- Merck & Co. (Rahway, NJ)
- …group includes strategy development, strategy execution and value realization, enterprise strategic planning, risk management, and strategic venture investments ... is large, diverse and evolving rapidly. Within ESO, we provide deep strategic partnership in developing, assessing and shaping our strategy at the portfolio,… more
- Merck & Co. (Rahway, NJ)
- …development in the (bio)pharmaceutical and/or medical device industries to set tactical and strategic direction on programs they lead to ensure high quality ... Principal Scientist - Device Technical and Engineering Lead (Associate Director Equivalent) Our company's Device Product & Process Development (DPPD)… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWe're looking for a Director of Quality Assurance to lead quality across the full value chain for a late-stage ophthalmic program . In this role, ... and Supply Chain teams-coaching, facilitating, and removing obstacles so the program can thrive.Bring energy, knowledge, innovation to carry out the following:Own… more
- Merck & Co. (Rahway, NJ)
- …initiatives.Partnering with discovery and clinical colleagues to shape research programs .Analyzing select competitor activities through strategic assessments, ... are currently seeking a Cardiovascular & Respiratory Competitive Intelligence Director specializing in PAH, COPD, and other cardiopulmonary diseases. This… more
- Merck & Co. (Rahway, NJ)
- …to support the R&D efforts related to the Insider Risk/Trade Secret (IR/TS) program through advanced data analysis and strategic collaboration. This role plays ... of the group lead, the successful candidate will manage day-to-day program activities, foster strong stakeholder partnerships, and champion innovative solutions that… more
- Merck & Co. (Rahway, NJ)
- …Development and Technology Organization. Thisposition is responsible for providing strategic program leadership, technical expertise, and project management ... Job DescriptionThe Associate Director - Device Tech Transfer is a leadership role...business goals, and quality and regulatory compliance.Essential Duties and Responsibilities: Program Leadership and Technical Project Management:Provide program … more
- Merck & Co. (Rahway, NJ)
- …design verification strategies for assigned drug-device combination product program (s) for successful clinical introduction(s) and commercial market(s) ... regulatory submissions (INDs, IMPDs, NDAs, BLAs, etc.) for combination product programs under your leadership.Lead/ Support clinical supplies production with respect… more
- Merck & Co. (Rahway, NJ)
- …Management, Data Quality Assessments, Documentation Review, Employee Training Programs , FDA Regulations, IT Coordination, IT Operation, Pharmacovigilance, Policy ... Implementation, Regulatory Compliance, Regulatory Labeling, Regulatory Operations, Regulatory Submissions, Strategic Thinking {+ 1 more}Preferred Skills: Current Employees apply… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …of the Technical Operations team based in Raritan, NJ. Role OverviewThe Associate Director of Engineering is a strategic and operational leader responsible for ... Johnson, to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel). Our strategic partnership is designed to combine the strengths and expertise of… more
- Merck & Co. (Rahway, NJ)
- …and pipeline products to produce safe, effective, innovative medicine.The Clinical Director is responsible for protocol development and medical/ scientific oversight ... trial results.In addition to responsibilities associated with clinical research, the Clinical Director at this level will be expected to lead a Product Development… more
- LiveRamp (New York, NY)
- …benefits package offers medical, dental, vision, life and disability, an employee assistance program , voluntary benefits as well as perks programs for your ... the forefront of rapidly evolving compliance and privacy requirements.** The Sales Director is an individual contributor role who creates, identifies, and closes… more
- Formation Bio (New York, NY)
- …in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to ... bring new treatments to patients faster and more efficiently.About the PositionThe Director of Clinical Project Management will provide overall leadership and … more
- Formation Bio (New York, NY)
- …in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to ... faster and more efficiently.What We Are Looking ForWe are seeking a Director of Technical and Transaction Accounting with deep biotech industry experience and… more
- Formation Bio (New York, NY)
- …in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to ... new treatments to patients faster and more efficiently.About the PositionThe Senior Director , Regulatory Affairs lead is responsible for developing and directing the… more
- Formation Bio (New York, NY)
- …in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to ... innovations during development, collaborating with BD to position IP assets for maximum strategic value, and collaborating with our AI/tech teams as we build out our… more
- Formation Bio (New York, NY)
- …in-licenses drugs from pharma companies, research organizations, and biotechs to develop programs past clinical proof of concept and beyond, ultimately helping to ... development, for clinical studies. As part of this responsibility you will provide strategic input to and monitor the execution of clinical studies as a project… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …(below VP) and early career hiring strategies and designs policies, practices, and programs in accordance with our People philosophy.Acts as a Global Business Unit ... Talent Acquisition Lead responsible for bridging strategic workforce planning and operational execution for assigned global business unit and/or function(s).Lead a… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Publications, Medical Slides, and other related projects). Collaborate with Medical Director responsible for Communication Strategy and Medical Program ... research areas centered around rare diseases and immune disorders. Summary Director , Global Medical Affairs Oncology Publications works with Cross Functional Team… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …all Medical Affairs programs . This role involves deputizing for the Sr. Director , representing the Quality organization at senior levels. The Director plays ... including interventional studies, non-interventional studies, Compassionate Use or Managed Access Programs .Collaborate with the Sr Director , Medical Affairs QA… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Director Global Medical Affairs Oncology (GMA), ADC, under the direction of the ... Senior Director , GMA Oncology ADC (Global Medical Affairs team lead...lead for compound), is responsible for assisting with defining compound/ program medical strategies and for leading select medical affairs… more
