Senior Clinical Research Associate

Technical knowledge and experience managing most aspects of clinical studies

Experience in the pharmaceutical industry

Excellent knowledge of US and GCP/ICH regulations

Understanding of the clinical trials process, the application of SOPs, and medical terminology

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Corcept appreciates the commitment and hard work of all our team members as we strive to discover and develop novel treatments for patients with serious unmet medical needs.

Serves as a crucial member of the project team for the quality execution of assigned clinical protocols according to Corcept’s SOPs, ICH/GCP, and corporate and departmental program goals

Supports the Study Lead as an integral member of a multifunctional team to ensure clinical study activities including study start-up, enrollment, maintenance, and closeout are executed appropriately

Oversees some aspects of study management and vendors to ensure high quality of data

Participates in the review of study designs from an operations perspective, and site implementation tactics

May support Study Lead in the review of CRO/Vendor RFPs and participate in bid defenses and review and comment on proposals for vendor selection

Supports Study Lead in the development of study timelines and budgets per the corporate and departmental goals and continuously strives to ensure timelines and deliverables are met within budget