Senior Scientist, Regulatory & Clinical Operations Hims & HersSenior Scientist, Regulatory & Clinical OperationsSouth Plainfield, New JerseyPhD in Clinical Chemistry, Biochemistry, Analytical Chemistry, Molecular Biology, or related field with 4+ years; OR Master’s degree with 7+ years; OR Bachelor’s degree with 10+ years of relevant bench experience in a diagnostic or clinical laboratory setting. The ideal candidate is comfortable operating at the intersection of bench science and clinical study execution, translates regulatory rigor into practical day-to-day decisions, and thrives working independently in a fast-moving environment.
Clinical Specialist II, Cardiac Rhythm Management - Long Island, NY Abbott LaboratoriesClinical Specialist II, Cardiac Rhythm Management - Long Island, NYLong Island, NY$68,000–$136,000 / yearMust have extensive personal computer skills, including experience with Microsoft Office or equivalent software, for tasks such as graphics, word processing, databases, and authoring programs, to develop presentation materials. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.
Clinical Research Associate, Full Time Days 8a-4p, Atlantic Health, Morristown Medical Center Atlantic Health System IncClinical Research Associate, Full Time Days 8a-4p, Atlantic Health, Morristown Medical CenterMorristown, NJAtlantic Health scored four A grades by The Leapfrog Group in its Fall 2025 Hospital Safety Grades, performance measures reflecting errors, accidents, injuries and injections, as well as systems hospitals have in place to prevent harm. Morristown Medical Center is a Magnet Hospital for Excellence in Nursing Service, the highest level of recognition achievable from the American Nurses Credentialing Center for facilities that provide acute care services.
Principal Medical Writer Revolution Medicines IncPrincipal Medical WriterNY$201,000–$251,000 / yearThe company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. Ability to successfully manage and prioritize writing projects with competing deadlines, to foster collaborative cross-functional relationships, and to drive high-quality regulatory writing projects to successful submission.
Principal Biostatistician - Statistical Innovation Regeneron Pharmaceuticals IncPrincipal Biostatistician - Statistical Innovationtarrytown, NY$109,900–$179,300 / yearThe incumbent will work with cross-functional teams to articulate drug development questions, assess the feasibility of endpoints and frame statistical approaches to address those questions, design clinical experiments and interventional studies to generate and analyze the resulting data, and work with teams to appropriately interpret the results and make decisions. This role might be for you if you can: Interact with Global Clinical Operations, Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing, and others to design and analyze clinical trials.
Principal Medical Writer BeOne Medicines AGPrincipal Medical WriterNY$119,300–$159,300 / yearGeneral Description: This position is responsible for providing expertise to support the development of high-quality, fit-for-purpose clinical and regulatory documents to facilitate speed of information during development, submission, approval, and life-cycle management of products in BeiGene pipeline. Essential Functions of the Job: Document Writing: Manages the assigned writing tasks and ensures that the documents adhere to relevant regulatory guideline(s), as well as BeiGene SOP/WI(s), template(s), and style guide.
NewClinical Development Scientist, Senior Manager PfizerClinical Development Scientist, Senior ManagerNew York City, NY$139,100–$231,900 / yearProvides clinical input to the development of the clinical data collection strategy, instruments, and data review plan, ensuring alignment with the protocol and SAP, optimized data collection principles, and clinical data review best practice; performs clinical data review; may present data to internal and external stakeholders; partners with site-facing colleagues in support of data issue resolution; ensures all clinical queries are appropriately addressed in support of database lock. Provides clinical input to the development of the Safety Review Plan and Safety Narrative Plan; reviews safety data and may update clinical documents in response to emerging safety profile; tracks and reconciles Serious Adverse Events; participates in clinical safety data discussion during Safety Review Team meetings in collaboration with Medically Qualified Individual(s); reviews safety narratives.
Machine Learning Scientist, Multimodal AI Natera IncMachine Learning Scientist, Multimodal AINY$124,800–$156,000 / yearCore experience developing machine learning models for biomedical applications, specifically in medical imaging, computational pathology, genomics, transcriptomics, multi-omics, or molecular diagnostics. The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world-class institutions, who care deeply for our work and each other.
Prin. Scientist, Regulatory Liaison Merck & Co IncPrin. Scientist, Regulatory LiaisonRahway, NJ$173,200–$272,600 / yearPrimary activities include, but are not limited to: Functions with a high degree of independence and provides regulatory oversight for assigned products, functioning as the single, accountable, global regulatory point of contact on those projects within Global Regulatory Affairs and Clinical Safety (GRACS) and external to GRACS. Represents Global Regulatory Affairs (GR) within internal committees to provide regulatory advice and approval according to the committee charters (therapeutic area Document Review Committees, Product Development Team, Early Development Team, and Label Evaluation and Development Team.
