Director, Clinical Research, Obesity Merck & Co IncDirector, Clinical Research, ObesityRahway, NJ$255,800–$402,700 / yearWork closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the team in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. The Director (Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Metabolism section of the Atherosclerosis & Metabolism therapeutic area, with a focus on obesity and obesity-related disorders.
Executive Director, Medical Affairs - COPD Merck & Co IncExecutive Director, Medical Affairs - COPDNorth Wales, PA$255,800–$402,700 / yearRequired Skills: Chronic Obstructive Pulmonary Disease (COPD), Clinical Development, Clinical Research, Enterprise Leadership, Leadership Management, Medical Affairs, Organizational Leadership, Pharmaceutical Medical Affairs, Resourcing Strategies, Scientific Communications, Strategic Leadership. Collaborates across V&I, including U.S. EDMAs, Regional Leaders, and Outcomes Research, embedding fully within PDT/ADT frameworks to provide subject-matter expertise, drive accountability, and enhance value through effective partnerships.
Director, Engineering - Technical Operations Merck & Co IncDirector, Engineering - Technical OperationsWilmington, DE$173,200–$272,600 / yearAccountable for providing key input into all phases of facility startup-from facility, process, equipment, logistics and utility design to establishing systems and programs for routine manufacturing of cytotoxic and non-cytotoxic compounds, ensuring compliance through validation, operational readiness, and licensing/ launch of new products. Actively partner with Operations, Quality, Supply Chain, Global S&T teams, R&D, GES, and Regulatory Affairs on new product introduction (NPI) to ensure that product quality, availability, and compliance with manufacturing processes are maintained within budget and delivered on time, while also providing support for regulatory filings.
Associate Director - Digital Transformation Merck & Co IncAssociate Director - Digital TransformationNorth Wales, PA$129,000–$203,100 / yearYou are equally comfortable analyzing data, mapping end-to-end user experiences, evaluating system interactions, influencing stakeholders, and building prototype solutions that demonstrate value. Required Skills: Automation Systems, Business Process Development, Business Processes, Business Process Optimization (BPO), Collaboration, Data Analysis, Digital Transformation, Process Automations, Process Improvements, Process Optimization, SAP Systems.
Executive Director, Medical Affairs - COPD Merck & Co IncExecutive Director, Medical Affairs - COPDupper gwynedd, PA$255,800–$402,700 / yearRequired Skills: Chronic Obstructive Pulmonary Disease (COPD), Clinical Development, Clinical Research, Enterprise Leadership, Leadership Management, Medical Affairs, Organizational Leadership, Pharmaceutical Medical Affairs, Resourcing Strategies, Scientific Communications, Strategic Leadership. Collaborates across V&I, including U.S. EDMAs, Regional Leaders, and Outcomes Research, embedding fully within PDT/ADT frameworks to provide subject-matter expertise, drive accountability, and enhance value through effective partnerships.
Executive Director, Medical Affairs - COPD Merck & Co IncExecutive Director, Medical Affairs - COPDRahway, NJ$255,800–$402,700 / yearRequired Skills: Chronic Obstructive Pulmonary Disease (COPD), Clinical Development, Clinical Research, Enterprise Leadership, Leadership Management, Medical Affairs, Organizational Leadership, Pharmaceutical Medical Affairs, Resourcing Strategies, Scientific Communications, Strategic Leadership. Collaborates across V&I, including U.S. EDMAs, Regional Leaders, and Outcomes Research, embedding fully within PDT/ADT frameworks to provide subject-matter expertise, drive accountability, and enhance value through effective partnerships.
Senior Specialist, Nonclinical Medical Writing Merck & Co IncSenior Specialist, Nonclinical Medical WritingSouth San Francisco, CA$131,400–$206,800 / yearRequired Skills: Detail-Oriented, Drug Discovery Process, Medical Writing, Pharmacology, Regulatory Compliance, Regulatory Documents, Regulatory Filings, Regulatory Processes, Regulatory Research, Regulatory Submissions, Scientific Literacy, Scientific Writing, Study Reports, Technical Communication. Key responsibilities: Serve as a central coordinator for generating preclinical reports and regulatory submission modules, manage the overall scope and timeline, and guide the internal review/approval and submission processes, in collaboration with various research and regulatory functions.
Sr. Principal Scientist (Senior Director), Laboratory Lead - Molecular Pathology Merck & Co IncSr. Principal Scientist (Senior Director), Laboratory Lead - Molecular PathologyRahway, NJ$173,200–$272,600 / yearProvide technical oversight of external tissue assay vendors and partner laboratories, including vendor selection and qualification, quality review, performance monitoring, issue resolution, and delivery of fit-for-purpose assay results and documentation. Provide daily laboratory leadership, including work prioritization, capacity planning, sample and reagent readiness, data review, instrument oversight, documentation, and timely delivery of high-quality results.
