Latest Clinical Trials Manager jobs in Raritan, NJ

52 Clinical Trials Manager Jobs in Raritan, NJ

Senior Local Trial Manager - Immunology (1 of 3) Johnson and Johnson - Raritan, NJ . LTM) is responsible for local management of a clinical trial (or Medical Affairs data generation activity) in a country or countries. The Senior Local Trial Manager (Sr. LTM) is the primary point 5 days ago
Medical Director/ Sr. Medical Director, Clinical Development Johnson and Johnson - Raritan, NJ questions and HA presentations post-filing. • May review/co-author medical publications emerging from clinical trial results. • May act as a liaison between company and clinical investigators, vendor managers 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 27 days ago
Clinical Study Associate II Planet Pharma - Basking Ridge, NJ, United States , and International Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and other vendor performance against project goals 5 days ago
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Clinical Trial Manager Shiftcode Analytics, Inc - Basking Ridge, New Jersey CLINICAL TRIAL MANAGER 6+ MONTHS CONTRACT BASKING RIDGE, NJ / TARRYTOWN, NY HYBIRD (3 DAYS/WEEK) NEED IMMEDIATE JOINEE, START DATE Next week Monday VISA- NO CPT/H1B The Temp Senior Clinical Study 2 days ago
Clinical Trial Manager Shiftcode Analytics, Inc - Basking Ridge, New Jersey CLINICAL TRIAL MANAGER 6+ MONTHS CONTRACT BASKING RIDGE, NJ / TARRYTOWN, NY HYBIRD (3 DAYS/WEEK) NEED IMMEDIATE JOINEE, START DATE Next week Monday VISA- NO CPT/H1B The Temp Senior Clinical Study 3 days ago
Safety Case Management Product Specialist GForce Life Sciences - Princeton, NJ, United States . Responsible for configuring clinical studies in the database, review clinical trial protocols and configure reporting rules as per regulations. As Submissions SME, support local safety managers on daily basis 20 days ago
GPV Submission Specialist GForce Life Sciences - Princeton, NJ, United States . Responsible for configuring clinical studies in the database, review clinical trial protocols and configure reporting rules as per regulations. As Submissions SME, support local safety managers on daily basis 22 days ago
Clinical Trial Manager, Global Oncology Medical Affairs Daiichi Sankyo, Inc. - Bernards, NJ clinical activities. \r\n Process/Policies/Compliance Provide input to process standards and tools to achieve excellence in trial operations and management.Monitor and ensure compliance and highest quality 14 days ago
Trial Supplies Manager Ivory Systems - Summit, NJ, United States and external partners and customers. • Demonstrating strong knowledge when presenting clinical supply processes at cross-functional meetings and actively participates. • Ability to coach new Trial Supply 26 days ago

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