- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and regulatory compliance.Keep abreast of evolving regulations and industry standards concerning data integrity, representing the company in industry forums or ... around rare diseases and immune disorders. SummaryThe Sr. Director, Data Quality and Integrity (Global R&D & PV QA)...stakeholders (RD, PV and MA) to drive timelines and report on key deliverables related to quality and compliance.… more
- Merck & Co. (Rahway, NJ)
- …that enable new organizational capabilities.Decision Science is seated within the Data Science and Scientific Informatics (DSSI) team of Research and Development ... and design solutions. Our solution process involves mathematical modeling of data and processes implemented through efficient and modular computational tools to… more
- Merck & Co. (Rahway, NJ)
- …functional potency assay technologies, such as cell line engineering to build reporter gene assays, cytotoxicity assays.- Expertise in binding assays such as ... immunoassays. Strong knowledge and statistical skills for interpretation of potency data in context of broader process and product development.- Working knowledge of… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …that prioritizes the needs of patients and healthcare providers while aligning with company goals. Utilize data and consumer insights to continually assess and ... for patients and healthcare providers. We are a group of innovative, data driven, cross-functional leaders that focusing on driving the strategy and execution… more
- Merck & Co. (Rahway, NJ)
- …This role requires excellent analytical, negotiation and communication skills.This role will report directly to the Chief of Staff to the General Counsel & ... in Rahway, NJ.- This position will work closely with and oversee the company 's eBilling Administrator. Law Firm and Legal Vendor Management: Ensure excellence in… more
- Merck & Co. (Rahway, NJ)
- …and/or PhD whose primary function is to design, coordinate, monitor, and report clinical laboratory and field studies that will support the regulatory approval ... Ambition - Respect - Inclusion.Design and organization of paper and Electronic Data Capture (EDC) clinical studies that meet scientific and regulatory requirements… more
- Merck & Co. (Boston, MA)
- …(RaDS) value team in R&D IT brings together product management, engineering, and data science expertise. We enable data , technology and services that accelerate ... to join the RaDS Product organization. The position will report to the-Lead of the Disease Biology and PharmTox...partner closely with key business stakeholders, the product, engineering, data science and other IT teams, to leverage advanced… more
- Merck & Co. (Rahway, NJ)
- … manager packages. Strong understanding of Enterprise Process Management to troubleshoot report /input templates (in cases of master data or other validations) ... provide operations solutions reviewing and analyzing system and passive data governance reports to ensure high quality data...submitted by search firms to any employee at our company without a valid written search agreement in place… more
- Novo Nordisk Inc. (West Lebanon, IN)
- …Primary responsibilities include validation protocol execution (IQ, OQ, PQ & PV), data analysis and final report preparation for utilities, equipment and ... in the pharmaceutical or biotechnology industry Experience preparing protocols, executing data analysis, and report writing Experience preparing protocols,… more
- Merck & Co. (Rahway, NJ)
- …partners, designs studies, authors study protocols, develops measurement questionnaires, case report forms, data analysis plans, final study reports, scientific ... and vendor/partner management and to ensure study conduct is aligned with company Policies and SOPs and world-wide regulations and standards, including Good… more
- Merck & Co. (Rahway, NJ)
- …negotiating costs, executing contracts and ongoing contract management. This role will report to the Associate Director, Clinical Trial Central Labs to support high ... such as Legal, Privacy, Compliance, etc.Supplier Performance Management - to monitor, report , manage, and continuously improve supplier performance as part of a… more
- Merck & Co. (North Wales, PA)
- …and Research Decision Sciences), a distinguished department within our company 's renowned Research and Development division, quantitative scientists, in partnership ... the entire product lifecycle. - Primary Activities : Effective analysis and report programming development and validation utilizing global and TA standards and… more
- Merck & Co. (North Wales, PA)
- …through the entire product lifecycle. Primary Activities :Effective analysis and report programming development and validation utilizing global and TA standards and ... in developing analysis and reporting deliverables for R&D projects ( data , analyses, tables, graphics, listings)Strong project management skills; leadership at… more
- Genmab (NJ)
- …and study-related materialsDevelop and maintain the study TMF PlanClinical Study Report (CSR) Management:Support filing appendices of Clinical Study Report ... with the unknown and be innovativeYou have experience working in a fast-growing, dynamic company (or a strong desire to)You work hard and are not afraid to have… more
- Genmab (NJ)
- …Advances this effort through the coordination and development of data -driven early indication and program assessments, study-level feasibility assessments, robust ... delivery for all stages of global feasibility. Ensure standardization in use of data , tools and processes to inform risk-benefit decision making at TA, program and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …strategy, focusing on every touchpoint that impacts our customers. We leverage data and insights to inform our decision-making processes, ensuring that our ... and MASH programs, ensuring market/product/organizational readiness. Relationships This position will report to the VP of Future Portfolio, Pipeline Strategy and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product development, CMR is involved. The ... any required documents to regulatory agencies. Supervise designated personnel. Relationships Report to the Director Regulatory Affairs. Develop and maintain positive… more
- Eisai, Inc (Mckinney, TX)
- …caregivers is Eisai's human health care (hhc) mission. We're a growing pharmaceutical company that is breaking through in neurology and oncology, with a strong ... with a primary responsibility of engaging in the exchange of scientific data and other medical and/or scientific information with external customers (healthcare… more
- Taiho Oncology (FL)
- …Department with a primary responsibility to engage in the exchange of scientific data , education of health care practitioners on Taiho products and relevant disease ... and medical information between Key Opinion Leaders (KOLs)/investigators and the company 's Medical Affairs and development groups. Establish, foster, cultivate and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …strategy, focusing on every touchpoint that impacts our customers. We leverage data and insights to inform our decision-making processes, ensuring that our ... for setting and communicating clear individualized role expectations for each report based on position, skills, talents, and objectives. Ensure that reporting… more
