About the role
In this role, you will coordinate clinical trials, ensuring that all activities run smoothly and comply with regulatory requirements. You will work with research teams, monitor patient recruitment, and ensure data integrity throughout the study. This position is perfect for individuals with excellent organizational skills and a strong understanding of clinical research processes. You will act as a liaison between investigators, sponsors, and regulatory authorities, contributing to the advancement of medical knowledge and patient care.
What you'll do
- Coordinate and monitor clinical trials
- Ensure compliance with regulatory requirements
- Manage patient recruitment and retention
- Handle data collection and reporting
- Collaborate with research teams and stakeholders
What you'll need
- Degree in life sciences or nursing
- 2-4 years of experience in clinical research
- Strong organizational and communication skills
Skills
Good to have
Benefits
- Opportunity to work on cutting-edge research
- Health benefits
- Support for further education and training
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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