About the role
As a Clinical Trials Coordinator, you will manage the daily operations of clinical trials, ensuring adherence to protocols and regulations. You will work closely with investigators and study participants, coordinating schedules, and maintaining study documentation. This role is ideal for individuals with a strong background in clinical research and excellent organizational skills. Our client offers a supportive environment with opportunities for professional growth and development.
What you'll do
- Coordinate and manage clinical trial activities
- Ensure compliance with regulatory requirements
- Maintain accurate study documentation
- Liaise with investigators and participants
What you'll need
- Bachelor's degree in life sciences
- 2+ years of clinical research experience
- Knowledge of regulatory standards
Skills
Strong organizational skills
Excellent communication abilities
Attention to detail
Good to have
Experience with data management software
Familiarity with Good Clinical Practice (GCP)
Benefits
- Competitive salary
- Professional development opportunities
- Health insurance
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 this role?
You'll coordinate daily trial activities, manage documentation, and liaise with study participants.
Is this position full-time or part-time?
This is a contract position with full-time hours.
What qualifications do I need for this position?
A degree in life sciences and experience in clinical research are required.
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