- Mitsubishi Chemical Group (Jersey City, NJ)
- …researching on real-world evidence, and creating hope for all facing illness. The Senior Director, Regulatory Affairs - Clinical (Neuroderm), may be ... plans to facilitate timely drug development and registration. The Senior Director, Regulatory Affairs -...current regulatory knowledge and provides guidance to regulatory staff and company management; identifies the… more
- NJEDA (NJ)
- Overview Job Summary Under the supervision of the Director of Legislative & Regulatory Affairs , the Senior Advisor supports all aspects of the duties of the ... Legislative & Regulatory Affairs Department, including but not limited...rulemaking efforts, receives and incorporates input from applicable program staff , Assistant/Deputy Attorneys General, Governor's Rules Office, other external… more
- AbbVie (Florham Park, NJ)
- …on Twitter, Facebook, Instagram, YouTube and LinkedIn. Job Description The Director Regulatory Affairs , Strategic Labeling is responsible for setting strategy ... or Microbiology + Preferred Education: Relevant Master's degree preferred. Certification in regulatory affairs a plus + Required Experience: 10+ years… more
- LS Power Development, LLC (East Brunswick, NJ)
- … strategies that are clearly aligned with business + Communicate legislative and regulatory strategies clearly to senior and executive leadership + Work closely ... currently have an opportunity for a Manager/Director of Government Affairs that can be based in our New Jersey...executing LS Power's legislative agenda and communicating it to senior management and other internal stakeholders. Priorities will be… more
- Veterans Affairs, Veterans Health Administration (East Orange, NJ)
- …timely recommendations. Participates with management in defending the budget before senior level management. Interacts and negotiates on adjustments or reprogramming ... influenza vaccination program is a requirement for all Department of Veterans Affairs Health Care Personnel (HCP). Participation in the Coronavirus Disease 2019… more
- Bristol Myers Squibb (Madison, NJ)
- …and other departments, including Commercial, Clinical Research and Development, Regulatory Affairs , Managed Care, Pharmacovigilance, Market Access, Statistics, ... Medical + Clinical Research and Development + Statistics + Translational Research + Regulatory Affairs including CMC- Regulatory + Manufacturing and Quality… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …required for senior management on a global basis. + Support regulatory safety reporting for clinical programs: SAE assessment, queries and follow-up, annual ... 2022. The company handles research, clinical development, sales, marketing, medical affairs , supply chain,and business development functions. MTPA is dedicated to… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …strong relationships with a wide range of stakeholders at all levels (eg, Senior Executive Team, board members, KOLs, regulatory bodies, investors, peers on ... 2022. The company handles research, clinical development, sales, marketing, medical affairs , supply chain,and business development functions. MTPA is dedicated to… more
- Gilead Sciences, Inc. (Trenton, NJ)
- …seeking a highly motivated individual to join our talented team as a Senior Medical Science Liaison (MSL). Kite MSLs are responsible for identifying, developing, and ... to a Regional Lead of MSLs within the Medical Affairs department. This role will support the New Jersey,...+ Work closely with other field-based employees and headquarters-based staff to rapidly respond to questions from sites in… more
- Edwards Lifesciences (Newark, NJ)
- …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you will drive the evidence needed to optimize… more
- Actalent (Atlantic City, NJ)
- …days on-site. + Must have phlebotomy proficiency + Must have knowledge of regulatory affairs --able to work independently as the primary/sole Clinical Research ... Job Title: Senior Clinical Research Coordinator 100% ONSITE role, +...in both Sponsor and Walgreens databases. * Supports the regulatory staff in the maintenance of … more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Director for Dermatology will lead a team of Medical Scientists to focus ... across all BMS functional and commercialization areas to ensure alignment. The Senior Director will report to the Executive Medical Director, SOTYKTU Lead **Key… more
- Bristol Myers Squibb (New Brunswick, NJ)
- …or product quality. + Collaborate with stakeholders, such as quality assurance, regulatory affairs , and site personnel, to gather additional information, discuss ... for efficiency improvements and resource optimization. Inspection Readiness and Regulatory Surveillance: + Review vendor inspection reports received from … more
- Bristol Myers Squibb (Princeton, NJ)
- …personal lives. Read more: careers.bms.com/working-with-us . Position Summary : Reporting to the Senior Direc tor , US and Above Market Medical and Market Access C&E ... Lead , this role partners with senior leaders across Legal, Commercial, Medical, R&D, Global Drug...leaders across Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory , IT, Audit, Finance and HR to build and… more
- Teva Pharmaceuticals (Parsippany, NJ)
- …cross-functional departments + Work closely with internal Teva departments such as Medical Affairs , Regulatory Affairs , and Supply Chain to address customer ... closely with internal teams-such as sales, marketing, and medical affairs -to align and implement effective strategies that drive product...a deep understanding of the LTC market and its regulatory environment, along with a proven track record in… more
- Integra LifeSciences (Princeton, NJ)
- …commercial, product development, process technology, operations, supply chain, procurement, regulatory affairs , finance, and human resources. + Communicate ... Device Regulations (CMDR), the EU Medical Device Regulation, Japanese Pharmaceutical Affairs Law, and other applicable regulatory agencies. **ESSENTIAL DUTIES… more
- Bristol Myers Squibb (Princeton, NJ)
- …of certain postmarketing commitments, and ensuring compliance with global regulatory requirements. **Position Summary** . Lead safety activities and benefit-risk ... documents as well as safety sections of relevant clinical trial documents and regulatory filings. . Lead team in the evaluation & management of signals emerging… more
- Bristol Myers Squibb (Princeton, NJ)
- …MS with general knowledge of pharmaceutical operations, ie, advocacy, medical affairs , clinical development, regulatory , commercialization. + Understanding of ... a high degree of interaction with teams encompassing Patient Advocacy, Medical Affairs , Research & Development, Commercialization, Corporate Affairs , and other… more
- Novo Nordisk (Plainsboro, NJ)
- …Hub. Key internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs , Data Management, Biostatistics, Non-clinical, Medical ... within the US East Coast Development Hub comprised of Senior Global Safety Leads, Global Safety Leads and ...teams. Oversees daily operations of the function by directing staff and adhering to company-wide policies, procedures and programs.… more
- Hackensack Meridian Health (Edison, NJ)
- …+ Minimum of 2 years experience in a Senior Clinical Data Coordinator or Senior Regulatory Specialist role, or at least 4 years related experience in the ... compliant study conduct according to all relevant local, federal, and state regulatory and institutional Polices and Standard Operating Procedures. This role carries… more