Clinical Research Associate (CRA)
Armata Pharmaceuticals, Inc.
Clinical Research Associate (CRA)
Clinical Research Associate (CRA)
The Clinical Research Associate (CRA) will be responsible for the oversight and management of clinical trials, ensuring compliance with regulatory requirements and maintaining high standards of data quality and integrity. This role involves close collaboration with cross-functional teams, including project management, regulatory affairs, and clinical operations.
Key responsibilities include:
- Monitoring clinical trial progress and ensuring adherence to study protocols
- Conducting site visits and audits to verify compliance with regulatory and company standards
- Managing and coordinating study start-up activities, including site initiation visits and training
- Overseeing data collection, management, and reporting processes
- Providing training and support to site staff and study teams
- Ensuring timely and accurate reporting of adverse events and study progress
The ideal candidate will possess a strong background in clinical research, with a deep understanding of regulatory requirements and a commitment to excellence in clinical trial management.
Armata Pharmaceuticals, Inc.Vacancy posted 4 days ago
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