About the role
As a Clinical Research Associate, you will oversee clinical trials, ensuring compliance with regulatory standards and protocols. Your role will involve monitoring trial progress, conducting site visits, and collaborating with investigators. This position suits candidates with a strong background in clinical research who are adept at data management and communication. If you thrive in a dynamic environment and have a passion for advancing healthcare, this role is for you.
What you'll do
- Oversee clinical trials
- Ensure regulatory compliance
- Conduct site visits
- Manage data collection and reporting
What you'll need
- Bachelor's degree in life sciences
- 3+ years of experience as a CRA
- Good clinical practice (GCP) knowledge
Skills
Strong analytical skills
Excellent communication
Attention to detail
Good to have
Familiarity with clinical trial management software
Project management skills
Benefits
- Flexible work hours
- Work from home
- Professional development training
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 key responsibilities of a Clinical Research Associate?
You will manage clinical trials, ensure compliance, monitor progress, and liaise with investigators.
Is this a remote position?
Yes, this position is fully remote.
What qualifications are required?
A degree in life sciences and relevant experience in clinical research is required.
How long is the contract period?
The contract is for 12 months with the possibility of extension.
What is the application process?
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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