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This role is not eligible remote, and must be onsite in one of our US office locations.
Accountable for the execution of assigned clinical studies/research collaborations from study design, through execution, to study close out. Additionally, responsible for initiation, oversight and completion of CES Ops continuous improvement and Strategic Imperatives workstreams. Oversight of the contract and budget execution, study timelines, study budget management, and ensuring study conduct is in accordance with Regeneron Standard Operating Procedures (SOPs), CES Ops Business Practice Tool processes and ICH/GCP, as applicable. The CES Ops portfolio is dynamic in nature; study types include less complex data transfer agreements, retrospective sample/data acquisition studies to more complex prospective studies including sample/data acquisition, biomarker/technology/method validation...