- Merck & Co. (Rahway, NJ)
- …studiesWork closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May… more
- Merck & Co. (Rahway, NJ)
- …studies;Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may be… more
- Bristol Myers Squibb (Madison, NJ)
- …MS or commensurate experience preferred **Experience Requirements** Significant experience in regulatory affairs (eg 3-5 years) **Key Competency Requirements** ... careers.bms.com/working-with-us . **Position Responsibilities** + Develop global and/or US regulatory strategy for Oncology products in development and through life… more
- AbbVie (Florham Park, NJ)
- …including Clinical Development Operations, Clinical Development, Biostatistics, Pharmacovigilance, and Regulatory Affairs , to ensure the integration and accuracy ... are 2 job openings: Director , Data Management Operations (Solid Tumor), Director , Data Management Operations ( Hematology ). Office locations: Lake County, IL,… more
- Bristol Myers Squibb (Madison, NJ)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The Medical Director , US Medical, Multiple Myeloma will report to the Senior Director ... the US Commercialization organization, WW Medical, Clinical Research and Development, Regulatory , Translational Development, and Market Access, and will lead the US… more
- AbbVie (Florham Park, NJ)
- …strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations, and emerging issues. ... of scientific content of protocols, Investigator Brochures, Clinical Study Reports, regulatory submissions and responses, and other program documents. *May oversee… more
- Merck (Rahway, NJ)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, The Senior Director … more
- Bristol Myers Squibb (Madison, NJ)
- …and other departments, including Commercial, Clinical Research and Development, Regulatory Affairs , Managed Care, Pharmacovigilance, Market Access, Statistics, ... Research and Development + Statistics + Translational Research + Regulatory Affairs including CMC- Regulatory +...7+ years of clinical experience: including specific expertise in hematology /oncology as well as, medical affairs or… more
- Danaher Corporation (New York, NY)
- …diagnostic tools that address the world's biggest health challenges. The Medical Director , Scientific and Medical Affairs position for Beckman Coulter ... that improve patient care. You will be a part of the Medical and Scientific Affairs team and report to the Senior Director , Medical and Scientific Affairs… more
- Merck (Rahway, NJ)
- …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... cycle of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. Specifically, the Director may be… more
