About the role
As a Clinical Research Coordinator, you will oversee the planning and execution of clinical trials. Your responsibilities will include recruiting and managing study participants, ensuring compliance with regulatory requirements, and collecting data accurately. This role is ideal for individuals with strong organizational skills and a passion for advancing medical research.
You will work closely with investigators and research teams, providing essential support in the coordination of studies. This position offers a unique opportunity to contribute to groundbreaking research while enhancing your career in the clinical field.
What you'll do
- Coordinate clinical trials and recruit participants
- Ensure compliance with regulatory standards
- Collect and manage data for research studies
- Collaborate with research teams and investigators
What you'll need
- Degree in Life Sciences or relevant field
- Experience in clinical research coordination
- Knowledge of Good Clinical Practice (GCP)
Skills
Strong organizational skills
Excellent communication skills
Detail-oriented approach
Good to have
Familiarity with clinical trial management software
Experience with patient interaction
Benefits
- Flexible working hours
- Health insurance
- Opportunities for professional growth
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?
They manage all aspects of clinical trials, including participant recruitment, compliance, and data collection.
Is this a remote position?
This role is hybrid, allowing for both onsite and remote work.
What experience is required?
A minimum of 2 years in clinical research is required.
What educational background is needed?
A degree in life sciences or a related field is preferred.
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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