- Merck & Co. (South San Francisco, CA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development ... Scientist) has primary responsibility for the strategic planning and directing clinical research activities involving investigational compounds in Immunology. With a… more
- Carnegie Mellon University (Pittsburgh, PA)
- …play a central role in coordinating these studies, analyzing outcomes, and preparing regulatory documentation in collaboration with clinical and regulatory ... a fully functional, immunocompetent, bioprinted human liver construct capable of clinical transplantation. Biofabrication is the heart of this mission, where… more
- Merck & Co. (Boston, MA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
- Insmed Incorporated (NJ)
- …documents across the lifecycle of inhalation products. Ensure alignment with regulatory guidance and clinical /commercial phase requirements.Contribute QC content ... of release, stability, and in-process testing in accordance with cGMP, regulatory requirements, and company quality standards. The successful candidate will provide… more
- Caris Life Sciences (Irving, TX)
- …+ Review marketing, promotional, and educational materials to ensure alignment with clinical data, regulatory guidelines, and Caris' strategic messaging. + ... Precision Oncology Alliance (POA). The Senior Medical Director will utilize their clinical depth, scientific acumen, and executive presence to shape and support… more
- Genmab (NJ)
- …Then we would love to have you join us!The RoleThe Senior Manager, Clinical Programming is responsible for the establishment, governance, and integrity of Study Data ... study or portfolio-level SDTM datasets are in compliance with CDISC and regulatory submission requirements, reviews study submission data packages to ensure quality… more
- BeOne Medicines (San Mateo, CA)
- …across the Pharma R&D value chain. By collaborating with stakeholders across Research, Clinical , Safety, Regulatory , Portfolio & Project Management and other R&D ... data products that address critical R&D use cases (eg, portfolio insights, clinical trial optimization, regulatory intelligence). + Establish best practices for… more
- Formation Bio (New York, NY)
- …than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
- Merck & Co. (North Wales, PA)
- …datasets, tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
- Alameda Health System (Oakland, CA)
- …team, responsible for providing strategic oversight of department-wide education, clinical competencies, quality assurance, regulatory compliance, PACS/RIS ... dashboards, quality scorecards, and performance reports to track metrics across regulatory , operational, and clinical domains. Use descriptive statistics and… more
