- 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)
- …ethics-committees, and internal auditors in conjunction with CCQM, compliance, Regulatory ,-Pharmacovigilance (PV) and Medical Affairs .Responsible and supports ... Job DescriptionThe Clinical Research Director (CRD) is the Clinical Operations lead in...GCTO team (eg, salaries & travel).-Country level operational study budgets. Regulatory Inspections and internal audits; responding to inquiries by… 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)
- …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)
- … 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
- 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
- AbbVie (Jersey City, NJ)
- …The PST lead will also closely collaborate with a PK and toxicology leads, regulatory and clinical development leads as well as medical affairs colleagues to ... will be leading the safety components of pre-NDA and NDA/sNDA submissions, regulatory responses, label and label updates, RMPs. Responsibilities: + Understanding and… more
- NJEDA (Newark, NJ)
- …Staff, Managing Director - Policy, Research, and Government Affairs , and Director - Legislative & Regulatory Affairs to develop positions and ... contributes to bill comments prepared by the Legislative & Regulatory Affairs team on proposed legislation that...Senior Legislative Officer will report into the Managing Director - Policy, Research, and Government Affairs ,… more
