About the role
As a Clinical Research Coordinator, you will oversee clinical trials and ensure compliance with regulatory requirements. You will manage participant recruitment, data collection, and liaise with research teams to ensure smooth operations. The ideal candidate should have strong organizational skills and a background in life sciences or healthcare.
This is an excellent opportunity for those who thrive in a fast-paced environment and are looking to make a significant impact in the clinical research field. You will be part of a supportive team committed to innovation and excellence in clinical trials.
What you'll do
- Oversee clinical trials
- Manage participant recruitment
- Ensure compliance with regulations
- Maintain study documentation
What you'll need
- Degree in life sciences or healthcare
- 2-5 years of experience in clinical research
- Strong organizational skills
Skills
Project management
Communication skills
Knowledge of clinical trial regulations
Good to have
Statistical analysis
Experience with electronic data capture systems
Benefits
- Competitive salary
- Professional development opportunities
- Collaborative work environment
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 are the main responsibilities of a Clinical Research Coordinator?
You will manage clinical trials, recruit participants, and ensure compliance with regulations.
What qualifications are required?
A degree in life sciences or healthcare and relevant experience in clinical research is needed.
What is the work environment like?
The position is onsite and requires collaboration with various teams in a clinical setting.
Is this a full-time position?
This is a contract position with the possibility of extension based on performance.
How do I apply for this role?
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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