On-Site Sponsor-Centric Clinical Research Monitor

A leading global healthcare provider is looking for a skilled Site Manager to perform monitoring and management of clinical studies in La Habra, California. The ideal candidate will have a Bachelor's Degree in a scientific discipline and at least 2 years of on-site monitoring experience. Responsibilities include site monitoring visits, protocol administration, and ensuring compliance with clinical practices. Strong communication, organizational skills, and knowledge of regulatory requirements are essential for success in this role.

An attractive salary range is offered based on qualifications.
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