Senior Clinical Research Associate – Romania
About the role
About Worldwide Clinical Trials
A global, midsize CRO with over 3,500+ experts committed to advancing clinical research and improving lives. We work with passion and purpose across diverse therapeutic areas including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
The Role
As a Senior Clinical Research Associate, you will manage research activities at sites participating in clinical research projects, predominantly registries and non-interventional/observational studies. You'll work alongside brilliant minds in a supportive, team-oriented environment with extensive support for regulatory submissions, TMF management, and site coordination.
Key Responsibilities
- Manage research activities at participating clinical research sites
- Identify potential sites and perform study start-up activities
- Collect appropriate regulatory documents and support contract and budget negotiations
- Train sites on proper data collection and safety event reporting
- Manage site activities during study maintenance phases
- Conduct study initiation visits (SIVs)
- Close down research activities at sites upon study conclusion
- Ensure compliance while performing predominantly remote site management
Why Join Us
We prioritize cultivating a diverse and inclusive environment that promotes collaboration and creativity. We are committed to enabling professionals from all backgrounds to succeed and thrive by being themselves while doing their best work.