Overview Location: Remote (If located in San Francisco role is hybrid) Contract: 6-12 Months (Asap Start Date) W2 Only The Opportunity We are working with an oncology-focused Biotech looking for an experienced data manager to help support in all aspects of the data management process like project documentation, UAT, and routine data review of trials. The initial contract will be 6-12 months, and the candidate must be on W2. Qualifications At least 3 years of CDM experience in pharma, biotech, or CRO, with some of that experience specifically in pharma or biotech Working understanding of ICH, FDA, and GCP regulations and guidelines Ability to handle multiple project tasks Web Based EDC experience and experience with MedDRA and WHO Drug Responsibilities Manage data management duties to meet study timelines Review appropriate protocols for data capture Provide DM support to statisticians and statistical programmers for clinical trial reports and other deliverables Perform scheduled and ad hoc data listing review and generate/solve queries in EDC Seniority level Mid-Senior level Employment type Contract Job function Science Industries Pharmaceutical Manufacturing and Biotechnology Research #J-18808-Ljbffr SciPro
Overview The Activities Director is responsible to plan, organize, develop, and direct the overall operation of the Recreation/ Activity Department in accordance with current federal, state, and local standards, guidelines and regulations, our established policies and procedures...
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