- Merck & Co. (Rahway, NJ)
- …and/or PhD whose primary function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the regulatory approval ... Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and… more
- Insmed Incorporated (NJ)
- …future of science, we're in. Are you?About the Role:The Associate Director, Clinical Research Scientist will support and work predominately with the Medical ... with vendors and cross functional teams. This individual will provide scientific support to clinical development and operations, regulatory and quality assurance… more
- Merck & Co. (Boston, MA)
- … trials for investigational or marketed Atherosclerosis drugsAnalyzing and summarizing the clinical findings from studies to support decisions regarding safety ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
- Merck & Co. (Upper Gwynedd, PA)
- …the way we approach serious diseases. --The Senior Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the ... Director may be responsible for: -Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new… more
- Intuitive Surgical (Roanoke, VA)
- …VA Area to perform the duties of this role. Primary Function of Position The Clinical Territory Associate (CTA) is a 24+ month developmental role that will ... ways. We actively invest in our team members to support their long-term growth so they can continue to...in all aspects of our business to include technical, clinical , and sales. Essential Job Duties (Specific responsibilities and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good ... Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and other vendor… more
- Insmed Incorporated (San Diego, CA)
- …be responsible for the development and implementation of EDC systems to support clinical trials, ensuring data quality, compliance, and efficiency throughout ... and for the future of science, we're in. Are you?About the Role:The Associate Director, EDC Programming will lead and oversee EDC programming, and database build… more
- Novo Nordisk Inc. (Boulder, CO)
- …and Seattle reflect the full R&D continuum, from early research through late-stage clinical development. Here, we are building for the future, creating a distinct ... best of both worlds to develop new medicines for patients. The Position The Associate Director of Drug Product Manufacturing is accountable for all clinical drug… more
- ACROBiosystems Inc. (San Jose, CA)
- …in developing and manufacturing recombinant proteins and critical reagents/assays to support drug development and clinical applications from target discovery ... candidate drug screening and optimization, CMC development, preclinical and clinical studies, commercial production, and companion diagnostics. We are committed… more
- Merck & Co. (Rahway, NJ)
- …is responsible for the design and maintenance of statistical datasets that support multiple stakeholder groups which include clinical development, outcomes ... statistical programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and… more
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