About the role
In this role, you will manage clinical trial operations, coordinate with investigators, and ensure adherence to protocols. You will play a key role in recruiting and monitoring study participants, collecting data, and maintaining documentation for regulatory compliance. This position is suitable for experienced professionals with a passion for clinical research and a commitment to improving patient outcomes.
Our client offers a collaborative environment where you can contribute to groundbreaking research and make a difference in healthcare. If you are detail-oriented and thrive in a regulatory environment, we invite you to apply.
What you'll do
- Coordinate and oversee clinical trial operations.
- Recruit and monitor study participants.
- Ensure compliance with regulatory requirements.
- Collect and manage trial data and documentation.
What you'll need
- Bachelor's or Master's degree in life sciences.
- 3-5 years of experience in clinical research.
- Strong knowledge of clinical trial regulations.
Skills
Good to have
Benefits
- Opportunity to work on innovative research.
- Professional development opportunities.
- Collaborative team environment.
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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