- Merck & Co. (Upper Gwynedd, PA)
- Job DescriptionThe Executive Director , Global Medical and Scientific Affairs (EDMA) GYN Malignancies is accountable for the development and execution of ... Areas (TA). They lead a team of TA dedicated global and regional directors and associate directors....skills Preferred Experience and Skills: At least 5 years global or US medical affairs or clinical … more
- Merck & Co. (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 ... Job DescriptionThe 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
- Merck & Co. (North Wales, PA)
- …the CMV Pack, a key business driver for the US Pharma Business Unit. The Associate Director , Scientific Strategy Lead for CMV will be responsible for developing ... commercial activities that interface with internal and external stakeholders, including Global Marketing, US Medical Affairs, Outcomes Research and key external… more
- Merck & Co. (North Wales, PA)
- …We are currently recruiting for someone to join our US marketing team as the Associate Director , Product Marketing Owner - HCP for the HIV Franchise.The HCP ... ownership of Brand and HCP Strategy and Execution. This position will report to the Director , US Commercial Leader (USCL) and will be based in the Upper Gwynedd, PA… more
- Merck & Co. (North Wales, PA)
- Job DescriptionPosition Description: Associate Principal Scientist, Outcomes Research Under the guidance of a senior leader, an Associate Principal Scientist has ... Economics, Pharmaceutical Administration, Public Health, Health Policy, Medicine, or Clinical Pharmacy)1-3 years relevant experience following advanced or professional… 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
- Merck (Upper Gwynedd, PA)
- …Pharmacology and Pharmacometrics -** **Immune/Oncology** team in the role of Associate Director . The team is part of the Global Clinical Development ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the Group will work closely with teams of… more
- CSL Behring (King Of Prussia, PA)
- …or Amsterdam office. It is a Hybrid role. You will report to the Director Clinical Portfolio Execution. You will develop the operational strategy for a ... take on additional responsibilities as defined by the (Sr) Director Clinical Portfolio Execution. This role may...the clinical trial process.** **Experience overseeing large global clinical trials (pharmaceutical or CRO).** **Budget… more
- CSL Behring (King Of Prussia, PA)
- …biotherapies used to treat serious and often rare conditions. Could you be our next Associate Director , Clinical System Management? The job is located in the ... CSL Behring is a global biotechnology leader, guided by a promise to...is a hybrid position. You will report to the Director eClinical Operations. **Position Purpose:** You will manage the… 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 ... obtain labeling approval by Labeling Senior Management Cross-functional team ( Global Labeling Oversight Committee - GLOC) driving cross-functional collaboration and… more
- Bristol Myers Squibb (Princeton, NJ)
- …, this role partners with senior leaders across Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory, IT, Audit, Finance and HR to build and ... integrate one global compliance program...+ Conduct risk assessments specific to medical affairs and clinical trial /research activities, utilizing a combination of data… 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 ... strategic direction and provide leadership for all regulatory interactions with FDA/ global regulatory authorities + Lead regulatory dossier submissions to global… more
- Bristol Myers Squibb (Princeton, NJ)
- …relationship with the Contact Center Partners covering US Medical Information, Global Escalations, WW SRD and Variant Content. **Key Responsibilities** 1. Execute ... strategy for US customer engagement: Medical Information, Global Escalations, and Variant Content maintenance, and SRD management in alignment with WW Medical… more
- Merck (Upper Gwynedd, PA)
- **Job Description** The **Senior Clinical Director (Sr. Principal Scientist)** has primary responsibility for the strategic planning and directing clinical ... investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical … more
- Merck (North Wales, PA)
- **Job Description** Under minimal guidance of the Executive Director / Director / Associate Director , Pharmacovigilance (PV) Partner Strategy & Management ... partner and vendor PV agreements and leadership of the Global Clinical Safety & Pharmacovigilance (GCS&PV) implementation...and SMPs. + Maintains, in collaboration with the Executive Director / Director / Associate Director … more
- Merck (Upper Gwynedd, PA)
- **Job Description** The Executive Director , Global Medical and Scientific Affairs (EDMA) GYN Malignancies is accountable for the development and execution of ... Areas (TA). They lead a team of TA dedicated global and regional directors and associate directors....**Preferred Experience and Skills:** + At least 5 years global or US medical affairs or clinical … more
- Bristol Myers Squibb (Princeton, NJ)
- …Sciences (GRS) and Global Product and Supply (GPS). The GRS-CMC Associate Director , Biologics will assess Manufacturing Change Controls for global ... to address external questions regarding drug products. The CMC Regulatory Associate Director , Biologics is responsible for content development, compilation,… more
- Bristol Myers Squibb (Princeton, NJ)
- …centralized monitoring for trials across the BMS Research & Development portfolio. The Associate Director , External Data Acquisition is a leadership role with ... the BMS R&D pipeline. This role reports to the Director , External Data Acquisition within GDM and is a...degree preferred **Experience Requirements** At least 7 years of global clinical trial expertise with a focus… 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
- Pfizer (Collegeville, PA)
- …into country feasibility. **Support study team** + With supervision of medical monitor ( director /Sr director ) provides clinical input to protocol/study team ... and reporting. + Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts with healthcare… more
