- Daiichi Sankyo, Inc. (Bernards, NJ)
- …be responsible for bringing the issue and potential solutions to the Head of US Regulatory Affairs in conjunction with the assigned US RA strategist on the ... ensuring consistent and transparent ways of working across the Alliance within US regulatory affairs and will work closely with the US Regulatory PMs… more
- Merck & Co. (Rahway, NJ)
- …monitoring, analysis, regulatory reporting, and publication. - Specifically, the Senior Director may be responsible for Evaluating pre-clinical and ... talented and dedicated colleagues while developing and expanding your career. - The Senior Director ( Senior Principal Scientist) has primary responsibility… more
- Merck & Co. (Rahway, NJ)
- …placement, monitoring, analysis, regulatory reporting, and publication.Specifically, The Senior Director May Be Responsible ForEvaluating pre-clinical and ... with talented and dedicated colleagues while developing and expanding your career.The Senior Director (Sr. Principal Scientist) has primary responsibility for… 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 ... cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting, and publication. -- Specifically, the Director may… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Executive Director , Global Pharma Communications is responsible for leading, developing and executing US and global communications strategies and ... Associate Vice President, Human Health and Manufacturing Communications, the Executive Director , Global Pharma Communications is responsible for the development of… more
- Merck & Co. (Rahway, NJ)
- … Senior / Executive Director group of experts in commercialization, regulatory affairs , statistics, medical affairs and manufacturing to manage ... areas regarding clinical issues related to oncology compounds.-The Executive Director /PDT lead may:-Manage Directors and/or Senior Directors responsible… 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 ... development projectsAssist the Senior Director , Associate Vice-President/Vice-President and Product Development Team Lead in ensuring that appropriate corporate… 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
- Daiichi Sankyo Inc. (Basking Ridge, NJ)
- …be responsible for bringing the issue and potential solutions to the Head of US Regulatory Affairs in conjunction with the assigned US RA strategist on the ... ensuring consistent and transparent ways of working across the Alliance within US regulatory affairs and will work closely with the US Regulatory PMs… more
- Bausch Health (Bridgewater, NJ)
- …it-where your skills and values drive our collective progress and impact. As a Senior Director in Health Economics and Outcomes Research (HEOR), you will be ... program teams, clinical development teams, market access, and medical affairs teams. + Providing a forum for global HEOR...matrix leadership teams + Thorough understanding of industry and regulatory guidelines as they relate to HEOR and Medical… more
- City of New York (New York, NY)
- …supervise and support the intergovernmental affairs workstream o Coordinate with senior leadership staff on legislative and regulatory matters impacting the ... Community Mental Health (OCMH) is seeking a Deputy Executive Director , External Affairs who will head the...projects and serve as a proxy for the Executive Director in senior level meetings, as needed… more
- Bristol Myers Squibb (Madison, NJ)
- …. The Medical Director , US Medical, Multiple Myeloma will report to the Senior Director , US Medical Multiple Myeloma Lead. He/she will be headquarter based, ... the US Commercialization organization, WW Medical, Clinical Research and Development, Regulatory , Translational Development, and Market Access, and will lead the US… more
- Merck (Rahway, NJ)
- **Job Description** **Job Scope** The Director , Corporate Affairs and Patient Innovation & Engagement Compliance has global compliance responsibility for all ... Corporate Affairs and Patient Innovation & Engagement leadership. The Director demonstrates subject matter expertise in relevant laws, regulations, policies, and… more
- LS Power Development, LLC (East Brunswick, NJ)
- …parental leave and more. **About the Role:** We currently have an opportunity for a Manager/ Director of Government Affairs that can be based in our New Jersey or ... and advocacy strategies.As a member of LS Power's government affairs team, you will be responsible for designing and...are clearly aligned with business + Communicate legislative and regulatory strategies clearly to senior and executive… more
- Mondelez International (East Hanover, NJ)
- …**Join our Mission to Lead the Future of Snacking. Make It Matter.** The Senior Manager, US Government Affairs will have responsibility for leading state ... affairs as part of the Corporate and Government Affairs (CGA) team. As Senior Manager, CGA,...and Global CGA team. This role reports to the Director , US Government Affairs , Mondelēz International. The… more
- System One (Florham Park, NJ)
- Job Title: Director / Senior Director , Medical Operational Excellence Lead Full time permanent position - Direct with a global pharmaceutical company Location: ... team. + Work closely with cross-functional teams, including medical affairs , clinical operations, regulatory affairs ,...-10 years ( Director ) or, minimum 10-12 years ( Senior Director ) of experience in medical operations,… more
- JPMorgan Chase (New York, NY)
- …years' experience at a large financial institution, regulator or law firm leading regulatory affairs and/or engagements. + BA/BS or similar degree required. + ... status quo and striving to be best-in-class. As a Regulatory Strategy Director within the Asset &...the team and offering strategic advice and direction to senior business/function leaders regarding regulatory matters. This… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …for all facing illness. As a senior member of Medical Science, the Senior Director , oncology group, Medical Science - Early Stage will lead the early-stage ... therapeutic areas involving complex indications including rare disease/orphan conditions. The Senior Director , oncology group, Medical Science - Early Stage… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …documents (ie protocols, Investigator's Brochures, clinical study reports, summaries for regulatory submissions). The Senior Director , Clinical Development ... Senior Director Clinical Development - Respiratory...as needed + Partners cross-functionally with departments such as Regulatory Affairs , Toxicology, CMC/Formulations, Biostatistics, Legal, Marketing,… more
- Merck (Rahway, NJ)
- …monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director may be responsible for** + Evaluating pre-clinical ... talented and dedicated colleagues while developing and expanding your career. **The Senior Director ( Senior Principal Scientist)** has primary responsibility… more
