- Taiho Oncology (Princeton, NJ)
- …marketed and/or investigational products assigned, including review and analysis of safety data from clinical trials and from post-marketing sources, providing ... expertise to assigned project teams, the identification and investigation of safety signals, management of benefit-risk profile for assigned products and review… more
- AristaCare (Cherry Hill, NJ)
- …+ Complete room rounds to observe and evaluate resident's physical/emotional state and safety . Has knowledge of resident's condition at all times. Ensure rooms are ... + Provide direct patient care when needed. + Keeps Director of Nursing informed of status of patient and...meetings of the facility (ie, Infection Control, Policy Advisory, Pharmaceutical , Quality Assessment, etc.) as required. + Assist in… more
- Hovione (East Windsor, NJ)
- …as an integrated Contract Development and Manufacturing Company dedicated to helping Pharmaceutical Customers bring new and off-patent drugs to market. Our people ... Agreements) and Quality Agreements for allocated accounts in close collaboration with the Director of the area. * To lead the negotiation of complex contracts,… more
- Mitsubishi Chemical Group (Jersey City, NJ)
- …company - one of Japan's most respected - is a research-driven pharmaceutical company that has tirelessly pursued medical breakthroughs with global reach. MTPC ... development, distribution, importation, export, and vendor management in cooperation with Director of Commercial Supply Chain. This incumbent will drive supply chain… more
- Merck (Rahway, NJ)
- **Job Description** The Director (Principal Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or ... span all phases of clinical development (pre-clinical to post-licensure). The Director will manage the entire cycle of clinical development, including study… more
- Merck (Rahway, NJ)
- …Description** Our Clinical and Pharmacovigilance teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new ... technology and applying rigorous scientific and ethical standards. The Senior Director has primary responsibility for the planning and directing clinical research… more
- Merck (Rahway, NJ)
- …closely with team members and partner groups including formulators, engineers, Quality, Safety , and Facilities management to drive overall success and performance of ... consistent with all applicable internal and external regulations for quality (GMP), safety , etc. + Attention to Detail: Maintain meticulous records of formulation… more
- Merck (Rahway, NJ)
- **Job Description** The Senior Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new ... and respiratory medicines. With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development, including study design,… more
- ThermoFisher Scientific (Bridgewater, NJ)
- …unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo ... drug development, laboratory and lifecycle services to customers across pharmaceutical , biotechnology, medical device, academic and government entities. By… more
- Reckitt (Parsippany, NJ)
- …as deemed appropriate. + Coordination of resolution of any quality, compliance and safety issues affecting products in market + In conjunction with the Quality ... Director for NA, responsible for developing and deploying the...of work experience in manufacturing and or distribution of pharmaceutical products, medical devices or food industry in a… more