TANNER & ASSOC INC
Senior Manager Clinical Operations – San Francisco
TANNER & ASSOC INC, San Francisco, California, United States, 94199
Senior Manager Clinical Operations – San Francisco
New Position: Senior Manager Clinical Operations – San FranciscoTop tier Biotech company in the Bay Area is seeking a seasoned Senior Manger to oversee clinical trial operations. Duties will include project management, SOP development, CRO selection and management.Basic Requirements:5 to 8 years in the pharmaceutical/biotech industry including but not limited to 4 years overseeing trial management and 3 years of field monitoring experience conducting site qualification, initiation, routine, and close out monitoring visits.Oncology experience preferredCross-functional clinical project management skillsExcellent working knowledge of FDA & ICH/GCP regulations and guidelinesThorough knowledge of clinical monitoring proceduresExcellent analytical and assessment skillsExcellent judgment and problem solving skillsDemonstrated ability to develop and implement SOPs and Study PlansStrong experience working as a site monitor/Clinical Research Associate and thorough knowledge of clinical monitoring practices.
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New Position: Senior Manager Clinical Operations – San FranciscoTop tier Biotech company in the Bay Area is seeking a seasoned Senior Manger to oversee clinical trial operations. Duties will include project management, SOP development, CRO selection and management.Basic Requirements:5 to 8 years in the pharmaceutical/biotech industry including but not limited to 4 years overseeing trial management and 3 years of field monitoring experience conducting site qualification, initiation, routine, and close out monitoring visits.Oncology experience preferredCross-functional clinical project management skillsExcellent working knowledge of FDA & ICH/GCP regulations and guidelinesThorough knowledge of clinical monitoring proceduresExcellent analytical and assessment skillsExcellent judgment and problem solving skillsDemonstrated ability to develop and implement SOPs and Study PlansStrong experience working as a site monitor/Clinical Research Associate and thorough knowledge of clinical monitoring practices.
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