- Merck & Co. (Upper Gwynedd, PA)
- …medicines. Our Oncology medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire cycle ... and the further study of marketed compounds. In executing these duties, the Senior Director may: Supervise the activities of Clinical Scientists in the execution… more
- Merck & Co. (Boston, MA)
- …Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will manage the entire ... execution, monitoring, analysis, regulatory reporting, and publication.Specifically, the Senior Director May Be Responsible For: Evaluating pre- clinical and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …trained, following process and SOPs. The Director will ensure the Senior Director , Clinical Operations (Asset Lead) is fully informed of the overall ... and aligned strategy.Responsibilities:Operational Strategy and Oversight:Align with the Senior Director , Global Clinical Operations on plans for successful… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Global Clinical Supply (GCS) organization is accountable for managing the 'end-to-end' integrated clinical supply chain across our company ... Research Laboratories portfolio of clinical trials.- GCS is accountable for the planning, sourcing, labeling, packaging and delivery of clinical supplies to … more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new...The Position The position serves as the lead of Clinical Data Science & Evidence (CDSE) operations. In their… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Director , Clinical Pharmacology actively contributes to multi-disciplinary teams by providing innovative ... interpreting study data and effectively communicating findings to a broad audience. The Director , Clinical Pharmacology will be relied upon to act independently,… more
- Eisai, Inc (Nutley, NJ)
- …#LI-CCEisai Salary Transparency Language:The base salary range for the Senior Director , Clinical Quality Assurance - Remote-Based is from :236,900-310,900Under ... 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
- Eisai, Inc (Baltimore, MD)
- …and make a difference. If this is your profile, we want to hear from you. Director , Clinical Quality Assurance The Director , Clinical Quality Assurance ... activities. Eisai Salary Transparency Language:The base salary range for the Director , Clinical Quality Assurance is from :195,000-256,000Under current… 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 ... novel insights and complement internal pipeline.Monitor emerging biology and basic & clinical research within metabolic diseases & obesity, and more broadly across… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Job Summary: The Sr. Director , Clinical Safety MD, will lead the development and implementation of ... key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new...you ready to make a difference? The Position The Director , Real World Science leads the evidence strategy and… more
- Merck & Co. (Rahway, NJ)
- …Description: Our Research and Development Division's microbiology team is seeking a Director for the Rahway NJ GMP microbiology operations.- The primary objective of ... oversee GMP environmental monitoring and microbiological release of pipeline products.- The director will provide guidance, lead activities, and strengthen a team of… more
- Merck & Co. (Rahway, NJ)
- …pipeline programs using fed-batch and continuous manufacturing platforms. The Director , Biologics Process Development (BPD) within the Biologics Process Research ... high yields along with superior product quality and allow speedy progression for clinical studies and commercial launch. The candidate will be a member of the… more
- Merck & Co. (Rahway, NJ)
- … clinical implementation and advancing digital pathology within our company's clinical therapeutic pipeline.The Principal Scientist ( Director ) will have the ... Molecular Biomarkers is responsible for translating preclinical molecular biomarkers to clinical development across all therapeutic areas and all phases of … more
- Merck & Co. (Rahway, NJ)
- …external partnerships that grow our portfolio in meaningful ways. - The Director , Business Development & Licensing - Enabling Technologies Search and Evaluation, ... of partner scientific areas in conjunction with functional area and clinical development leadership.- For example, the Enabling Technologies team supports areas… more
- Merck & Co. (Rahway, NJ)
- …enables gain of critical internal experience during scale-up of clinical supplies manufacturing, demonstration of new manufacturing technology/processes, training ... pilot plant. The Facility Lead position reports to the Director of Operations/Head of SSO Pilot Plant and the...members to ensure the quality and safe delivery of clinical supplies, the scientific rigor of the processes, and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Job Summary: The Director of Data Management (DM) Reporting provides leadership in Data Management ... and external stakeholders to oversee the development and delivery of clinical data programming, reporting, data visualizations, external data acquisition and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new...you ready to make a difference? The Position The Director Medical Review oversees a team of Medical Reviewers… more
- Merck & Co. (North Wales, PA)
- …responsible for the formulation and execution of automation strategy in Global Clinical Trial Operations and all the support activities within their functional area. ... This includes working with stakeholders across Global Clinical Trial Operations (GCTO)and other relevant teams, driving the strategy from ideation to value… more
- Merck & Co. (Rahway, NJ)
- …team is to carry out analytical GMP activities partnering across the network to enable clinical supplies. In this role, the Director of the Raw Materials and ... product release testing across the entirety of our non-sterile and sterile clinical portfolio. The Director is responsible for ensuring cGMP compliance… more
