- 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)
- Job DescriptionThe Executive Director (Distinguished Scientist) has primary responsibility for the planning and directing of clinical research activities involving ... of the Atherosclerosis & Metabolism therapeutic area. The Executive Director will manage and oversee the entire cycle of...the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications,… more
- Merck & Co. (Rahway, NJ)
- …with a passion for biologics? We're looking for a dynamic and visionary- Director , Drug Substance Leader-to drive innovation and excellence across our Biologics ... diverse internal and external teams to deliver as One Team Champion compliance, safety , and a culture of diversity, equity, and inclusion Foster transparency and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director / Principal Scientist, Regulatory Affairs Liaison , is responsible for the development and implementation of worldwide regulatory strategy ... single point-of-contact for products within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS.Key functions:Reports to Senior Principal… more
- Merck & Co. (Rahway, NJ)
- …and status updates to project sponsors and management.Champion compliance and safety ; promote a culture of diversity, inclusion, and equity.Minimum Education ... Requirements and Experience: - Bachelor's degree in Chemical Engineering, Bioengineering, Biological Engineering, or a related field with fourteen (14) years of combination of experience including team management, technical expertise in cell culture, and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAbout the Role:-As a Technical Lead, you will report into Director , Chemical Technical Operations, External Manufacturing API Technology, and play a ... performance. Maintain a strong focus on compliance and Environmental Health and Safety (EHS) to drive supply excellence. Serve as the primary technical contact… 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)
- …enhance data monitoring capabilities, and drive excellence in safety , compliance, supply, and productivity.Global Impact:Collaborate with colleagues across ... diverse teams to achieve program goals as One Team. Champion compliance and safety ; promote a culture of diversity, inclusion, and equity. Experience and aptitude to… 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
- Formation Bio (New York, NY)
- …bring new treatments to patients faster and more efficiently.About the PositionThe Director of Medical Writing will be responsible for developing and implementing ... briefing packages, regulatory filings); and pharmacovigilance documents (eg, annual reports/developmental safety update reports) by serving as the document author or… 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Executive Director , Head of Center of Excellence (CoE), Global Medical Safety ... various regions, offering guidance and support to each product safety team in critical areas such as individual case...such as individual case medical review, risk management, aggregate safety reports, and translational medical safety . This… 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)
- …areas centered around rare diseases and immune disorders. Summary: The Associate Director , Laboratory Data Management is accountable for the end-to-end delivery of ... data in Daiichi Sankyo R&D collaborating with clinical and medical teams, clinical safety and pharmacovigilance, CROs and other vendors to ensure high quality of… 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)
- …centered around rare diseases and immune disorders. Job Summary: The Senior Director sits within Global Oncology Clinical Development, an organization dedicated to ... assessment of protocol deviationsDiscusses medical eligibility questions and answers safety questions (dose modifications, discontinuations, and management of adverse… 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
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …develop programming submission strategy, perform integrated analysis of efficacy and safety , generate submission data package, create TLFs to support submission QAs, ... perform ad-hoc and exploratory analysis requested by clinical team, and support agency response or potential Advisory Committee Meeting- Develop DSI programming standard template on datasets and TFLs to improve efficiency and quality. Responsibilities include:… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …environment. This pivotal position will report directly to the Senior Director of Operations.Key Responsibilities Champion and lead the employee engagement program ... with company policies and standards while promoting a culture of safety and engagement.Requirements Bachelor's degree in Human Resources, Marketing, or… more
- Allied Universal (New York, NY)
- …perks, and more. **Allied Universal is currently looking to hire a Fire Life Safety Director for a Corporate Building Midtown, Manhattan** + Position is: Full ... + Pay Rate: $28.00 / hour The primary mission of the **Fire life Safety Director ** is to protect life and property through the implementation of the building's… more
