- Merck & Co. (Rahway, NJ)
- …motivated and experienced Anatomic Pathologist (MD) for the role of Principal Scientist ( Director ) to join our innovative team. This position will play a crucial ... pathology within our company's clinical therapeutic pipeline.The Principal Scientist ( Director ) will have the following responsibilities: Engage in providing… more
- Merck & Co. (Rahway, NJ)
- …increasing overall operational effectiveness.We are seeking a dynamic and experienced Associate Director of Outside Counsel and Vendor Management to join our Legal ... report directly to the Chief of Staff to the General Counsel & Executive Director , Legal Operations, Innovation & Technology and will be based in Rahway, NJ.- This… more
- Merck & Co. (Rahway, NJ)
- …software . - Familiarity with Good Manufacturing Practices (GMP) requirements, quality procedures , and Standard Operating Procedure (SOP) execution. - - - - ... #eligibleforERP GCSCareer25 #VETJOBS #MSJR #GCSCareer Current Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that… more
- Merck & Co. (New York, NY)
- …are seeking a Growth and Improvement minded Oncology Regional Medical Scientific Director that can help drive our Strategic Operating Priorities. Invent-- Pursue the ... must reside in the territory.Strategic Summary The Oncology Regional Medical Scientific Director is a credentialed (ie, PhD, PharmD, DNP, MD) oncology expert who… more
- Eisai, Inc (New York, NY)
- …and monitor individual and overall compliance with Eisai policies and procedures and external regulatory requirements (eg, FDAMA 114).Provide operational oversight ... engagement, and future growth of the team. Qualifications: Regional Business Director - ADBachelor's degree (Master's preferred) and 10+ years of relevant… more
- Formation Bio (New York, NY)
- …bring new treatments to patients faster and more efficiently.About the PositionThe Director of Medical Writing will be responsible for developing and implementing ... with applicable principles of Good Clinical Practice (GCP), Standard Operating Procedures (SOPs), and regulatory guidelines. About You Bachelor of Science Degree,… more
- Formation Bio (New York, NY)
- …Author, review and approve analytical technical documents and standard operating procedures (SOPs) in collaboration with Quality colleagues to assure compliance with ... specification justification reports, retest and shelf-life memos, standard operating procedures and other technical documents following regulatory requirements. Experience… more
- Eisai, Inc (Nutley, NJ)
- …a difference. If this is your profile, we want to hear from you. Director , Clinical Quality Assurance The Director , Clinical Quality Assurance position is ... compliance of projects, products and programs with Eisai's Standard Operating Procedures (SOPs), Policies, and all applicable worldwide regulations and guidelines… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Sr. Director , Data Quality and Integrity (Global R&D & PV QA) ensures high ... process improvements. Collaborating with the Global QMS eCompliance team, the director oversees QA plans, promotes data governance, and engages stakeholders to… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionDescription The Associate Director position's core responsibilities are to oversee our Company's compliance related to customs country of origin. In ... and the oversight of our company's Free Trade Agreement usage. The Associate Director position's key responsibilities are around these programs; as well as handling… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …analyzes issues and opportunities which are within established policies and procedures and engages stakeholders to gain alignment and endorsement of solutions.Builds ... Strategy.Identifies, defines and analyzes course (s) of action within established procedures and policies and engages stakeholders to gain alignment and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary: The Senior Director , Head of RBQM (Risk Based Quality Monitoring) sets the vision and ... in project execution and deliverables. Oversees or initiates RBQM operating procedures and standards; monitors and enforces compliance of standard procedures… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …diagnostics and devices.Experience of drug development and drug regulatory procedures .Understanding of strategic and tactical role and deliverables of Global ... Regulatory Strategy in the Drug and Device Development and Commercialization process.Experience with developing and documenting regulatory strategies in coordination with clinical plans and marketing objectives. Experience with communicating the regulatory… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryThe Associate Director FP&A position is an integral part of the finance team supporting ... on reasons for any variances and implications on business performance. Works with Director of FPA to streamline and improve reporting to offer management insights to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary: The Associate Director , Laboratory Data Management is accountable for the end-to-end delivery of ... both in-house and outsourced studies.- Accountable for laboratory data management procedures and authorships of specification documents to ensure standardization is… more
- Merck & Co. (Rahway, NJ)
- …DescriptionReporting to the Customs & International Trade (CIT) Tariff Classification Associate Director , the Senior Specialist will work closely with our Research & ... as required and contributes to developing and maintaining related standards and procedures .- This position assists with the development and upgrade of classification… more
- Merck & Co. (Rahway, NJ)
- …Reporting to the Customs & International Trade (CIT) Valuation Associate Director , the Senior Specialist position's core responsibilities are to oversee our ... to the development and maintenance of customs valuation standards and procedures and to design and upgrade customs valuation related training materials.Provide… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Strategy:Align with the Head of Clinical Development Operations or Senior Director , Clinical Operations on plans for successful implementation of studies. ... their responsibility.Design, update and implement appropriate innovative and best-in-class procedures and SOP's related to clinical study oversight and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …/ Vendor Oversight: Review CRO/vendor proposal and budget. Establishes procedures through regular interaction, setting expectation on deliverables and timelines ... to guide CRO biostatistician and statistical programmers on complex studies. Ensures deliverables are accurate and delivered according to the timelines.Global Health Authority Interaction / Negotiation: Contributes to documents submitted to Health Authorities… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …projects. Play a key leadership role in support of all processes and procedures around change management. This role requires comfort and independence in leading ... complex initiatives of high dollar value from inception through to implementation and ability to handle global projects through established interactions with Japan and Europe as required.Responsibilities- Lead the Global Finance and Procurement Capability… more
