- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across the full our ... Research & Development Division portfolio of clinical trial s .- GCS is accountable for the...for the planning, sourcing, labeling, packaging and delivery of clinical supplies to clinical sites globally. The… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. ... documents under guidance of higher level. Reviews and oversee completion of clinical trial protocols. Provides medical and/or scientific direction to Clinical … more
- Aequor (Thousand Oaks, CA)
- 100% onsite Thousand oaks The ideal candidate for the Clinical Supply Chain Senior Associate role will have prior experience in clinical supply chain or a ... a background in downstream logistics will be given priority. Posting Title: Clinical Supply Chain Senior Associate - Vendor ManagementJob Description: Under… more
- Genmab (Plainsboro, NJ)
- …best, and authentic is essential to fulfilling our purpose.Overview The Global Clinical Trial Manager, Team Manager (GCTM-TM) is responsible for line management of ... approximately 12 direct reports, including Clinical Trial Managers (CTMs) and Clinical Trial Associates (CTAs), for larger programs or trials. This role provides… more
- Merck & Co. (Rahway, NJ)
- …execution of clinical studies.--Will report and work collaboratively with the- Associate Vice President to promote the development strategy of the company on the ... commercialization, regulatory affairs, statistics, medical affairs and manufacturing to manage clinical development projects; and assist the Associate Vice… more
- Aequor (South San Francisco, CA)
- …hours aligned to CA (preferably someone located in PST) Not looking for a clinical trials mangers or clinical researchers. This is an operational focused project ... ask to submit neutral examples) Specific Job Requirements: The Clinical Biomarker and Diagnostics (CBD) Operations Lead plans and...OR Bachelor's degree and 5 years of experience OR Associate 's degree and 10 years of experience OR High… more
- Merck & Co. (Rahway, NJ)
- …and compliant medical products, practices and solutions to the world.-The Associate Principal Scientist Regulatory Affairs supports products in the General Medicine ... and conducting research on regulatory guidances or competitive intelligence.- The Associate Principal Scientist will have responsibility for driving results for… more
- Merck & Co. (Rahway, NJ)
- …Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical ... organization and has oversight over drug development aspects related to clinical pharmacology and pharmacometrics of oncology drugs from post-PCC to registration.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Job Summary: The incumbent will be responsible for ensuring the delivery execution of clinical studies in one or more geographic regions, in adherence to Good ... Clinical Practices (GCPs), appropriate Standard Operating Procedures (SOPs), Food...primarily a tactical study delivery role, reporting into an Associate Director (or above) responsible for Operational Study Strategy.… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Job Summary: The Manager, Clinical Data Repository Administration is a member of the Biostatistics and Data ... maintenance of standard hierarchy structures and user access controls for all clinical studies. This position may have direct reports and/or dedicated external… more
- Merck & Co. (Rahway, NJ)
- …of decision-making at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate ... PK/PD models, exposure response (ER) models, model-based meta analysis (MBMA), clinical trial simulations (CTS) and disease progression modeling into programs and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …MA and Plainsboro, NJ. We support programs from early research through late-stage clinical development. We are building for the future, creating a distinct R&D ... you ready to make a difference? The Position The Associate Global Medical Director will serve as a pivotal...and a commitment to excellence in all aspects of clinical practice and scientific exchange. Vision Statement US East… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Vice President (AVP) will be responsible for leading the Translational Medicine (TMed) Cardiovascular & Respiratory Therapeutic Area and ... strategy, bridging the continuum from Discovery Research through Late-Stage Clinical Development.- The AVP provides strategic oversight for the early clinical … more
- Merck & Co. (Rahway, NJ)
- …Description - - Our Company Research Labs IT team partners with the Clinical Trial Operations teams within the Research & Development division to create, develop, ... and enhance innovative solutions to complex problem s . We are seeking a highly motivated and passionate P roduct Manager for Trial and Site Management P roduct L ine to own the product vision, strategy, and roadmap of the assigned product .- The Product… more
- Merck & Co. (North Wales, PA)
- …programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and ... tables, listings, figures), the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support.The… more
- Aequor (Thousand Oaks, CA)
- …attribute knowledge to advance products and ensure success through pivotal clinical phases to marketing authorization application. Key Responsibilities: - Select ... suitable methodology and techniques to develop and validate analytical methods for testing synthetic small molecule and/or synthetic oligonucleotides for drug substances and/or drug products. - Hands-on experience in sample preparation and analysis of… more
- Merck & Co. (Lower Gwynedd, PA)
- …area of Regulated Bioanalytical Exploratory Development. Our team is exploring clinical and preclinical immune responses to vaccination leveraging modern automation, ... bioanalytical vaccine immunogenicity assays to support regulated preclinical and clinical vaccine development. The individual will be responsible to contribute… more
- Genmab (Plainsboro, NJ)
- …our best, and authentic is essential to fulfilling our purpose.The Role The Associate Director of US Medical Affairs Hematology Strategy will report to the Director, ... market through collaboration with US Commercialization, Global Medical Affairs, Clinical Development, Regulatory, and other cross functional teams.We have a… more
- Merck & Co. (Rahway, NJ)
- …company's biologics pipeline. We work closely with colleagues in Discovery, Pre- clinical and Early Development to rapidly develop manufacturing processes for diverse ... biotherapeutics, and efficiently manufacture material to supply clinical trials. We are also responsible for commercial process development and the development and… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- Legend Biotech is seeking a Warehouse Operations Associate as part of the Warehouse & Logistics team based in Raritan, NJ. Role OverviewThe Warehouse Operations ... Associate will be part of the Technical Operations Supply...production of a personalized cell therapy to support both clinical and commercial requirements in a sterile cGMP environment.… more
