- Merck & Co. (Rahway, NJ)
- …& Technology (DD&T) organization designs, develops, and commercializes novel biologic/ drug / vaccine - device enabled combination products to achieve safe and ... set direction for the device development strategy for multiple drug -device combination product development programs ranging from concept generation/selection,… more
- Merck & Co. (Rahway, NJ)
- …high-volume clinical and commercial assembly equipment and processes for medical devices/ drug delivery systems. Reporting to the Director responsible for this area, ... equipment and processes for clinical and commercial manufacture of drug -device combination products.Hands on troubleshooting in a manufacturing environment with… more
- Merck & Co. (Rahway, NJ)
- …Analysis (RCA), Stakeholder Engagement, Stakeholder Relationship Management, Standards Compliance, Strategic Thinking, Technical Transfer-Preferred Skills:API ... ManufacturingJob Posting End Date:08/8/2025 *A job posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID:R358817 more
- Merck & Co. (North Wales, PA)
- …Clinical Trial Compliance, Clinical Trial Management, Communication, Data Analysis, Dermatology, Drug Development, Ethical Standards , ICH GCP Guidelines, Life ... and presentation skillsEducation/ExperienceBachelor's Degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical field experience OR… more
- Merck & Co. (Rahway, NJ)
- …Trial Management, Clinical Trials Analysis, Communication, Critical Thinking, Data Analysis, Drug Development, Ethical Standards , ICH GCP Guidelines, Life ... - Education/Experience Bachelor's Degree +5 years of pharmaceutical , clinical drug development, project management , and/or medical field experience OR Master… more
- Merck & Co. (North Wales, PA)
- …Trial Management, Communication, Communication Management, Cross-Functional Teamwork, Data Analysis, Drug Development, Ethical Standards , ICH GCP Guidelines, ... Outlook, etc.)Education/Experience: Bachelor's Degree +5 years of pharmaceutical, clinical drug development, project management, and/or medical field experience/ Master's… more
- Merck & Co. (North Wales, PA)
- …Trial Documentation, Clinical Trial Planning, Consultative Approach, Cross-Cultural Awareness, Drug Development, Ethical Standards , Innovation, New Technology ... organization; widely recognized within the organization as an expert in drug development.Demonstrated ability to understand and manage, with appropriate support, the… more
- Merck & Co. (Rahway, NJ)
- …In summary, our team enables the translation of preclinical candidates into non-oral drug products.We are seeking a highly motivated candidate for the position of ... Principal Scientist (R5) focused on developing parenteral drug products across a range of modalities (small molecule,...a large capital project team, knowledgeable of the Sterile Standards and equipment design standards , and understanding… more
- Formation Bio (New York, NY)
- …is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more ... technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses… more
- Formation Bio (New York, NY)
- …is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more ... technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses… more
- Genmab (NJ)
- …scientific and technical progress within the field of biostatistics in drug development and advise of new methodologies that may support innovation ... related work is performed in accordance with Genmab SOP/processes and standards and ICH-GCPCTT member:Participate and represent BiostatisticsReview and provide input… more
- Merck & Co. (Rahway, NJ)
- …global human health.Responsibilities: The Senior Statistical Programmer, Submission Data Standards Quality Management (SDS QM), provides oversight and quality ... data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects. Accountability predominantly includes… more
- Merck & Co. (Rahway, NJ)
- …by integrating state-of-the-art technology and applying rigorous scientific and ethical standards .The Senior Director has primary responsibility for the planning and ... of generating early clinical development plan and Investigational New Drug applications;Developing clinical development strategies for investigational or marketed… more
- Formation Bio (New York, NY)
- …is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more ... technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses… more
- Formation Bio (New York, NY)
- …is a tech and AI driven pharma company differentiated by radically more efficient drug development. Advancements in AI and drug discovery are creating more ... technology platforms, processes, and capabilities to accelerate all aspects of drug development and clinical trials. Formation Bio partners, acquires, or in-licenses… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally ... (Dx) Partner to communicate key RA updates from the drug side, as needed. Provide RA specific inputs into...robust development of assay, participate in HA interaction for drug -related CDx topics/questions, and attend device company HA meetings… more
- Merck & Co. (Rahway, NJ)
- …Our Team as an Associate Principal Scientist/Associate Director in Biologics Drug Substance Commercialization!Are you ready to make a significant impact in ... forefront of innovation in the-Manufacturing Division, specifically within the-Biologics Drug Substance Commercialization (BDSC) team. Our Downstream Purification-department is… more
- Merck & Co. (North Wales, PA)
- …statistical programming activities for multiple and/or late stage drug /vaccine clinical development projects. -Accountability predominantly includes the development ... and report programming development and validation utilizing global and TA standards and following departmental SOPs and good programming practices.Maintain and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally ... rare diseases and immune disorders. Job Summary: This position oversees ICSR Standards activities, projects, and procedures. This level interacts within global CSPV… more
- Merck & Co. (Rahway, NJ)
- …Development & Technology (DD&T) Team designs, develops, and commercializes novel biologic/ drug /vaccine - device enabled combination products to achieve safe and ... patents, and professional activities.Stay current with relevant regulations, technologies, standards , and effectively share this knowledge with others.Qualifications MINIMUM… more
