- Daiichi Sankyo, Inc. (Bernards, NJ)
- …supporting early clinical safety for our Rare Disease/Specialty Medicine portfolio. SummaryThe Director , Clinical Safety , will be a product safety lead ... safety team, and be responsible for overall product safety strategy or specific areas of safety surveillance and risk management, and provide safety … more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or ... span all phases of clinical development (pre-clinical to post-licensure). The Senior Director will manage the entire cycle of late-stage clinical development and… more
- Merck & Co. (Rahway, NJ)
- …Rahway, New Jersey.The Sterile Process Engineer role at the Associate Director level will leverage the individual's leadership, technical, and communication ... change management.Familiarity with United States and European Union GMP and Safety compliance regulations.Ability to convert new drug product attributes and process… more
- Merck & Co. (Rahway, NJ)
- …enable and accelerate process and product development and manufacturing and ensure safety and quality of our products. The successful candidate will be accountable ... cross-functional development teams to enable pipeline decisions. -The Executive Director , Biologics Analytical Research and Development (B-AR&D) is responsible for… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as R shiny apps for data surveillance, visualization, modeling and simulations, and safety signal detection. Lead the development and validations of R package and/or ... R capabilities and implementations. Collaborate with CSPV to enable/effectively support safety signaling detections and across compounds safety reviews (ie,… more
- Merck & Co. (Rahway, NJ)
- …to transform drug delivery and manufacturing technology to positively impact patients.The Director of Oral Formulation Sciences will lead a team of scientists and ... Critically, the individual will drive a culture of perpetual adherence to safety and compliance standards. A successful candidate should have extensive drug product… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …oversight groups for case processing activities and reports to the Director of PV Case Management.Responsibilities:ICSR Processing: Oversees QC activities, supports ... PV; required10 or more years of experience within Drug Safety /Pharmacovigilance experience, including both investigational and marketed products; preferredExtensive… more
- Merck & Co. (Rahway, NJ)
- …that enable and accelerate process and product development and manufacturing and ensure safety and quality of our products. -The Director , Biologics Analytical ... of candidates from the discovery interface, through first product registration.- -The Director will be responsible for a team of approximately 10-15 scientists and… more
- Merck & Co. (Rahway, NJ)
- …Operations, Drug Delivery Systems and Devices within our Manufacturing Division (Associate Director ).-This role serves as a Virtual Plant Manager - responsible for ... to deliver Pharmaceutical, Biologic, and Vaccine Products. Our team works with a " Safety First, Quality Always" mindset.-As the primary point of contact for all… more
- Merck & Co. (Rahway, NJ)
- …support business objectives, with focus on Process Design and Process Safety for Small Molecule High Potency/Containment Projects. Develop project scope, front-end ... Participate in development and review of engineering guidelines, standards, safety /environmental policies, and change requests. Define intent in Front-End Loading,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. Summary: The Senior Director , Head of RBQM (Risk Based Quality Monitoring) sets the vision and ... risk factors with and for other technical departments (eg, Clinical, Medical, Safety , Data Management, Statistics). This position requires skills in working in a… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …improvement of Clinical Development processes. Job Description:Execute an overarching safety program tailored for AEs from end-to-end: understanding predisposing ... and beyond in post approval setting.Responsible for the execution of key safety initiatives aimed at preventing, mitigating, and addressing critical safety … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. JOB SUMMARYThe Senior Director , Head Medical affairs Quality Assurance in Global RD/PV QA is accountable ... TeamsGOMA and Specialty MA Management teamsData Management/ Biostats Clinical Safety and PharmacovigilanceR&DVendors/ CROs/ third partiesHEOR/ RWEEpidemiology Legal and… more
- Tris Pharma (Monmouth Junction, NJ)
- …in our Monmouth Junction, NJ facility for an experienced, hands-on SR. Director / Director , Procurement. Title and salary commensurate with experience. The ... Director / Senior Director , Procurement is responsible for...(FDA), Drug Enforcement Administration (DEA), and Occupational Health and Safety Administration (OSHA) regulations, as well as all applicable… more
- Eisai, Inc (Nutley, NJ)
- …If this is your profile, we want to hear from you. The Director , HCP Marketing, Alzheimer's Disease will lead several core marketing, strategy, and lifecycle ... digital experience across HCPs, Consumers, and SOC to drive adherence and safety as patients start therapy. Partner with Market Access, Eisai Patient Support,… more
- Eisai, Inc (Nutley, NJ)
- …Management, Clinical Safety Data Review and Clinical team. The Assoc. Director of Clinical Programming will oversee the Data Review programming and JReview ... this is your profile, we want to hear from you. The Associate Director , Clinical Programming must have expertise in addressing technical challenges in the… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionOur Clinical Development teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new ... applying rigorous scientific and ethical standards.-The Distinguished Scientist (Executive Director ) and Product Development Team (PDT) lead, Oncology Global… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director (Principal Scientist) has primary responsibility for the planning and directing of clinical research activities involving new or marketed ... 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 & Co. (Rahway, NJ)
- Job DescriptionThe Director (Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed ... span all phases of clinical development (pre-clinical to post-licensure). The Director will manage the entire cycle of clinical development, including study… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …future capabilities. We're responsible for regulating accounting, upholding workplace safety , managing our supply chain and sampling, supporting technological and ... data innovation, maintaining our facilities and assuring the integrity and completeness of all business transactions. At Novo Nordisk, you will have the opportunity to build a life-changing career in a global business environment. We encourage our employees to… more
