials from start to finish, recruiting participants, and ensuring compliance with GCP and other regulations. Ideal candidates will have previous experience in clinical research, strong organizational skills, and the ability to work effectively in a dynamic environment. Join a growing team focused on delivering results in clinical research.