About the role
In this role, you will coordinate clinical research studies, ensuring compliance with regulations and protocols. You will be responsible for recruiting participants, collecting data, and collaborating with various departments to achieve study goals. This position suits professionals who are detail-oriented and possess strong organizational skills. You will work with a dedicated team committed to advancing medical research and improving patient health outcomes.
What you'll do
- Manage clinical trial protocols
- Recruit and screen study participants
- Collect and analyze trial data
- Maintain regulatory compliance
What you'll need
- Bachelor's degree in life sciences or related field
- Experience in clinical research management
- Good understanding of GCP guidelines
Skills
Excellent communication skills
Strong analytical skills
Proficiency in data management software
Good to have
Project management experience
Knowledge of clinical trial regulations
Benefits
- Competitive salary
- Flexible work hours
- Opportunity to work on innovative research projects
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 does a Clinical Research Coordinator do?
You oversee clinical trials, manage study protocols, and ensure regulatory compliance.
What qualifications are required for this role?
A degree in life sciences and previous clinical research experience are preferred.
Is this position remote or onsite?
This position is primarily remote with occasional onsite meetings.
How can I submit my application?
Click "Apply Now" on this page to apply through Callabri. Callabri is recruiting for this role on behalf of a client employer.
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