About the role
In this part-time role, you will coordinate clinical research projects, ensuring adherence to protocols and regulatory requirements. You will liaise with investigators, research staff, and patients to facilitate smooth operations of trials. The ideal candidate will have a background in life sciences and a keen interest in advancing medical research. Enjoy a flexible work environment that supports both professional and personal commitments.
What you'll do
- Manage clinical trial logistics
- Ensure compliance with ethical standards
- Maintain accurate trial documentation
- Coordinate communication between stakeholders
- Prepare reports and monitor trial progress
What you'll need
- Bachelor's degree in Life Sciences or related field
- Experience in clinical research preferred
- Knowledge of GCP and regulatory guidelines
Skills
Good to have
Benefits
- Work from home flexibility
- Professional development opportunities
- Supportive team and work culture
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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