- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Nordisk, you will have the opportunity to build a life-changing career in a global business environment. We encourage our employees to make the most of their talent, ... focusing on optimizing patient care and support. Relationships Reports to the Director of PSP Analytics and Ops Excellence. Key internal relationships include… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical Development, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …to seek alignment and share resources across multiple groups. Relationships Reports to Associate Director or above within CMR Training & Knowledge Management. ... About the Department The Clinical Development, Medical and Regulatory (CMR) department at Novo Nordisk is one...Collaborates with global and CMR leaders and stakeholders to develop comprehensive… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …in collaboration with global colleagues. Relationships Reports to the Associate Director Product Quality. Regularly interfaces with multiple NN Quality ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...maintained throughout the US supply chain Participates in various global product quality activities and projects Maintains up-to-date knowledge… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Regulatory Project Management and Strategic ... Regulatory Affairs Team. **How you will contribute:** + As Associate Director , Global Regulatory Project Management and Strategic Planning, you… more
- Ascendis Pharma (Princeton, NJ)
- The Regulatory Affairs (RA) Associate Director , Labeling will be responsible for labeling activities across programs and stages of development, with specific ... supporting global needs as required. The RA Associate Director , Labeling will be overall responsible...for regulatory submissions and product maintenance. The Associate Director prioritizes their own work to… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , Global Labeling Lead where you will be responsible ... You will serve as the regulatory expert for labeling on the Global Regulatory Affairs subteam to ensure that regulatory labeling requirements are met for… more
- J&J Family of Companies (Titusville, NJ)
- …- 2406187352W **Description** Johnson & Johnson Innovative Medicine is recruiting for an Associate Director Global Labeling Product Leader in Raritan, NJ; ... Associate Director , Global Labeling...experience. + Relevant experience in the pharmaceutical industry (eg, Regulatory Affairs, Clinical, Medical Information, Pharmacovigilance) including at least… more
- Merck (North Wales, PA)
- …with worldwide regulatory agencies and/or subsidiaries with regard to global regulatory strategy/registration requirements for one or more our company's ... submissions and associated documentation. + Provides expertise as the Global Regulatory Lead to Product Development Teams...but are not limited to:** + Reports to Executive Director or Associate Vice President, Therapeutic Area… more
- Publicis Groupe (Philadelphia, PA)
- …www.twitter.com/digitas_health **Job Description** Within Digitas Health, the Vice President, Director , Regulatory Review will provide advice to creative, ... review by Digitas Health's external clients. The Vice President, Director , Regulatory Review supports teams with managing...+ Manage multiple reports (direct or indirect) at the Director , Manager and Senior Associate level including… more
- Novo Nordisk (Princeton, NJ)
- …clinical development and regulatory requirements of a clinical program. The Associate Director will provide high level strategic input into development ... plans, study designs, and regulatory submissions. Relationships The Associate Director... global and local cross-functional study teams. The Associate Director should be seen as a… more
- Amicus Therapeutics (Princeton, NJ)
- …with Technical Operations, Regulatory and other internal partners, the EQL Associate Director is actively engaged in ensuring outsourced manufacturing is ... Associate Director , External Quality Lead (Small...External Quality Lead (Small Molecule) Amicus Therapeutics is a global , patient-dedicated biotechnology company focused on discovering, developing, and… more
- Merck (West Point, PA)
- …Health, Process Development, Commercialization, Operations, Technical Operations, Analytical, Quality, Regulatory -CMC, and Supply Chain. Associate Director ... **Job Description** **Position Description:** ** Associate Director ,** **Technology Transfer** **(TT)** **Systems...+ Demonstrated creative problem-solving skill. + Strong knowledge of global regulatory guidelines and cGMP principles. +… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , Clinical Pharmacology and Pharmacometrics - 2306103445W **Description** Janssen Research & Development, LLC is recruiting for an Associate ... right endpoint to achieve differentiation and develop a CP package that enables global product registration. + Accountable for all CP trial design, analysis of data,… more
- Merck (West Point, PA)
- … regulatory requirements, regulatory filings and company policies. The Associate Director also ensures that effective and robust Quality systems are ... **Job Description** The Associate Director , ESQL is responsible for...Quality Assurance and Quality Control including solid knowledge of global GMP and regulatory requirements. **OR** +… more
- J&J Family of Companies (Spring House, PA)
- Associate Director , Translational Clinical Medical Lead Translational Science & Medicine- Immunology - 2406188164W **Description** At Johnson & Johnson, we ... more at https://www.jnj.com/ . Johnson & Johnson is recruiting for an Associate Director , Translational Clinical Medical Lead (TCML), Immunology Translational… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , Clinical Pharmacology and Pharmacometrics - 2406183146W **Description** Johnson & Johnson Innovative Medicine is recruiting for an ... Associate Director , Clinical Pharmacology and Pharmacometrics, located...for the development of a compound, including interactions with regulatory agencies and functions as CPP Leader on the… more
- Merck (West Point, PA)
- …component of decision-making at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... Associate Director will work with scientists within...analyses + Developing and maintaining a comprehensive understanding of global regulatory expectations for small molecules and… more
- J&J Family of Companies (Horsham, PA)
- …skills and the ability to influence is necessary * Experience interacting with global regulatory authorities is also desirable * Approximately 20% travel ... Associate Medical Director , Rheumatology Therapeutic Area...products. She/he will partner with colleagues from Commercial, R&D, Global Medical Affairs, Real-world Value & Evidence, Biostatistics, and… more
