Freelance Clinical Research Associate
6 days ago
We are seeking an experienced Clinical Research Associate to join our team. As a CRA, you will be responsible for monitoring clinical trials within the local country.
- Regulatory submissions know-how is required.
- 5+ years of local monitoring experience.
- Medtech, pharma, and biologics background.
- Strong early-phase clinical trials experience.
- Solid ICH-GCP and local guidelines expertise.
- Bachelor's degree in a related field, advanced degree preferred.
Experience in the neurodegenerative or cardiovascular therapeutic area is a plus.
This is a freelance position, working full-time as a Clinical Research Associate based in the local country.
The ideal candidate will have a strong understanding of regulatory requirements and clinical trial procedures. If you are a detail-oriented individual with excellent communication skills, we encourage you to apply for this opportunity.
About the RoleThis role involves:
- Monitoring clinical trials in accordance with GCP and regulatory requirements.
- Maintaining accurate records and reports.
- Collaborating with cross-functional teams to ensure smooth trial execution.
This is a fantastic opportunity to work on high-profile clinical trials while developing your career as a Clinical Research Associate. You will have the chance to work with a talented team, learn from experienced professionals, and contribute to the success of our clients.
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