Latest Clinical Trial Manager jobs in Doylestown, PA

15 Clinical Trial Manager Jobs in Doylestown, PA

Clinical Research Coordinator SQRL - Plymouth Meeting, PA, United States Principal Investigator and Site Manager. While the PI and Site Manager are responsible for the overall design, conduct, and management of the clinical trial, you support, facilitate, and coordinate the daily 27 days ago
Manager, Site Operations (Clinical Trials - Annapolis, MD) Javara - Philadelphia, PA, United States , you will be responsible for comprehensive operational and relationship management of clinical trial activities associated with our healthcare partnerships. With a guiding principle of research participant safety 19 days ago
Associate Director Clinical Scientist, Oncology Merck - North Wales, PA 19454 - functional team members including clinical directors and study managers to lead/support clinical trial scientific activities. Job Responsibilities Responsible for the clinical/scientific execution of clinical 4 days ago
HEOR Project Manager----Remote US Tech Solutions - North Philadelphia, PA, United States , Patients, Prescribers, and Policy-makers. Provides HEOR strategic expertise under the supervision of the manager, to support clinical trial design and efficient implementation of HEOR-related contributions Yesterday
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Associate Director Clinical Research Insight Global - Philadelphia, PA, United States guidelines This person will train and supervise research staff, manage a portfolio of clinical trials, and oversees project managers 5 days ago
Sr. Director, Translational Medicine (GI) Johnson & Johnson - Spring House, PA and mentoring TMPLs (Associate Director and Director) who are accountable for developing early clinical development plans and executing clinical trials: from initial study design and continued monitoring USD 213,000.00 - 368,000.00 per year 4 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 12 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 14 days ago
Site Contract and Budget Specialist at ICON Clinical Research ICON Clinical Research - Blue Bell, Pennsylvania and Project Management in support of timely site start up for the conduct of clinical trials including accurate forecast of contract execution timelines. + Collaborates with the Functional Manager 4 days ago
Senior Clinical Scientist, Oncology Merck - North Wales, PA 19454 cross-functionally to monitor clinical data to ensure quality, completeness, and integrity of trial conduct. Providing tactical/scientific mentorship to other clinical scientists. Core Skills: Solid 20 days ago

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