- Genmab (Plainsboro, NJ)
- …and authentic is essential to fulfilling our purpose.The RoleGenmab is looking for an Associate Director , Global Regulatory Affairs, Regulatory Strategy ... to be a part of our Global Regulatory Affairs organization.In this role, you will work in...of the Company Core Data Sheep and US Prescribing Information . Responsible for maintenance of the IND. Monitor and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …lives for a living. Are you ready to make a difference? The Position The Associate Director , Regulatory Affairs - Advertising & Promotion will provide ... strong and positive working relationship with OPDP reviewers. Report to Senior Director , Regulatory Affairs - Advertising & Promotion. Essential Functions… more
- Merck & Co. (North Wales, PA)
- …/Senior Director in the Office of Promotion and Advertising Review (OPAR)The Associate Director is responsible for the review and approval of all US ... promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to...or other applicable legally protected characteristics. - For more information about personal rights under the US Equal Opportunity… more
- Genmab (Plainsboro, NJ)
- …our best, and authentic is essential to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager/ Associate Director will be ... Core Data Sheet, USPI, EU SmPC and related patient information ) for the Genmab portfolio of products. This role...portfolio of products. This role will be within Global Regulatory Affairs (GRA) and will report to the Sr… more
- Genmab (Plainsboro, NJ)
- …be our best, and authentic is essential to fulfilling our purpose.The RoleThe Associate Director , Digital Strategy - Medical/Access/PSS & Paid Media will serve ... media efforts in the US. This critical role reports directly to the Senior Director of Digital Strategy and will be expected to work across assigned customers within… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …personal development. Are you ready to maximize your potential with us? The Position The Associate Director will be the lead who is responsible for ensuring that ... Reports to the Sr. Director , Patient Support Solution Quality/Safety Associate Director . Interacts with colleagues within Patient Support Programs, Patient… more
- Genmab (Plainsboro, NJ)
- …implemented, and utilized at a pace never seen before. Join Genmab as an Associate Director , Solution Architecture and Engineering, R&D Digital Products as part ... IT R&D Digital Products Team. This role will be reporting to the Director of Engineering and Solution Architecture, R&D Digital Products. The Solution Architect will… more
- Genmab (Plainsboro, NJ)
- …in a timely mannerExecute operational strategies related to drug supply, regulatory submissions, and recruitmentBudget and PlanningAssist in the initial development ... leading clinical projectsExperience managing/guiding internal (cross-functional) and external (CRO, regulatory authorities) teamsSome experience with operational management and budget… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Corporate Accounting guidelines in accordance with IFRS regulations. Relationships Reports to the Associate Director of Accounting at Novo Nordisk Inc. As part ... year-end financials (balance sheet, income statement reviews and supplementary information ) to the SVP of Finance & Operations and...Provide monthly status reports on closing process to the Associate Director of Accounting, the Senior … more
- Merck (North Wales, PA)
- …/Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible for the review and approval of all US ... promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional practices are consistent… more
- Taiho Oncology (Princeton, NJ)
- Associate Director , Regulatory Affairs Strategy Princeton, NJ, USA Req #415 Wednesday, November 27, 2024 Looking for a chance to make a meaningful difference ... from regulatory agencies. + Write procedures. + Effectively present information to internal and external clients. + Apply mathematical concepts to such… more
- J&J Family of Companies (Spring House, PA)
- We are recruiting for an Associate Director to join the Regulatory Medical Writing team to support the Oncology therapeutic area. The position may be located ... This role will report directly to the Hematologic Malignancies Disease Area Head, Regulatory Medical Writing, Oncology. + Is the primary point of contact for MW… more
- Bristol Myers Squibb (Princeton, NJ)
- …. **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of biomarkers, companion ... pharmaceutical products across therapeutic areas + Responsible for understanding the regulatory landscape, assessing regulatory risk, and developing global… more
- Humana (Trenton, NJ)
- …part of our caring community and help us put health first** The Associate Director , Compliance ensures compliance with governmental requirements. The ... Associate Director , Compliance requires a solid understanding of how organization...role will require the effective identification of operational and regulatory risk and the resolution of complex technical and… more
- Bristol Myers Squibb (Princeton, NJ)
- …work and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director , Statistical Programming, provides functional expertise and ... of technical solutions for integrating, analyzing and reporting clinical data. Associate Director drives the development and implementation of innovative… more
- Penn Medicine (Hamilton, NJ)
- …Our employees shape our future each day. Are you living your life's work? Associate Medical Director Summary: + To provide high quality comprehensive clinical ... participates in the psychiatric on-call system. In collaboration with the Medical Director for the Outpatient Site, provides clinical and administrative oversight of… 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 ... development (MIDD) to routinely enable efficient drug discovery/development and/or regulatory decisions. The Pharmacometrics group within QP2 brings an...Associate Director will work with scientists within… more
- J&J Family of Companies (Raritan, NJ)
- Johnson & Johnson Innovative Medicine is recruiting for Associate Director , RA Submissions. The position can be located on-site/hybrid in the US (Titusville, NJ; ... product development process. + Proficiency in the use of Regulatory Information Systems, and submission planning and publishing tools + Proficiency… more
- Penn Medicine (Plainsboro, NJ)
- …that the department is run according to institutional policies and any applicable regulatory requirements. The Associate Director assists and supports the ... Are you living your life's work? Summary: + The Associate Director is responsible for overseeing staff,...and implements departmental policies and procedures to comply with regulatory requirements as well as pharmacy best practices. +… more
- Bristol Myers Squibb (Princeton, NJ)
- …their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director of Specialty Laboratory Quality is responsible for ... laboratory audit program, with an emphasis on risk-based management, regulatory strategy development (ie, fit-for-purpose), and monitoring the regulatory… more
