Senior Clinical Director, Clinical Research, Hematology Merck & Co IncSenior Clinical Director, Clinical Research, HematologyRahway, NJ$282,200–$444,200 / yearThe Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area, specifically in our Hematology Section. The Senior 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.
Principal Biostatistician/Senior Principal Biostatistician Precision Medicine Group LLCPrincipal Biostatistician/Senior Principal BiostatisticianNY$147,300–$243,000 / yearSpecific responsibilities include consulting with clients regarding clinical trial study design and regulatory strategy, writing and reviewing statistical methods and sample size sections of protocols, writing and reviewing statistical analysis plans of complex study designs, reviewing statistical analyses and presenting statistical results. Qualifications: Minimum Required: Senior Principal Biostatistician level: Master''s degree or equivalent in Statistics, Biostatistics, or related field with 12+ years of experience; PhD degree in Statistics, Biostatistics, or related field with 9+ years of experience.
Data Operations & Domain Manager CBRE Group IncData Operations & Domain ManagerNew York City, NYWhat You Need: At least five years of hands-on experience with asset data in real estate investment management, a REIT, commercial real estate service provider with strong familiarity with the data structures, terminology and complexity inherent in real assets private equity. Working closely with the Asset Domain Data Trustee and sub-domain trustees, and in collaboration with the investment operations, data governance and technology teams, you will build deep expertise in the domain's business use and technical landscape, and influence how confidently the firm acts on its data.
Senior Principal Scientist, Clinical Research, Immunology Merck & Co IncSenior Principal Scientist, Clinical Research, ImmunologyRahway, NJ$282,200–$444,200 / yearWork closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. Required Skills: Clinical Development, Clinical Medicine, Clinical Research Management, Clinical Studies, Clinical Trial Development, Clinical Trials, Dermatology, Drug Development, Gastroenterology, Inflammatory Bowel Diseases, Pharmaceutical Industry, Regulatory Compliance, Rheumatology.
Financial Institution Associate Claim Counsel The Travelers Companies IncFinancial Institution Associate Claim CounselManhattan, NY$89,800–$148,300 / yearFollow operational policies to analyze, investigate, and resolve Financial Institution liability claims involving bank, asset management and insurance company accounts of varying levels of severity with active supervision from claims management. Prepare and present reports for management that accurately reflect loss development, potential/actual financial exposure, reserve adjustments, coverage issues, and claim and recovery strategies.
Scientist (2nd Shift) - Pharmaceutical Analytical Sciences (Onsite) Merck & Co IncScientist (2nd Shift) - Pharmaceutical Analytical Sciences (Onsite)Rahway, NJ$87,300–$137,400 / yearEducation Minimum Requirements: Minimum 3 years relevant industry experience for applicants with a Bachelor of Science degree, or 1 year of relevant industry experience for applicants with a Master of Science degree in Chemistry, Pharmaceutical Sciences, or other Life Sciences. Primary Responsibilities: Support execution of Good Manufacturing Practices (GMP) activities such as release and stability testing to support development of active pharmaceutical ingredients (APIs), pharmaceutical formulations, and manufacturing processes using both traditional and advanced analytical tools.
Implementation Consultant (Remote) Medidata Solutions IncImplementation Consultant (Remote)New York, NYRemote$79,500–$106,000 / yearCelebrating over 25 years of ground-breaking technological innovation across more than 38,000 trials and 12 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and one of the largest clinical trial data sets in the industry. More than 1 million registered users across approximately 2,300 customers trust Medidata's seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster.
NewAssoc Prin Scientist, Outcomes Research Merck & Co IncAssoc Prin Scientist, Outcomes ResearchRahway, NJ$156,900–$247,000 / yearUnder the guidance of a senior leader, an Associate Principal Scientist/Associate Director, has primary responsibility for planning/managing real world and economic evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling.
Senior Principal Statistician, Biometrics Ferring Pharmaceuticals, Inc.Senior Principal Statistician, BiometricsParsippany, NJ$191,000–$225,000 / yearResponsibilities: Evidence generation and real-world evidence (RWE) Supporting the design, conduct, analysis and reporting of RWE studies Contribute to integrated evidence generation strategies combining clinical trial and real-world data Supporting use of RWE in regulatory submissions, health technology assessment (HTA), and lifecycle planning Clinical development and statistical contribution Providing statistical input to clinical development plans and target product profiles Authoring statistical analysis plans and contributing to study design Supporting analysis and interpretation of clinical trial data Contributing to clinical study reports and regulatory submissions Assessment of business development opportunities Critically review and evaluate clinical trial data to assess efficacy, safety, and asset value, including opportunities for life cycle management such as label expansion, new indications, and geographic growth. Requirements: Bachelor’s degree required, Master’s degree or PhD in Statistics, Biostatistics, or a related quantitative field preferred 5+ years of experience working in the pharmaceutical industry· Proficiency in statistical programming languages (e.g., R, SAS)· Experience working with registry/claims data, including assessing the suitability and quality of such data sources in accordance with FDA guidance, and applying methodologies for analyzing observational data, e.g.
Senior Engineer, Facility Operations (On-site) Merck & Co IncSenior Engineer, Facility Operations (On-site)Rahway, NJ$117,000–$184,200 / yearEducation: Bachelor's degree in chemical/biochemical engineering, pharmaceutical sciences, chemistry, biochemistry, biology, microbiology, or related discipline with minimum of 5 years relevant experience, or a Master's degree with minimum 3 years of relevant experience. It can meet all historic, currently existing, and cutting-edge biologics program demands from supporting development to pilot scale, small and large scale potent material handling, and the ability to integrate new technologies and cell-line platforms.
