- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Associate Director, Clinical Programming must have expertise in addressing technical challenges ... will be responsible for implementing new technological solutions for end users.The Associate Director, Clinical Programming manages and oversees JReview and SAS… more
- Merck & Co. (Rahway, NJ)
- …and program cost estimates requested by Product Development Teams.-Responsible for authoring clinical supply documentation in support of labeling and packaging ... chain documentation to support critical CMC activities.-- Support the collection of clinical supply chain...critical CMC activities.-- Support the collection of clinical supply chain metrics and/or participate in critical non-pipeline… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …knowledge-based coordination, authoring, and management of Dose Preparation Instructions in support of clinical studies being conducted globally by Daiichi ... The candidate will collaborate globally with Formulation and Analytical Scientists, Clinical Operations, Regulatory Affairs CMC, and Clinical Development to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … clinical studies, under the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence to the protocol, Good ... Conference on Harmonization (ICH) guidelines. Key focus is on providing clinical trial management support to study teams and tracking CRO and other vendor… more
- Merck & Co. (Rahway, NJ)
- …ongoing contract management. This role will report to the Associate Director, Clinical Trial Central Labs to support high quality sourcing initiatives and ... Job Description Position Description: The selected candidate will provide procurement support for Clinical Development Sourcing and Procurement (CDSP) in C… more
- Aequor (South San Francisco, CA)
- …of time in the office (49% Homeoffice allowed) Job title Global Clinical Materials Manager Department PTDS-Global Competency Center Production Enablement Reports to ... Head Global Clinical Materials Management Locations SSF1. Duties and Responsibilities, Interfaces...with KPIs and taking applicable actions for continuous improvements Support of warehouse in goods receipt questions Perform virtual… more
- Merck & Co. (Boston, MA)
- … trials for investigational or marketed Atherosclerosis drugsAnalyzing and summarizing the clinical findings from studies to support decisions regarding safety ... Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the… more
- Merck & Co. (Boston, MA)
- …and execution for investigational or marketed medicinesAnalyzing and summarizing the clinical findings from studies to support decisions regarding safety ... experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects, and assist the Associate Vice President… more
- Aequor (Aliquippa, PA)
- …buying experience as this role will have buying responsibilities Accountabilities Support business processes related to NA-TO Back Office and process improvements ... Execute GDP/ GMP and business processes in the scope of ATO Support Office with minimum supervision Manage outbound/ inbound distribution schedule with appropriate… more
- Merck & Co. (South San Francisco, CA)
- …Data, AI and Genome Sciences (DAGS)-Department is recruiting-an Associate Director, Computational Biology-in-Cardiometabolic Drug-Discovery-Data Sciences. We are ... to leverage our Company's investments in human genetics and other-multimodal data to support drug discovery in the cardiometabolic disease space. The Associate … more
- Genmab (NJ)
- …like a fit? Then we would love to have you join us!The RoleThe Associate Director, External Data Quality Management, is a strategic leadership role within ... Clinical Data Management. This individual is accountable for driving...for inspection readiness, regulatory compliance, and successful data submissions.The Associate Director will lead cross-functional collaboration, provide oversight of… more
- Eisai, Inc (Exton, PA)
- …Functions 1. Oversee the operations of the Upstream and Downstream Operations groups to support the supply of DS/ADI for pre- clinical and phase I to phase ... your profile, we want to hear from you. The Associate Director of Biologics Operations Upstream and Downstream is...Downstream production staff in the operation of equipment to support preclinical and phase I to III clinical… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionContainer Closure Integrity Testing Lead, Associate Principal Scientist, Analytical Research & Development The Analytical Research and Development ... group has an opening for an Associate Principal Scientist based in Rahway, NJ. Join us...CCIT, as we establish CCIT testing capabilities for our clinical portfolio in various product images (vial, syringe, medical… more
- Aequor (Thousand Oaks, CA)
- …compliance with clinical regulatory requirements, partner with key stakeholders to support inspection readiness for various clinical programs and clinical ... Fully remote MCS Supply Chain Sr Associate Ideal candidate: Experience is document management. Very...orientation and detail oriented Description: Reports to (Sr.) Mgr Clinical Supply Chain. Candidates will, under limited supervision and… more
- Merck & Co. (North Wales, PA)
- …is responsible for the design and maintenance of statistical datasets that support multiple stakeholder groups which include clinical development, outcomes ... statistical programming activities for multiple and/or late stage drug/vaccine clinical development projects. -Accountability predominantly includes the development and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Strategy: - Establishes company-wide laboratory data management strategies and processes in support of clinical development objectives.- Accountable for lab data ... areas centered around rare diseases and immune disorders. Summary: The Associate Director, Laboratory Data Management is accountable for the end-to-end delivery… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary:The Associate Director, Oncology Value & Market Dynamics Training Manager is responsible ... access for patients across our portfolio of products. The Associate Director will develop, in partnership with other key...marketplace. The role will lead the training efforts and support the needs of a variety of DSI teams… more
- Aequor (Thousand Oaks, CA)
- We are seeking an enthusiastic, collaborative Associate Scientist to join our In Vivo Pharmacology Team in the Oncology Therapeutic Area in Thousand Oaks, CA. In ... on laboratory rodents such as handling, dosing (via multiple routes), clinical health assessments, and biologic sample collection. Additional tasks will include… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …diseases and immune disorders. Summary: Responsibility for regulatory strategy to support the development of biomarkers, companion diagnostic tests and other devices ... of a CDx study/IVDR performance evaluation study integration of an assay into clinical testing (before testing) and once data is ready for CDx submission (after… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- … support submission QAs, perform ad-hoc and exploratory analysis requested by clinical team, and support agency response or potential Advisory Committee ... trials analysis preferred- Advanced understanding of statistical concepts in support of analyses and reporting of clinical ...in support of analyses and reporting of clinical trials preferred- Knowledge of all phases of drug… more
