Sr Associate, Clinical Research
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About The Position
The Senior Clinical Research Associate (Sr. CRA) will play a pivotal role in the clinical study life cycle, acting as a customer advocate and ensuring alignment with corporate goals. This position involves organizing and maintaining clinical study documentation, preparing for audits, and overseeing all aspects of study site monitoring. The Sr. CRA will be responsible for conducting pre-study and initiation visits, maintaining study files, and ensuring compliance with Good Clinical Practice (GCP) and regulatory requirements. Additionally, the role includes supporting the development of study-specific monitoring procedures, assisting in the selection and feasibility processes of study sites, and ensuring the integrity of data collected during the study. The Sr. CRA will also prepare trip reports, interact with internal groups, and support the revision and implementation of Clinical Affairs Standard Operating Procedures (SOPs). This position requires a strong commitment to patient safety and data integrity, as well as the ability to thrive in a fast-paced environment.
