- Merck & Co. (North Wales, PA)
- Job Description Role Summary: The Global Senior Director Medical Affairs (GDMA) is a subject matter expert in their area of responsibility (eg, defined tumor, ... the World (ROW). -The GDMA may also be appointed as aV&I Lead for their disease/asset area, which includes additional organizationally aligned responsibilities.- The… more
- Eisai, Inc (Nutley, NJ)
- …mgmt. activities. #LI-CCEisai Salary Transparency Language:The base salary range for the Senior Director , Clinical Quality Assurance - Remote-Based is ... If this is your profile, we want to hear from you. The Clinical Quality Assurance Professional (QAP) position is responsible for design, delivery and execution… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …well as other research areas centered around rare diseases and immune disorders. SummaryThe Senior Director of Clinical Operations will manage clinical ... operational and overall delivery and tactical execution of the clinical studies. The senior director ...of the Study Management Group Heads and/or Vice President, Clinical Development Operations.Contribute to and/or lead in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …scientific engagement and communication- Serves as Global Medical Affairs Team (GMAT) Lead , to gain strategic and planning alignment across the matrix team ... as a member of the various cross-functional forums including, Publications Planning, Clinical and Safety sub-teams, and Global Product Team to inform clinical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Job Summary: The Sr. Director , Clinical Safety MD, will lead the development and ... key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Director of Human Factors (HF) will provide visionary leadership and strategic direction for the HF function within our company. This ... of HF principles to enhance patient safety and product usability. The Senior Director will champion enterprise-wide HF strategy, foster cross-functional… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …primary responsibilities of this position are to guide the strategy and to lead the implementation of companion diagnostics (CDx) in support of multiple projects ... drug registration or for any project with CDPs containing multiple registrational clinical trials and are extensively exploring the predictive nature of potential… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …candidate will set goals and enumerate key scientific questions that will drive clinical development decision-making. In doing so, he or she will align closely with ... plan documents, biomarker statistical analysis plans, and aid in the construction of clinical development plans, clinical protocols, and in the submission of… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for assigned compound under the supervision and leadership of the Executive Director of Medical Research and Strategy, US Oncology Medical Affairs (USOMA). Develops ... in Global Medical Affairs committees as requested. Serves as US Medical Affairs Lead , to gain strategic and planning alignment across the matrix team and the… more
- Merck & Co. (Rahway, NJ)
- …and dedicated colleagues while developing and expanding your career.The Executive Director , Chemistry, Manufacturing & Controls ( CMC) , Pre-approval Pharm will ... industry and FDA connections to our company. They will lead a team of CMC professionals, ensuring rigorous CMC...conjugates (ADCs), and traditional solid-oral small molecules.- The Executive Director will help drive our company's growth into new… more
- Merck & Co. (Rahway, NJ)
- …Small Molecule VCM Product Leader (PL) is the end-to-end (E2E) supply chain lead responsible for developing and executing product supply strategies for one or more ... continuity of supply, and commercial outcomes. The VCM Product Leader will lead the cross-functional Supply Chain Working Group (SCWG) for pipeline products or… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …across all Medical Affairs programs. This role involves deputizing for the Sr. Director , representing the Quality organization at senior levels. The Director ... ensure high data quality, proactively identifying and resolving issues throughout the clinical trial process. Customer Focus / Stakeholder:Engagement Lead the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Affairs Oncology (GMA), under the direction of the Senior Director / Director , GMA Oncology (Global Medical Affairs team lead for compound), is responsible ... medical education and other scientific exchange activities in alignment with the Senior Director , such as scientific symposium and medical congresses, within… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … US Medical Affairs (USMA) Oncology, under the direction of the Senior Director , USMA Oncology (US Medical Affairs team lead for compound), is responsible ... the assigned medical affairs plan activities, in collaboration with Sr. Director .- Leads medical readiness activities for market launches. This includes strategic… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Job Summary: Director , Global QA Strategy &Operations (Global R&D PV QA) is responsible for ... promotion of the 6th Mid-Term Strategy for Global QA, lead the execution of the business plan, and manage...high impact.Ability to effectively interact with and present to senior management at all levels, as well as to… more
- Insmed Incorporated (San Diego, CA)
- …teamsCommunicating regulatory strategies and risk assessments to cross-functional teams and senior leadership, as neededCollaborate with Clinical Development, ... within gene therapy or orphan (rare) diseasesPrior experience serving as the regulatory lead on cross functional teams (CMC, clinical and project teams)Ability… more
- Merck & Co. (South San Francisco, CA)
- Job DescriptionThe Executive Director of Metabolism & Obesity will be responsible for overseeing and facilitating the research in metabolic diseases & obesity and ... innovations that make a difference for patients across the globe.Responsibilities include: Lead and help shape the departmental strategy in metabolic disease research… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …execute daily production schedules.Will have 3-6 direct reports ranging from Associate Director , Senior Manager, and Manager.Oversee the hiring, development, and ... in the treatment of multiple myeloma.Legend Biotech is seeking Director of Operations as part of the Technical Operations...production of a personalized cell therapy to support both clinical and commercial requirements in either a Grade C… more
- Formation Bio (New York, NY)
- …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 ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
- Formation Bio (New York, NY)
- …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 ... processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses drugs from pharma… more
