- Eisai, Inc (Nutley, NJ)
- …of the Quality management system. This role is responsible for Good Clinical Practice (GCP) and for assuring the compliance of projects, products and programs ... and assess long-term resource, technology, and skill needs for respective program (s) within clinical quality area.Anticipate immediate and long-term risks… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to best support each program . This position will require line management responsibility of Directors, Associate Directors, Clinical Study Managers, who are ... other research areas centered around rare diseases and immune disorders. SummaryThe Senior Director of Clinical Operations will manage clinical operations… more
- Merck & Co. (North Wales, PA)
- …Skills:Adaptability, Adaptability, Budget Development, Business Acumen, Business Development, Clinical Supply Chain Management , Clinical ... Job DescriptionGlobal Project and Alliance Management (GPAM) sits in the Research & Development...business development activities independently, regardless of complexity, phase or program type, and is based on direct experience and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryThe Associate Director Global Medical Affairs Oncology (GMA), under the direction of the ... Senior Director / Director , GMA Oncology (Global Medical Affairs team...lead for compound), is responsible for assisting with defining compound/ program medical strategies and for leading select medical affairs… more
- Merck & Co. (Rahway, NJ)
- …be a valued co-strategist on asset cross-functional meetings: Franchise Teams, Clinical , Value-Evidence, Risk Management , and Commercial Product Development ... Job DescriptionThe Global Senior Director of Medical Affairs (GDMA) for Melanoma coordinates...assigned Product Development (Sub-) Teams. Contributes to Life Cycle Management decisions. In addition, the leads the Medical Affairs… more
- Merck & Co. (Sacramento, CA)
- Job DescriptionThe Regional Medical Scientific Director (RMSD) is a credentialed (ie, PhD, PharmD, DNP, MD) therapeutic and disease expert who engages in ... expertise.This position will support our Company's Gastrointestinal (GI) Immunology program .Location: The position covers the following exemplar states: WA, OR,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …teams.Ensure consistent and proactive representation of Quality at all stages of the program management process.May Interact with management at all levels ... assigned programs or continuous improvement projects, championing and implementing study/ program -specific quality plans for proactive quality management .Collaborate… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as other research areas centered around rare diseases and immune disorders. SummaryThe Director US Medical Affairs (USMA) Oncology, under the direction of the Senior ... Director , USMA Oncology (US Medical Affairs team lead for...lead for compound), is responsible for assisting with defining compound/ program medical strategies and for leading select medical affairs… more
- Merck & Co. (Rahway, NJ)
- …therapeutic areas and modalities to drive portfolio impact from discovery through life-cycle management . The team is externally visible and continues to be at the ... leader to drive pipeline impact and lead a talented group of pharmacometricians.This director will be part of a leadership team responsible for applying traditional… more
- Taiho Oncology (Philadelphia, PA)
- …and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources ... team at Taiho Oncology Inc. As a Regional Business Director (RBD), you will play a crucial role in...experience in oncology sales. Minimum 3+ years' oncology sales management experience. Working knowledge of geographic condition / customer… more
- Merck & Co. (Rahway, NJ)
- …recommendation of repurchase strategies, dealer selection and full execution management .Manage relationships with repurchase dealers and monitor program ... Job DescriptionThe Executive Director , Global Capital Markets leads critical financial functions...Development, Capital Management , Capital Markets, Cash Flow Management , Clinical Judgment, Communication, Debt Management… more
- Merck & Co. (North Wales, PA)
- Job DescriptionThe Executive Director , Scientific Affairs (EDSA) maximizes meaningful bi-directional scientific exchange with the worldwide clinical and academic ... outcomes for patients. The EDSA leads a large investigator-initiated studies program in partnership with late-stage development teams in Medical Affairs while… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Executive Director (ED) for US Medical Affairs (USMA) understands Our Company's enterprise level strategies and leads cross-functionally with the ... including tactical execution by the field Regional Medical Scientific Director (RMSD) teams and is accountable for ensuring field...sets the strategic direction for the Therapeutic Area (TA) program , and oversees the execution of the field medical… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Medical Director will provide medical leadership for medical affairs strategy, planning and supportive tactics ... for assigned therapeutic area. Under the direction of the Senior Medical Director , this role will be responsible for working with key stakeholders to develop and… more
- Merck & Co. (Rahway, NJ)
- …Mammalian Cell Culture, Mentoring Staff, Negotiation, People Leadership, Pharmaceutical Management , Pharmaceutical Process Development, Process Scale Up, Program ... pipeline programs using fed-batch and continuous manufacturing platforms. The Director , Biologics Process Development (BPD) within the Biologics Process Research… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Medical Director will provide medical leadership for medical affairs strategy, planning and supportive tactics ... plan. Provide strategic development, planning, implementation and oversight of Phase IV clinical trial programs and RWE studies within the Medical Affairs department… more
- Insmed Incorporated (San Diego, CA)
- …with Clinical Development, Clinical Operations, CMC, QA/QC, Nonclinical, Program Management , and external consultants to align regulatory results and ... Women™, Best Workplaces for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Director , Regulatory Affairs will serve as the regulatory leader on… more
- Formation Bio (New York, NY)
- …sciences (biotech, pharma, or consulting) with at least 3+ years in people management Deep expertise in AI/ML for predicting biological/ clinical outcomes with ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
- Merck & Co. (Rahway, NJ)
- …Scientist is a senior scientific role tasked with working closely with the group Director to define group strategy and to lead a team of scientists in solving ... transfer of assays. Plan assay optimization and documentation to meet program deadlines.Authoring and reviewing internal technical reports, sections of regulatory… more
- Merck & Co. (Rahway, NJ)
- …Scientist is a senior scientific role tasked with working closely with the group Director to define group strategy and to lead a team of scientists in solving ... develop talent through good mentoring skills. Experience with matrix management and peer to peer coaching - - -...of release, characterization, and stability assays for testing of clinical trial material and in support of product and… more
