- Merck & Co. (Boston, MA)
- …and Global Policy to ensure timely and equitable access to our medicines.The Senior Principal Scientist has primary responsibility for protocol development and ... and external leadership through interaction with key scientific leaders.Specifically, the Senior Principal Scientist is responsible for:Planning clinical trials… 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. (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. (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...pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.Specifically, The Senior Director… more
- Pfizer (Groton, CT)
- …and external partners, such as project leaders, research units, biostatistics, regulatory affairs , clinical pharmacology, human genetics, translational oncology, ... study reports (CSRs), investigator brochures, statistical analysis plans, and regulatory documents. Foster a transparent environment that builds strong partnerships… more
- Merck & Co. (Rahway, NJ)
- …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...including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director… more
- United Therapeutics (Research Triangle Park, NC)
- …excited to part of a company that is forward thinking and innovative. The Senior /Statistical Scientist , Global Medical Affairs will contribute to all ... abreast of latest research and trends to inform statistical strategies Minimum Requirements Senior Statistical Scientist , Global Medical Affairs + Master's… more
- Herbalife (Torrance, CA)
- …Apply Now **Overview** **POSITION SUMMARY STATEMENT:** The senior research scientist of NAM/MX scientific affairs will establish product efficacy and ... Sr. Research Scientist , Scientific Affairs Category: Research &...Nutrition product development efforts in NAM and MX. The senior research scientist will collaborate closely with… more
- Veterans Affairs, Veterans Health Administration (Manchester, NH)
- …complete review of the EDRP application. Responsibilities This Supervisory Clinical Laboratory Scientist is in the Pathology and Laboratory Service at the VA Medical ... is a full-time at 40 hours per week. GS-13 Supervisory Clinical Laboratory Scientist Assignment: The Supervisory Clinical Laboratory Scientist is responsible for… more
- Abbott (Santa Clara, CA)
- …device regulations and guidelines, and product and therapeutic area knowledge to support Regulatory Affairs medical device submissions in the EU for CE Marking ... and exchange of documents between stakeholders (eg, internal personnel such as Regulatory Affairs , R&D Engineering, Clinical Engineering, A&P and Marketing,… more
- Abbott (Santa Clara, CA)
- …with other departments including Global Clinical Operations, Research & Development, Regulatory Affairs , and Biostatistics. + Writes, study protocols, protocol ... regulatory agency meetings. + Works collaboratively with R&D, Clinical R&D, Regulatory Affairs , Library Services, Product Performance Group (PPG), Quality… more
- Merck (San Francisco, CA)
- …Global Policy to ensure timely and equitable access to our medicines. The Senior Principal Scientist has primary responsibility for protocol development and ... and external leadership through interaction with key scientific leaders. **Specifically, the Senior Principal Scientist is responsible for:** + Planning clinical… more
- J&J Family of Companies (Irvine, CA)
- …teams: medical affairs , data management, biostatistics, data programmers, and regulatory affairs + Ensure clinical research studies follow regulatory ... States of America **Job Description:** Johnson and Johnson is currently seeking a ** Senior Clinical Research Scientist ** to support the external research and… more
- Merck (Boston, MA)
- …scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations) + ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout… more
- Merck (Rahway, NJ)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Neuropathic Pain, Neuroscience, Neuroscience Research, Pain Management, Pharmaceutical Development, Regulatory Affairs Compliance, Regulatory Compliance,… more
- J&J Family of Companies (Spring House, PA)
- …Design, Process Hazard Analysis (PHA), Process Optimization, Program Management, Regulatory Affairs Management, Research and Development, Risk Management, ... Johnson & Johnson Innovative Medicine R&D is recruiting for a Senior Principal Scientist , Nonclinical Submissions Writer. This position is… more
- DEKA Research & Development (Manchester, NH)
- DEKA Research & Development has an immediate opening for a Biocompatibility & Toxicology Senior Scientist to join our team focused on medical device and ... this role will work directly with Research & Development, Regulatory & Clinical Affairs and Quality Engineering...will make a difference as a Biocompatibility & Toxicology Senior Scientist : + Work in close association… more
- AbbVie (North Chicago, IL)
- …. Job Description Purpose: We are looking for an experienced and versatile Senior Scientist II/Mechanical Engineer to join our Injection Device Development team ... course of our work, we collaborate with early-stage CMC, Quality Assurance, Regulatory Affairs , Internal and External Manufacturing, and other cross-functional… more
- Merck (North Wales, PA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... **Job Description** The Senior Director (Sr. Principal Scientist ) has...pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior … more
- Takeda Pharmaceuticals (Lexington, MA)
- …**Job Description** **Objective / Purpose:** We are seeking a highly motivated Senior Scientist to join the Potency and Functional Characterization team ... colleagues from Research, Quality Control, Process Development, Drug Product Development, and Regulatory Affairs to drive alignment on potency strategy and… more
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