About the role
As a Clinical Research Associate, you will oversee the progress of clinical trials and ensure compliance with regulatory requirements. Your role will involve coordinating with research sites, monitoring trial progress, and collecting data. You will be responsible for preparing reports and ensuring the integrity of clinical data. This position suits professionals with strong organizational skills and a passion for advancing medical research.
What you'll do
- Monitor clinical trial activities
- Ensure compliance with regulatory guidelines
- Collect and analyze clinical data
- Prepare reports and documentation
What you'll need
- Bachelor's degree in Life Sciences
- Previous experience in clinical research
- Understanding of regulatory requirements
Skills
Strong analytical skills
Excellent communication
Detail-oriented
Good to have
Knowledge of clinical trial management software
Familiarity with GCP and ICH guidelines
Benefits
- Competitive salary
- Flexible work environment
- Opportunities for career advancement
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 typical day look like in this role?
You will spend your day monitoring clinical trials, ensuring compliance, and liaising with research sites.
Is a specific degree required for this position?
Yes, a degree in Life Sciences or a related field is necessary.
What is the duration of the contract?
The contract is initially for 12 months, with the possibility of extension.
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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