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Regulatory Compliance Officer
1 week ago
As a Clinical Research Associate at Biotech Healthcare, your primary responsibility will be to support clinical trials by ensuring compliance with regulatory guidelines and coordinating trial site activities.
Key tasks include:
- Preparing and submitting clinical trial-related documents to regulatory authorities
- Managing data collection, including data queries and discrepancies
- Liaising with investigators and other stakeholders to ensure timely data collection and resolution of site queries
Additional responsibilities may include performing source data verification and managing site visits to ensure compliance with Good Clinical Practice (GCP) guidelines.
We offer a competitive salary and benefits package to successful candidates who can demonstrate their ability to contribute to the success of our clinical trials program.
