- Merck & Co. (North Wales, PA)
- …in the Research & Division organization of our company.- Position Description/Summary: The GPAM Associate Director , Project Manager, is a core member of Early ... Job DescriptionThe drug development Project Manager is part of ...& Development pipeline and realize its full potential. The Associate Director is expected to provide project… more
- Merck & Co. (North Wales, PA)
- …and external stakeholders with processes that ensure compliance with local and global PV regulations.Ensure that PV activities are supported by robust procedures ... reserves the right to require COVID-19 vaccinations for positions, such as in Global Employee Health, where the Company determines in its discretion that the nature… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Associate Vice President (AVP) has primary responsibility for the planning and directing clinical research activities involving new or marketed ... drugs for oncology indications. The Associate Vice President will manage and oversee the entire cycle of clinical development, including study design, initiation,… more
- Merck & Co. (North Wales, PA)
- …and manufacturing to manage clinical development projects; andAssist the Executive Director / Associate Vice President in ensuring that appropriate corporate ... an environment of mutual respect, encouragement and teamwork. As part of our global team, you'll have the opportunity to collaborate with talented and dedicated… more
- Merck & Co. (North Wales, PA)
- …to develop strategies and tactics to attain profitable market access for a macrocyclic peptide drug . -The Director will be a subject matter expert on US health ... Job DescriptionThe Director , US Pharma Payer Marketing Atherosclerosis leads a...developing access strategies and tactics for a macrocyclic peptide drug , our Company's investigational novel treatment for adults with… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- … Global Safety Lead(s), Global Safety Lead(s) and Global Safety Scientist(s)/ Associate within Safety Surveillance. Essential Functions Innovation and ... or a life sciences/pharmacy nursing degree with 15+ years' experience in global safety surveillance and/or clinical/ drug development Excellent verbal and written… more
- Tris Pharma (Monmouth Junction, NJ)
- …have an immediate opening in our Monmouth Junction, NJ facility for an Associate Director , Alliance Management.Tris Pharma has a long track record of ... spanning many departments across all stages of the product lifecycle. The Associate Director , Alliance Management will be accountable for managing alliances… more
- Bristol Myers Squibb (Princeton, NJ)
- …Lead , this role partners with senior leaders across Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory, IT, Audit, Finance and HR to build and ... compliance program into the Worldwide Medical, R&D and Global Drug Development Organizations . In this...their decisions. + Under the direction of the Senior Director , US and Above Market Medical and Market Access… more
- Bristol Myers Squibb (Princeton, NJ)
- …a BMS Global Program Team (GPT) in early and/or late development. The Associate Director PM will provide content expertise to the timing, costs, and ... partner and operational lead for development and lifecycle management programs, the Associate Director GPM works to ensure that cross-functional teams operate… more
- Merck (North Wales, PA)
- …the Research & Division organization of our company. **Position Description/Summary:** The GPAM Associate Director , Project Manager, is a core member of Early ... drug development Project Manager is part of Global Project and Alliance Management (GPAM) which sits in...& Development pipeline and realize its full potential. The Associate Director is expected to provide project… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning - GI2 ... high performance teams and mentoring colleagues. + Significant experience in global drug development regulations, regulatory submissions, lifecycle management,… more
- Takeda Pharmaceuticals (Trenton, NJ)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... of labeling content and strategy of multiple assigned products in various stages of drug development, which may include one high complexity product and updates to or… more
- Bristol Myers Squibb (Princeton, NJ)
- …lives. Read more: careers.bms.com/working-with-us . **Position Responsibilities** + Develop global and/or US regulatory strategy for Oncology products in development ... direction and provide leadership for all regulatory interactions with FDA/ global regulatory authorities + Lead regulatory dossier submissions to...and guidelines as they apply to US FDA for drug development and approval. + Expert understanding of … more
- Merck (North Wales, PA)
- …internal and external stakeholders with processes that ensure compliance with local and global PV regulations. + Ensure that PV activities are supported by robust ... reserves the right to require COVID-19 vaccinations for positions, such as in Global Employee Health, where the Company determines in its discretion that the nature… more
- Bristol Myers Squibb (Princeton, NJ)
- …address external questions regarding drug products. The CMC Regulatory Associate Director , Biologics is responsible for content development, compilation, ... Sciences (GRS) and Global Product and Supply (GPS). The GRS-CMC Associate Director , Biologics will assess Manufacturing Change Controls for global… more
- Ascendis Pharma (Princeton, NJ)
- …and the Americas and supporting global needs as required. The RA Associate Director , Labeling will be overall responsible for ensuring compliance with US ... Ascendis Pharma is a dynamic, fast-growing global biopharmaceutical company with locations in Denmark, Europe,...grow and develop their skills. The Regulatory Affairs (RA) Associate Director , Labeling will be responsible for… more
- J&J Family of Companies (Titusville, NJ)
- Associate Director , Temperature Strategy & Execution - 2406177829W **Description** Johnson & Johnson Innovative Medicine Research & Development (JJIM R&D), part ... of the Johnson & Johnson Family of Companies, is recruiting for an Associate Director , Temperature Strategy & Execution within Clinical Supply Chain (CSC). The… more
- Merck (Upper Gwynedd, PA)
- …and Pharmacometrics -** **Immune/Oncology** team in the role of Associate Director . The team is part of the Global Clinical Development organization ... Directors are emerging leaders in the field of quantitative drug development, with a developing understanding of the strategic...effective communication skills. As a subject matter expert, the Associate Director within the Group will work… more
- Bristol Myers Squibb (Princeton, NJ)
- …at work and in their personal lives. Read more: careers.bms.com/working-with-us . Associate Director , TA (Therapeutic Area) Analysis Standards Leader is ... across the TA, aligning cross-functionally and driving end to end standards. Associate Director , TA Analysis Standards Leader, independently leads improvement… more
- Merck (West Point, PA)
- **Job Description** **Position Description:** ** Associate Director , Quality Systems & Compliance** Our Quality Assurance group ensures every single material ... on time, every time, across the globe. **Position Responsibilities:** + The Associate Director is responsible for performing comprehensive and detailed GMP… more
