Clinical Research and Trainee Administrator

About the Role

Study Coordination: Assist in the identification, setup, administration, and monitoring of clinical trials (including

those from the NIHR portfolio and wider commercial sectors) including liaising with research nurses, sponsors, and

external partners. Data & Documentation Management: Accurately administer clinical trial data in compliance with Good

Clinical Practice (GCP), standard operating procedures (SOPs), and relevant regulations. Manage study documentation and

ensure adherence to regulatory requirements including liaising with the Data Protection Officer (DPO) if needed.

Participant Engagement: Serve as the initial point of contact for research participants, providing information and

Responsibilities

• Perform core duties as described.

Requirements

• Relevant experience or willingness to learn.

Benefits

• Benefits per job description.

Compensation

To be discussed.

Location & Schedule

Per job description.

How to Apply

Use the “Apply” button.