- 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 ... The Position The position serves as the lead of Clinical Data Science & Evidence (CDSE) operations. In their...planning: Set up the annual strategy to action (S2A) process of making sure the departmental strategy is aligned… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …We are seeking a strategic leader for the role of GxP Patient Safety, Compliance & Vendor Oversight within our Clinical , Medical & Regulatory (CMR) organization. ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...position combines the critical functions of patient safety training, compliance curriculum management, and vendor oversight to ensure adherence… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …for patient support field teams. This role will oversee program operations, compliance , vendor contracts and relationship management. AD will drive collaboration and ... functions, including Commercial Strategy and Marketing, Insights & Analytics, privacy, compliance and legal. Relationships The position reports to the Director,… 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 ... and quality tasks performed by suppliers and business partners to ensure compliance with SDEA requirements. Relationships This position reports to the Associate… more
- Merck & Co. (Rahway, NJ)
- …development process & connectivity between functions supporting pipeline (ie clinical development, CMC, supply chain, & human health), and balancing needs of ... Leadership, Data Analysis, Drug Development, Logistics, Multiple Therapeutic Areas, Process Optimization, Publications Management, Regulatory Compliance , Risk… more
- Merck & Co. (Rahway, NJ)
- … Practice (GCP) studies, and occasionally Good Laboratory Practice (GLP) studies. The Associate Principal Scientist is the primary clinical study team leader and ... Clinical Trials Operations, Computer Science, Design, Detail-Oriented, Ethical Compliance , Ethical Standards, GLP Regulations, Good Clinical Practice (GCP),… more
- Merck & Co. (Rahway, NJ)
- …the way we approach serious diseases. --The Senior Director will report to an Associate Vice President in the Oncology Clinical Research Group. Under the ... Senior Director has primary responsibility for the planning and directing of clinical research activities involving new or marketed Oncology medicines. Our Oncology… more
- Merck & Co. (Rahway, NJ)
- …Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the ... area. Our company's Atherosclerosis & Metabolism medicines span all phases of clinical development (pre- clinical to post-licensure). The Senior Director will… more
- Merck & Co. (Rahway, NJ)
- …field and relevant experienceRequired Experience and Skills:-- -A deep understanding of the clinical trial process : You can speak the language of protocols, ... Job DescriptionWe are seeking an Associate Principal Scientist to contribute to a pivotal...stewarding these data, you will empower our scientists and clinical teams to make faster, data-driven decisions that propel… more
- Merck & Co. (Rahway, NJ)
- …and operational experience to lead and support facility operations, process development activities, compliance investigations/change management, authoring of ... Compliance , Immunochemistry, Industrial Hygiene, Innovation, Inventory Management, Management Process , Manufacturing Quality Control, People Management, Pharmaceutical Biology, Pharmaceutical… more
- Merck & Co. (Rahway, NJ)
- …strategies for innovative combination products?Join our company's Device Product & Process Development (DPPD) Team, which focuses on the design, development, and ... areas and routes of administration, including inhalation, implantation, and injection.The Associate Principal Scientist will lead the definition and execution of… more
- Merck & Co. (Rahway, NJ)
- …be responsible to establish and lead cross-functional teams through the sourcing process and to provide strategy oversight for regional and/or local components of ... of the business in the category during the course of Sourcing Management Process . Typical Activities : Meetings with stakeholders to discuss Sourcing Management … more
- Merck & Co. (Rahway, NJ)
- …and ADaM standardsDemonstrated success in the assurance of deliverable quality and process compliance .Strategic thinking - ability to turn strategy into tactical ... License:NoHazardous Material(s):n/aRequired Skills:-Preferred Skills:Algorithms, Algorithms, Applied Mathematics, Biostatistics, Business Process Improvements, Business Strategies, Clinical Development, … 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 ... performance against project goals and milestones to monitor and ensure compliance with Daiichi Sankyo Clinical Study Oversight Plan (CSOP).Responsibilities-… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …and Goals: Assist CSPV Leadership in developing PV goals, continued compliance , and strategy for process improvement initiatives. Qualifications: Successful ... and aggregate reporting for DSI products, both investigational and marketed. Maintains compliance with Global PV regulations for individual case safety and periodic… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …a global role that will cover signal activity across all DS regions. The Associate Director of the Signal Management Center of Excellence (CoE) will lead the daily ... across the global safety organization. The incumbent will ensure regulatory compliance , promote best practices, foster a culture of continuous improvement in… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Operations Associate as part of the Technical Operations team based in Raritan, NJ. ... is responsible for quality and maintaining the highest standards in compliance within company policies, procedures, and all applicable regulations.Schedule: Sun-Wed,… more
- Teleflex (New York, NY)
- Associate Sales Representative, Trauma and Emergency Medicine - NYC **Date:** Oct 24, 2025 **Location:** New York City, NY, US **Company:** Teleflex **Expected ... This entry-level medical device sales role is designed to support the sales process across Teleflex's trauma and emergency medicine portfolios. The Associate … more
- Memorial Sloan-Kettering Cancer Center (New York, NY)
- …Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of ... deep learning approaches as well as application of developed technology to clinical cancer cases, in collaboration with MSK radiologists. Futher information of the… more
- Memorial Sloan-Kettering Cancer Center (New York, NY)
- …Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of ... around the globe. Exciting Job Opportunity at MSK: **Payroll Associate - Time and Attendance** Are you a resilient...all while maintaining a high level of accuracy and compliance with federal and state labor laws. + Provide… more