Senior Principal Scientist, Veterinary Pathology Board Certified Merck & Co IncSenior Principal Scientist, Veterinary Pathology Board CertifiedWest Point, PA$231,900–$365,000 / yearRequired Skills: Analytical Assays, Analytical Assays, Assay Development, Biomedical Sciences, Biotechnology, Clinical Assays, Clinical Data Interpretation, Clinical Judgment, Clinical Safety, Drug Development, Drug Discovery Research, Drug Research, Histopathology, Immunochemistry, Immunology Research, Innovation, In Vitro Research, In Vivo Models, Laboratory Processes, Medical Biology, Molecular Diagnostic Techniques, Pathogenesis, Pharmaceutical Research, Post Mortem Analysis, Safety Pharmacology {+ 3 more}. Our Company's Research Laboratories nonclinical drug safety department at West Point, Pennsylvania site is seeking an experienced anatomic pathologist to join a highly collaborative team of scientists (12 anatomic pathologists, 3 clinical pathologists, and approximately 40 exceptional laboratory scientists), working at a GLP-compliant facility with state-of-the-art anatomic, molecular and clinical pathology laboratories.
Director, US Medical Affairs (US DMA) - Pulmonary Hypertension Merck & Co IncDirector, US Medical Affairs (US DMA) - Pulmonary HypertensionNorth Wales, PA$190,800–$300,300 / yearAs a core member (or co-lead) of the US Medical Affairs Team (MAT), the US DMA collaborates with the Global TA team and cross-functional partners to enable US regional implementation of Value & Implementation (V&I) Planning by: 1) Integrating local insights into Global Scientific Value Content (GSVC) and Center of Scientific Exchange Excellence (CSEE) plans 2) Facilitating local adoption of GSVC and CSEE initiatives 3) Leading development and execution of aligned local training programs 4) Evaluating training effectiveness and application in the field. This position strategically drives scientific excellence across in-line business and the One Pipeline while optimizing field readiness across the USMA strategic pillars: 1.) Scientific Exchange 2.) Company Trials 3.) Investigator-Sponsored Programs 4.) Congresses 5.) Insights.
Principal Scientist, Lab Platform Disruptive Technologies Merck & Co IncPrincipal Scientist, Lab Platform Disruptive TechnologiesCambridge, MA$194,100–$305,600 / yearRequired Skills: Antibody Drug Conjugates (ADC), Biodesign, Detail-Oriented, Emerging Technologies, Ethical Compliance, Gene Cloning, Gene Expression Analysis, Immunochemistry, Leadership Engagement, Mass Spectrometry Analysis, Microscopy Techniques, Project Leadership, Protein Engineering, Protein Interactions, Protein Purifications. This individual will identify and translate emerging, literature-supported technologies into scalable internal capabilities, with a focus on multiplying both the scale and speed of quantitative data generation (e.g., binding measurements) to advance therapeutic programs via GenAI/ML-driven discovery and iterative design-make-test cycles.
US Director Medical Affairs (USDMA): Rheumatology/Dermatology (Remote) Merck & Co IncUS Director Medical Affairs (USDMA): Rheumatology/Dermatology (Remote)North Wales, PARemote$190,800–$300,300 / yearAs a core member (or co-lead) of the US Medical Affairs Team (MAT), the US DMA collaborates with the Global TA team and cross-functional partners to enable US regional implementation of Value & Implementation (V&I) Planning by: 1) Integrating local insights into Global Scientific Value Content (GSVC) and Center of Scientific Exchange Excellence (CSEE) plans 2) Facilitating local adoption of GSVC and CSEE initiatives 3) Leading development and execution of aligned local training programs 4) Evaluating training effectiveness and application in the field. This position strategically drives scientific excellence across in-line business and the One of our company's Pipeline while optimizing field readiness across the USMA strategic pillars: 1.) Scientific Exchange 2.) Company Trials 3.) Investigator-Sponsored Programs 4.) Congresses 5.) Insights.
