About the role
As a Clinical Research Associate, you will be responsible for monitoring clinical trials, ensuring compliance with regulatory requirements, and maintaining accurate documentation. You will collaborate with healthcare professionals and researchers to facilitate the smooth operation of clinical studies. This role is ideal for a detail-oriented individual with a passion for improving healthcare outcomes through research. Our client offers a supportive team environment and opportunities for professional growth within the field.
What you'll do
- Monitor clinical trial sites for compliance with protocols
- Prepare and review study-related documents
- Coordinate with investigators and site staff
- Ensure timely reporting of study progress and outcomes
What you'll need
- Bachelor's degree in life sciences or related field
- Minimum of 2 years of experience in clinical research
- Knowledge of GCP and regulatory guidelines
Skills
Good to have
Benefits
- Opportunity to advance in clinical research field
- Collaborative and supportive work environment
- Professional development and training opportunities
Interested in this role?
It takes about two minutes. Free to apply — Callabri never asks candidates for money.
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