About the role
In this role, you will coordinate clinical studies, manage patient recruitment, and liaise with research staff to ensure compliance with regulatory standards. You will be responsible for documenting all trial-related activities and ensuring that data is collected accurately. This position is ideal for candidates with a strong background in clinical research looking to take the next step in their career. Our team is committed to advancing healthcare through innovative research, providing a supportive environment for professional growth.
What you'll do
- Coordinate clinical trials
- Manage patient recruitment
- Ensure compliance with regulatory standards
- Document trial activities accurately
What you'll need
- Degree in life sciences or related field
- 3-5 years of clinical research experience
- Strong communication skills
Skills
Good to have
Benefits
- Health insurance
- Professional development opportunities
- Flexible working hours
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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