About the role
In this role, you will coordinate the day-to-day activities of clinical trials, including participant recruitment and data collection. You will ensure compliance with regulatory requirements and assist in maintaining documentation. This hybrid role offers flexibility, allowing you to work both onsite and remotely. The position is well-suited for candidates who thrive in a collaborative environment and are eager to contribute to the healthcare field.
What you'll do
- Coordinate clinical trials and manage participant recruitment
- Ensure compliance with regulatory requirements
- Maintain accurate documentation and data records
- Collaborate with research teams and stakeholders
What you'll need
- Bachelor's degree in Life Sciences or related field
- 1-3 years of experience in clinical research
- Strong organizational skills
Skills
Time management skills
Attention to detail
Effective communication skills
Good to have
Familiarity with clinical trial protocols
Basic statistical knowledge
Benefits
- Flexible work schedule
- Opportunity to work in medical research
- Access to training and development resources
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 will manage clinical trials, recruit participants, and ensure compliance with regulations.
Is this role part-time or full-time?
This position is part-time with a hybrid work model.
What qualifications do I need?
A degree in life sciences or related field along with relevant experience is preferred.
How do I apply for this job?
Click "Apply Now" on this page to apply through Callabri. Callabri is recruiting for this role on behalf of a client employer.
Listing last updated