Clinical Trials Manager

TN United Kingdom; Oxford; On-site; GBP 38,000 - 44,000; Full time

Job summary

A leading research center is seeking a Clinical Trial Manager to oversee multi-centre clinical trials at the John Radcliffe Hospital in Oxford. The role involves managing trial protocols, data entry, and supporting research practices. Candidates should have a degree in biomedical fields and experience in clinical research.

Qualifications

• Degree in biomedical or related fields or relevant experience in clinical research.
• Experience overseeing clinical trials and understanding of research governance.
• Proven administrative and project management skills.

Responsibilities

• Manage day-to-day operations of multi-centre randomized clinical trials.
• Finalize protocols and oversee data entry on the trial database.
• Provide advice and support to promote good research practice.

Skills

Project Management

Good Clinical Practice

Data Management

Education

Degree in Biomedical or Related Fields

Job description

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Position: Clinical Trial Manager

Location: Oxford Trauma and Emergency Care, Kadoorie Critical Care Research Centre, John Radcliffe Hospital, Oxford, OX3 9DU

Department: Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences (NDORMS)

Grade: 7

Salary range: £38,674 - £43,171 per annum (pro rata)

Contract: Full-time, fixed-term for 2 years; part-time at minimum 80% FTE considered

Job Description

We have an exciting opportunity for a Clinical Trial Manager to join the Oxford Trauma and Emergency Care group at the Kadoorie Research Centre. Based at John Radcliffe Hospital, Oxford, you will be responsible for the day-to-day management of multi-centre randomized clinical trials.

Your responsibilities include:

1. Finalizing protocols, study materials, and training packages for collaborating sites
2. Preparing trial-specific instructions
3. Overseeing data entry on the computer database, assisted by a Data Entry Clerk
4. Performing regular systematic checks of trial database information
5. Providing advice and support to colleagues internally and externally to promote good research practice

Qualifications and experience required:

• A degree in biomedical or related fields, or relevant experience in clinical research
• Experience overseeing clinical trials, working to high standards of Good Clinical Practice, and understanding of research governance
• Proven administrative and project management skills

Desirable:

• Previous experience as a trial coordinator/manager of multi-centre clinical trials
• Experience in developing clinical reporting forms