Instrument Consultant (Remote) Medidata Solutions IncInstrument Consultant (Remote)New York, NYRemote$79,500–$106,000 / yearCelebrating over 25 years of ground-breaking technological innovation across more than 38,000 trials and 12 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and one of the largest clinical trial data sets in the industry. About the Team: Responsible for the overall relationship management of Instrument partners and day to day instrument activities to ensure that Medidata is able to deliver quality projects and services on time and within budget through effective management of Medidata resources.
Principal Scientist, Pharmaceutical Analytical Sciences Merck & Co IncPrincipal Scientist, Pharmaceutical Analytical SciencesRahway, NJ$156,900–$247,000 / yearRequired Skills: Analytical Characterization, Analytical Chemistry, Analytical Method Development, Assay Development, Bioanalysis, Chromatographic Techniques, Chromatography, Clinical Judgment, Clinical Trials, Conducting Experiments, Data Science, Liquid Chromatography (LC), Matrix Management, Mentoring Staff, Method Validation, Product Development, Scientific Study Design, Stability Testing. Your main responsibilities, in not particular order and by no means complete, include: Driving our company's Pipeline: Leading analytical teams driving the development of drugs in our company's pipeline, with a deep understanding of product development from early stage through commercialization.
Director, Chemical Engineering R&D Merck & Co IncDirector, Chemical Engineering R&DRahway, NJ$173,200–$272,600 / yearRequired Skills: Chemical Engineering, Chemical Technology, Clinical Manufacturing, Collaborative Communications, Diversity and Inclusion (D&I), Drug Development, Good Manufacturing Practices (GMP), Pharmaceutical Process Development, Pharmaceutical Process Engineering, Process Manufacturing, Project Portfolio Management (PPM), Regulatory Compliance, Technical Leadership, Technology Transfer, Vaccine Manufacturing. Critical tasks involve technical and strategic oversight of chemical engineering staff who directly contribute to the development, characterization and scale-up of various unit operations for manufacturing processes, including batch and continuous reactions, crystallizations, extractions, membrane separations, distillation, filtration and drying.
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.
Associate Director, Outcomes Research Merck & Co IncAssociate Director, Outcomes ResearchRahway, NJ$156,900–$247,000 / yearUnder the guidance of a senior leader, an Associate Principal Scientist/Associate Director, has primary responsibility for planning/managing real world and economic evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling.
Associate Principal Scientist, Analytical R&D Merck & Co IncAssociate Principal Scientist, Analytical R&DRahway, NJ$142,400–$224,100 / yearJoin us and experience our culture firsthand - one of strong ethics & integrity, diversified experiences, exceptional science and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. Your main responsibilities will include: Driving Pipeline: Leading or participating on analytical teams driving the development of drugs in the company's pipeline, with a deep understanding of product development from early stage through commercialization.
Senior Regulatory Affairs Program Manager ImmunityBio IncSenior Regulatory Affairs Program ManagerSummit, NJLead the design, planning, and execution of complex, cross-functional regulatory programs and strategic initiatives, establishing integrated project plans, timelines, milestones, deliverables, resource allocation, and proactive risk-mitigation strategies to ensure successful outcomes. ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells.
Scientist, Analytical R&D Merck & Co IncScientist, Analytical R&DRahway, NJ$87,300–$137,400 / yearWithin the Global Quality Large Molecule Analytical Sciences (GQ- LMAS) organization, this Analytical Transfer Team includes activities interfacing with a global network of product manufacturing and testing sites, collaborating with product development groups within our our company Manufacturing Division and our our company's Research Laboratories division, continuous improvement of analytical methodology, assay validation, analytical technical transfer, and Biologics License Application preparation. Global Quality Large Molecule Analytical Sciences (GQ-LMAS), in our company's Manufacturing Division, is accountable for the commercialization of large molecule, vaccines and biologics, analytical techniques from Phase III through launch and transfer to supply.
Operations, Planning & Administration Manager Verlagsgruppe Georg von Holtzbrinck GmbHOperations, Planning & Administration ManagerNew York, NY$70,000–$80,000 / yearU.S. publishers include Celadon Books, Farrar, Straus and Giroux, Flatiron Books, Henry Holt & Company, Macmillan Audio, Macmillan Children's Publishing Group, The St. Martin's Publishing Group, and Tor Publishing Group. Holtzbrinck Publishing Group's publishing companies include prominent imprints around the world that publish a broad range of award-winning books for children and adults in all categories and formats.
Sr. Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (Onsite) Merck & Co IncSr. Specialist, Process Engineering - Oral Solid Dosage, Clinical Manufacturing (Onsite)Rahway, NJ$117,000–$184,200 / yearThe Non-Sterile Process Engineering team ensures right-first-time manufacture and delivery of high-quality drug products (spray-dried intermediates, tablets and capsules), leveraging pharmaceutical unit operations such as spray-drying, hot-melt extrusion, blending, roller compaction, encapsulation, compression, and film coating. Bachelor of Science degree in Chemical Engineering, Biomedical Engineering, Chemistry, Pharmaceutical Sciences or related scientific field with minimum of 5 years relevant experience, or a Master's degree with 3 years of relevant experience, or a PhD degree (with expected completion no later than June 2026).