Senior Director, Pharmacokinetics, Dynamics, Metabolism and Bioanalysis, Protein Therapeutics Merck & Co IncSenior Director, Pharmacokinetics, Dynamics, Metabolism and Bioanalysis, Protein TherapeuticsBoston, MA$194,100–$305,600 / yearRequired Skills: ADME, Assay Development, Bioanalysis, Bioanalytical Assays, Bispecific Antibodies, Communication, Cross-Cultural Awareness, Drug Discovery Development, Drug Metabolism, Fast-Paced Environments, Immunology, Immunotherapy, Innovation, Ligand Binding Assay, Modeling Simulations, Monoclonal Antibodies, Oncology, People Leadership, Pharmacokinetics, PKPD Modeling, Protein Engineering, Results-Oriented, Scientific Leadership, Strategic Thinking, Therapeutic Proteins. The successful candidate will lead a group of principal investigators and subject matter experts and will be expected to collaborate cross-functionally with discovery biologics, nonclinical drug safety, translational medicine and therapeutic area colleagues to ensure robust program strategies from early discovery through to IND submission and beyond.
Associate Principal Scientist, Health Economic and Decision Sciences Merck & Co IncAssociate Principal Scientist, Health Economic and Decision SciencesRahway, NJ$156,900–$247,000 / yearBARDS is responsible for strategic design and analysis to enable informed decision making in the discovery, development and delivery of our Company's innovative products, and is a leader in quantitative scientific methodology and its application to enable the targeting, discovery, development, manufacturing, and marketing of drugs and vaccines for the benefit of patients and global public health. Under the direction of an HEDS Senior Director, the Associate Principal Scientist provides strategic development and use of industry-leading predictive and economic models to enhance our understanding of disease and to quantify and communicate the value of our oncology products to patients, providers, and payers.
Associate Principal Scientist, Health Economic and Decision Sciences Merck & Co IncAssociate Principal Scientist, Health Economic and Decision SciencesBoston, MA$156,900–$247,000 / yearBARDS is responsible for strategic design and analysis to enable informed decision making in the discovery, development and delivery of our Company's innovative products, and is a leader in quantitative scientific methodology and its application to enable the targeting, discovery, development, manufacturing, and marketing of drugs and vaccines for the benefit of patients and global public health. Under the direction of an HEDS Senior Director, the Associate Principal Scientist provides strategic development and use of industry-leading predictive and economic models to enhance our understanding of disease and to quantify and communicate the value of our oncology products to patients, providers, and payers.
Director, Operations Merck & Co IncDirector, OperationsWilmington, DE$173,200–$272,600 / yearThe Director, Operations - Drug Product plays a critical part in strategic project realization of the Wilmington Biotech facility, a new hi-potent facility in our company's Biologic manufacturing network, ensuring that site's mission and objectives are effectively achieved, consistent with our company's requirements to ensure compliance, safety and reliable supply to our customers. You will be accountable for achieving onsite Key Performance Indicators (KPIs), monitoring and striving to improve performance metrics related to hiring, uptime, training, change controls, investigations, CAPAs, yield, volume, production cadence, operational availability, and more.
Clinical Director, Oncology Early Development Merck & Co IncClinical Director, Oncology Early DevelopmentRahway, NJ$255,800–$402,700 / yearThe Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies. The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Early Oncology therapeutic area.
Director, Clinical Research, Obesity Merck & Co IncDirector, Clinical Research, ObesityBoston, MA$255,800–$402,700 / yearWork closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the team in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. The Director (Principal Scientist) has primary responsibility for the planning and directing clinical research activities involving new or marketed medicines in the Metabolism section of the Atherosclerosis & Metabolism therapeutic area, with a focus on obesity and obesity-related disorders.
Associate Director - Digital Transformation Merck & Co IncAssociate Director - Digital TransformationRahway, NJ$129,000–$203,100 / yearYou are equally comfortable analyzing data, mapping end-to-end user experiences, evaluating system interactions, influencing stakeholders, and building prototype solutions that demonstrate value. Required Skills: Automation Systems, Business Process Development, Business Processes, Business Process Optimization (BPO), Collaboration, Data Analysis, Digital Transformation, Process Automations, Process Improvements, Process Optimization, SAP Systems.
Associate Principal Scientist, Combination Product Design Verification (Associate Director Equivalent) Merck & Co IncAssociate Principal Scientist, Combination Product Design Verification (Associate Director Equivalent)Rahway, NJ$142,400–$224,100 / yearRequired Skills: Collaborative Development, Combination Products, Commercialization, Design Controls, Design Failure Mode and Effect Analysis (DFMEA), Design Verification Testing, Device Development, Human Factor Engineering, Manufacturing Processes, Mechanical Engineering, Mechanical Testing, Medical Device Quality Systems, Method Validation, Product Risk Management, Project Leadership, Quality Management Systems (QMS), Release Testing, Self Motivation, Testing Methodology, Test Method Validation, Test Procedure Development, Troubleshooting. This role has a primary focus on design verification while encompassing the full spectrum of testing activities, including test method development and validation, analytical transfers, incoming testing, in-process, release testing, and testing readiness to enable successful clinical introduction and commercialization.