Latest Clinical Data Management jobs in Raritan, NJ

92 Clinical Data Management Jobs in Raritan, NJ

Associate Director-Quality Assurance (QA-CMC) Clinical Dynamix - Raritan, NJ, United States disposition activities for manufactured products in support of clinical products, including MBR, EBR review, and approval and review of CoA. Responsible for Management and maintenance of the Veeva Quality Docs 14 days ago
Medical Director/ Sr. Medical Director, Clinical Development Johnson and Johnson - Raritan, NJ across the assigned study/studies within the clinical development program. • Work closely with functional partners (Data Management, Biostatistics, Regulatory, GCO, QMMC, GMS) to ensure an integrated 4 days ago
Director- Product Group Leader Johnson and Johnson - Raritan, NJ years of Product Management or similar experience is required in the pharmaceutical development IT (Clinical, Pharmacovigilance, and Regulatory) preferably focused on Clinical. * Proven hands 8 days ago
Lead Clinical Data Manager - Ethicon, Inc. Johnson & Johnson - Raritan, NJ at The Lead Clinical Data Manager (LDM) is responsible for all aspects of clinical data management associated with data cleaning and quality review processes for assigned trials with minimal supervision USD 105,000.00 - 150,000.00 per year 23 days ago
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Director Clinical Operations Johnson & Johnson - New Brunswick, NJ, United States and accountabilities are in place to achieve rapid, cost- effective and well executed clinical studies, for the supported franchises delivering high quality clinical data to support Regulatory, Market Access 6 days ago
Clinical Contract CRO RICEFW Technologies Inc - Parsippany, NJ, United States ) • Demonstrated ability to make critical decisions related to clinical vendor agreement negotiations and escalations • Consolidates data across functions according to business requirements and recommends vendors Yesterday
Director Toxicology Insmed Incorporated - Bridgewater, New Jersey , and interpretation of nonclinical safety data; and oversee nonclinical safety studies outsourced to contract research organizations. Provide strategic input to project teams and senior management regarding 6 days ago
Senior Director, Clinical Development (exclusive) Adecco - Elizabeth, NJ, United States for assigned clinical trials/programs (phase I - III). Develop protocols/amendments, provide medical monitoring of study conduct and oversight of patient safety, and provide medical support for data analysis Yesterday
Sr. Director, Global Drug Safety Adecco - Elizabeth, NJ, United States as you will need to travel to the NJ office 1 – 4 times a month (based on location). Responsibilities: Responsible for all safety data throughout the life cycle Lead safety signal surveillance and aggregate data Yesterday
Clinical SAS Programmer Katalyst Healthcares & Life Sciences - Bridgewater, New Jersey study-related documents produced by other functions (e.g. CRFs, Data Management Plan, SAPs, etc.) Create or review and approve CDISC-compliant datasets and corresponding documentation for electronic 7 days ago

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