Senior CRA

Senior CRA

 

The Sr. Clinical Research Associate manages clinical trials to ensure that trials are conducted in accordance with required regulations in the manner that is aligned with overall scientific goals and objectives.

Position plans clinical trial timelines, budgets, and resources needed to meet business goals and interfaces with employees from other departments and consultants in order to design and develop clinical plans, study materials, and related documentation.

This position includes preparation of clinical sections of required regulatory documents and day-to-day oversight of all aspects of trials including study start-up, monitoring, data management, analysis, and writing in house or through contract groups.

Basic Qualifications: Bachelors degree in a scientific discipline or equivalent required;
6 years of related oncology clinical research monitoring experience