- Bristol Myers Squibb (Princeton, NJ)
- …Requirements + Advanced Degree in related field (MS, Ph.D. or PharmD) + For Associate Director with Ph.D. approximately 5+ years of experience with demonstrated ... scientists, project leadership, early and late clinical development teams and commercial colleagues to provide input on clinical pharmacology profiling, dose… more
- AbbVie (North Chicago, IL)
- …functionality, enriching the user experience for all employees. About the Role As Associate Director of Digital Accessibility, you will spearhead efforts to ... leadership well-informed of progress and impact. This position reports to the Director of Digital Experience & Innovation at AbbVie's global headquarters in Lake… more
- Rhythm Pharmaceuticals (Boston, MA)
- …overcome barriers, together. Opportunity Overview Rhythm Pharmaceuticals is seeking an Associate Director , Non-Clinical Research with demonstrable experience and ... strategy . This role will report into the Sr. Director , Non-Clinical Development. Responsibilities and Duties + Support/lead Rhythm's non-clinical programs,… more
- Bristol Myers Squibb (Seattle, WA)
- …Read more: careers.bms.com/working-with-us . We are seeking a highly motivated and experienced Associate Director of Cell Therapy Process Development to lead and ... This role will be pivotal in shaping our cell therapy strategy , partnering cross-functionally with manufacturing, quality, regulatory, and external collaborators. A… more
- Amneal Pharmaceuticals (Bridgewater, NJ)
- Description: The Associate Director , Corporate Development will serve the role of sourcing, evaluation, execution and, most importantly, alliance management of ... in or out, creating regular check-ins with various constituents across Finance, Legal, Commercial , R&D and of course BD. This role will focus on key out-licensing… more
- Glenmark Pharmaceuticals Inc., USA (Elmwood Park, NJ)
- Associate Director , Regulatory Affairs Department: Regulatory Affairs Location: Elmwood Park, NJ START YOUR APPLICATION ... Supplements to post-approval work. Form 2252 for Annual Reports. + Provide support/RA strategy needed to achieve timely approvals with the Agency. + Update the… more
- Takeda Pharmaceuticals (Boston, MA)
- …and pharmacovigilance perspective of regulated post-authorization activities in the commercial business units and affiliates. + Contributes to and implements ... the engagement strategy among R&D, Business Units and affiliates and Quality...place for the transition of R&D pipeline to the commercial space. + Drives a fit-for-use global Quality framework… more
- S&P Global (New York, NY)
- …**Grade Level (for internal use):** 12 **S&P Dow Jones Indices** **The Role:** Associate Director , Fixed Income Product Management **The Firm** S&P Global is ... world-wide, we are is responsible for the development, production, strategy and commercialization of our bond index index suite...lines; help identify new product opportunities to help drive commercial success + Be viewed as a key subject… more
- AbbVie (Barceloneta, PR)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The ME&C Associate Director is a global program management expert responsible ... + Exposure to quality systems, design controls, product labeling, regulatory submission strategy /preparations and product launch/ commercial supply are a plus. +… more
- Turner & Townsend (Indianapolis, IN)
- …the world. **Job Description** **Turner & Townsend** are looking for an experienced ** Associate Director Cost Manager and/or Quantity Surveyor** to lead cost ... first point of contact for reporting on the overall commercial status of a project. + Drive Turner &...+ Undertake Staff Performance reviews. + Set a clear strategy and ambition for the team. + Identify, coach… more