About the role
In this role, you will coordinate clinical research projects, liaising with healthcare professionals and ensuring data integrity throughout the trial process. Your responsibilities will include monitoring patient recruitment, overseeing data collection, and preparing reports for regulatory submissions. This position requires a detail-oriented professional who thrives in a fast-paced environment and possesses strong communication skills. Join us to make a significant impact in the field of clinical research.
What you'll do
- Coordinate clinical trials
- Monitor patient recruitment
- Ensure data integrity
- Prepare regulatory submissions
What you'll need
- Degree in Life Sciences
- Experience in clinical research
- Knowledge of regulatory requirements
Skills
Strong communication
Attention to detail
Project management
Good to have
Experience with electronic data capture
Benefits
- Competitive salary
- Opportunity for professional growth
- Supportive work environment
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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Questions about this job
What are the main responsibilities of this role?
You will manage clinical trials, ensure compliance, monitor patient recruitment, and prepare regulatory submissions.
Is this a full-time or part-time position?
This is a contract position with full-time hours.
What qualifications are needed for this role?
A degree in Life Sciences or related field and prior experience in clinical research are required.
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