- Organon & Co. (Plymouth Meeting, PA)
- …questions per established business processes and systems. + Demonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the ... **Job Description** **The Position?** Reporting to the Director in Organon Regulatory CMC,?the Associate Principal Scientist is responsible for?developing… more
- Merck & Co. (South San Francisco, CA)
- …(including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations)Provide ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout… more
- Merck & Co. (Rahway, NJ)
- …the Final Study ReportMaintain contact with all stakeholders (project leader, regulatory affairs , quality assurance etc.) and keeps them informed ... include but are not limited to: The Associate Principal Scientist is a DVM and/or PhD whose primary function...clinical laboratory and field studies that will support the regulatory approval of new companion animal and livestock products.… more
- Merck & Co. (North Wales, PA)
- …studies.Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... Neuropathic Pain, Neuroscience, Neuroscience Research, Pain Management, Pharmaceutical Development, Regulatory Affairs Compliance, Regulatory Compliance,… more
- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionThe Principal Scientist /Director, Value & Implementation (V&I) Outcomes Research, position resides in the V&I organization, which includes Global ... Medical and Scientific Affairs as well as Outcomes Research.Under the guidance of...reimbursement and market access, and provides input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs.In… more
- Organon & Co. (Plymouth Meeting, PA)
- …questions per established business processes and systems. + Demonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the ... Regulatory Chemistry, Manufacturing and Controls (CMC), the Associate Principal Scientist is responsible for developing and implementing Regulatory Chemistry,… more
- Merck & Co. (MA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research activities… more
- Merck & Co. (North Wales, PA)
- …and executing integrated development plans that align clinical, medical affairs , commercial, manufacturing, regulatory , analytical, and epidemiological ... overseeing multiple studies and protocols through completionExperience in authoring regulatory documents and leading discussions with regulatory … more
- Post Holdings Inc. (Northfield, MN)
- …+ Conduct consumer and customer complaint investigations and report findings to consumer affairs group. + Work with Senior QFS Scientist to manage Food ... **Responsibilities** Our Northfield location is seeking a high caliber, motivated, self-driven scientist to join our Quality & Food Safety team. This role will… 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 ... Job DescriptionThe Senior Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing clinical research activities involving new or… more
- Organon & Co. (Plymouth Meeting, PA)
- **Job Description** **The Position** The Principal Scientist (Director) Regulatory Chemistry, Manufacturing and Controls is responsible for Regulatory ... for the assigned portfolio of small molecule or biologic products. The Principal Scientist may also support project team goals and organizational initiatives, on an… more
- Lilly (Indianapolis, IN)
- …to patients who need them all over the world. The Senior Advisor/Director Post approval scientist in Global Regulatory Affairs - CMC commercial solid oral ... strategies and submissions for Lilly's commercial solid oral products. The regulatory scientist will be encouraged to demonstrate innovative regulatory… more
- Mondelez International (East Hanover, NJ)
- …; Know Your Rights: Workplace Discrimination is Illegal **Job Type** Regular Scientific Affairs & Regulatory Affairs Product Quality, Safety and Compliance ... Future of Snacking. Make It With Pride.** The Sr. Scientist II will execute the Scientific Affairs ...respective categories and geographical area using your Scientific and Regulatory expertise. You advocate for our regulatory … more
- Lilly (Indianapolis, IN)
- …medicines to patients who need them all over the world. The Advisor Post approval scientist in Global Regulatory Affairs - CMC Commercial Products will ... regulatory strategies and submissions for Lilly's commercial products. The regulatory scientist will be expected to demonstrate innovative regulatory… more
- Hologic (San Diego, CA)
- Lead Clinical Affairs Scientist San Diego, CA, United States **Job Summary** The Lead Clinical Affairs Scientist is a highly visible role, leading ... Strong working knowledge of Good Clinical Practices (GCP), clinical research processes, and regulatory affairs . The annualized base salary range for this role is… more
- United Therapeutics (Research Triangle Park, NC)
- …part of a company that is forward thinking and innovative. The Senior/Statistical Scientist , Global Medical Affairs will contribute to all biostatistical and ... research and trends to inform statistical strategies Minimum Requirements Senior Statistical Scientist , Global Medical Affairs + Master's Degree in statistics or… more
- BD (Becton, Dickinson and Company) (Tempe, AZ)
- **Job Description Summary** The Staff Scientist , Scientific Affairs plays a key role in the development and execution of the evidence dissemination plan ... experience + Medical writing experience + Experience in cross-functional collaboration with regulatory , clinical, marketing, medical affairs , HEOR, and R&D +… more
- Veterans Affairs, Veterans Health Administration (Washington, DC)
- …Responsibilities The incumbent is a qualified and experienced clinical laboratory scientist (CLS) who supervises clinical laboratory scientists at the GS-9 and ... to cover typical workloads. Ensuring compliance with rules and regulations of assorted regulatory agencies such as the TJC, CAP, FDA, and the National Program… more
- Veterans Affairs, Veterans Health Administration (San Antonio, TX)
- …across multiple disciplines, evaluates and interprets results, and ensures regulatory compliance and data accuracy. Manages quality control, equipment calibration, ... with minimal direct oversight. Reports to the Supervisory Clinical Laboratory Scientist or Laboratory Manager. Works collaboratively with other laboratory staff to… more
- Veterans Affairs, Veterans Health Administration (Leeds, MA)
- …after complete review of the EDRP application. Responsibilities This Clinical Laboratory Scientist (Generalist) is in the Pathology and Laboratory Service at the VA ... at 40 hours per week. The GS-0644-7/9/11 Clinical Laboratory Scientist (Generalist) duties include but are not limited to:...laboratory procedures and results in line with current laboratory regulatory requirements. The work performed may be in a… more
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