- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary The Associate Director , Program Management is a senior position responsible for effectively ... of functions in Daiichi Sankyo (DS). Reporting to the Sr. Director , Enterprise Program Management, this position requires a capable leader with strong technology… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWe are excited to introduce a new opportunity for an experienced Program Manager to lead enterprise-wide data and technology programs for our Animal ... head of the Animal Health Office of the CIO.ResponsibilitiesLead program management activities including identifying obstacles, providing guidance, and overseeing… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …group and high-complexity disease work to support critical strategic choices for the clinical program . The DAST Director will collaborate with the DAST Lead and ... core DAST membership to build out disease-focused resources and capabilities. The individual will be a key contributor to a unified Disease Area Strategy across the Oncology Portfolio and organization, support effective communication and collaboration between… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary: The Associate Director , Commercial Training Lead, Oncology will be accountable to lead the ... the Oncology Franchise and to ultimately develop & implement the Training Program to support all aspects of the commercialized portfolio (product, disease state,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders.Summary: The Associate Director , Regional Marketing Conventions & Field Programs will be responsible for ... more, while ensuring adherence to DS policies and procedures. The Associate Director , Regional Marketing Conventions & Field Programs is responsible for managing the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Initiates contact w/KOL and prepares material for KOL interactions on a program based need; Involvement with in-licensing and acquisitions on individual due ... diligence activitiesQualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation. Education Qualifications (from an accredited college or university)Master's Degree or equivalent preferred… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to CDx project teams for the diagnostic, under the direction of the Global Program Teams (GPT) CDx representative for the therapeutic or under the guidance of the ... CDx portfolio leader, covering all areas from CDx assay development through CDx approval and launch. May act as CDx representative to GPT for early-stage programs.Contributes to CDx Partner evaluation and selection activities and manages multiple Companion… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- Director , Clinical Development Join a Legacy of Innovation 125 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative ... events based upon approved Safety Management Team (SMT) materialsSupports overall program safety reporting (eg, Periodic Safety Update Reports (PSURs), Drug Safety… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …define problem statements and provide efficient solutions. required- Demonstrated project/ program management experience required- Certification in one or more ... SuccessFactors modules including Employee Central, Onboarding, Recruiting, Performance, or Compensation preferred- Hands-on experience implementing a global HRIS solution preferred- Solid influence and negotiation skills. Strong vendor management skills… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... events based upon approved Safety Management Team (SMT) materials- Supports overall program safety reporting (eg, Periodic Safety Update Reports (PSURs), Drug Safety… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... events based upon approved Safety Management Team (SMT) materialsSupports overall program safety reporting (eg, Periodic Safety Update Reports (PSURs), Drug Safety… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …serves as the Clinical Safety Scientist Lead for a large, late-stage program or multiple early-stage programs, in order to proactively perform safety surveillance ... serves as the Clinical Safety Scientist Lead for a large, late-stage program or multiple early-stage programs, in order to proactively perform safety surveillance… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for given commodities/business areas and leading the overall supplier relationship management program for DSI, for DS products and alliances. Cultivates a high ... as the Project Management Owner for DSI's overall Supplier Relationship Management Program (SRM) with Tier 1 suppliers which includes robust comprehensive supplier… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …processes, and on Joint Alliances. Assess and articulate regional interdependencies, program regulatory risks, and opportunities in the development of global ... regulatory strategy and plans, considering therapeutic area strategy, corporate goals, and regional regulatory requirements/precedence.Represent Daiichi Sankyo's regulatory group in internal and external development project meetings. Provide guidance to peers… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Leads broad collaboration with KOLs or major institution, eg NCI.Scientific, Program related: Integrated Study Team (IST) representative: Creates early development ... plan and contributes to overall development Strategy; Develops program biomarker strategy; Achieves endorsement for plan by function and team; Interprets and react… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of Clinical Development processes. Job Description:Execute an overarching safety program tailored for AEs from end-to-end: understanding predisposing non-clinical ... and clinical factors, diagnosis, effective management during clinical trials and beyond in post approval setting.Responsible for the execution of key safety initiatives aimed at preventing, mitigating, and addressing critical safety issues including but not… more
- Merck & Co. (Rahway, NJ)
- Job Description Job Description - Our Cross-Divisional Marketplace Program team is seeking an experienced Technical Product Manager to lead and drive our ... a unique opportunity to shape the future of our Cross-Divisional Marketplace Program by driving the design and implementation of cutting-edge data solutions. -… more
- Merck & Co. (Rahway, NJ)
- …execution of Phase 1-4 clinical studies. Under the direction of the Program Lead, you will collaborate with global, cross-functional team members including clinical ... clinical data/medical protocol deviations in collaboration with the Clinical Director .Builds talent and capabilities of direct/indirect team members through… more
- Merck & Co. (Rahway, NJ)
- …oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team ... portfolio and influence bridging strategies across the portfolio. The Biopharmaceutics Director will work with their direct reports to proactively develop and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director , Business Analyst, within Metrics, Analytics & Performance (MAP) will lead activities related to the development, delivery, & ... and optimize the metrics platform for functional areas and trial/ program teams.-Supports external benchmarking activities to monitor internal performance against… more