NewAssoc Principal Scientist Statistical Programming, Late-Stage (Non-Oncology) (Hybrid) Merck & Co IncAssoc Principal Scientist Statistical Programming, Late-Stage (Non-Oncology) (Hybrid)Rahway, NJ$142,400–$224,100 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Education and Minimum Requirement: BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 9 years SAS programming experience in a clinical trial environment.
Senior Scientist, Statistical Programming, Late-Stage Oncology (Hybrid) Merck & Co IncSenior Scientist, Statistical Programming, Late-Stage Oncology (Hybrid)Rahway, NJ$117,000–$184,200 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our Company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Education and Minimum Requirement: BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 5 years SAS programming experience in a clinical trial environment.
Principal Scientist, Large Molecule Analytical Merck & Co IncPrincipal Scientist, Large Molecule AnalyticalRahway, NJ$156,900–$247,000 / yearThe Principal Scientist is a highly visible and impactful senior scientific role tasked with working closely with the group Director to define analytical strategy and to lead a team of scientists in solving complex analytical problems at the interface of biology, chemistry, and lab informatics disciplines to enable development of biologics active pharmaceutical ingredients (APIs). Required Skills: Analytical Method Development, Assay Development, Bioanalytical Analysis, Chromatographic Techniques, Clinical Judgment, Cross-Functional Teamwork, Dosage Forms, Ethical Compliance, Liquid Chromatography (LC), Matrix Management, Mentoring Staff, Method Validation, Personal Initiative, Stability Testing, Technical Writing.
Scientist II or III - Metrology Specialist - FSP Parexel International CorpScientist II or III - Metrology Specialist - FSPNJFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. Experience maintaining, operating, and troubleshooting laboratory equipment including High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Ultraviolet-Visible spectroscopy (UV-Vis), dissolution systems, and other specialized computerized systems.
Principal Scientist, Upstream Process Development Merck & Co IncPrincipal Scientist, Upstream Process DevelopmentRahway, NJ$173,200–$272,600 / yearBackground in data science approaches related to cell culture and predictive modeling e.g., metabolic flux analysis (MFA), omics, machine learning; experience integrating PAT efforts) and computational fluid dynamics (CFD). Providing technical direction for process development, characterization, commercialization, and regulatory filing activities to ensure a smooth and clear path to successful PPQs an BLAs for our company pipeline.
Scientist II or III Analytical Chemist (Drug Product) - FSP Parexel International CorpScientist II or III Analytical Chemist (Drug Product) - FSPNJFor results-driven and caring individuals who want to make a meaningful difference in the world, Parexel is trusted by life sciences companies to meet their long-term staffing needs for scientists and engineers and related professionals in discovery and development of novel therapies, keeping patients at the center of everything we do, and where an inclusive community helps you be your best, transforming any career into a life-changing achievement. In the drug product registration stability testing lab, you'll perform routine and stability sample analysis, SOP authoring, and day-to-day problem solving while contributing to new technologies and continuous improvement measures for optimized lab operations and other testing requirements.
Principal Scientist, Oral Formulation Sciences Merck & Co IncPrincipal Scientist, Oral Formulation SciencesRahway, NJ$173,200–$272,600 / yearIn this role, the individual will be responsible for leading CMC project teams and the formulation development of new chemical entities through a matrix team from initial first in human formulations (suspensions, solutions, capsules, tablets) through final market formulation definition and manufacturing process robustness assessment. Principal Scientist Job Description: Our company's Pharmaceutical Sciences and Clinical Supply (PSCS) organization translates molecules to medicines, working from the discovery interface through registration stability manufacturing by designing, developing and scaling-up the formulation, device, and manufacturing process.
Director, Program Lead - Immunology Merck & Co IncDirector, Program Lead - ImmunologyRahway, NJ$173,200–$272,600 / yearRequired Skills: Clinical Leadership, Clinical Programs, Clinical Strategy, Clinical Trials Operations, Coaching, Cross-Functional Leadership, Good Clinical Practice (GCP), Immunology, People Management, Program Management, Project Management, Scientific Leadership, Stakeholder Communications, Vendor Oversight. Ideal candidate would have: Highly preferred: Experience in conducting global clinical trials programs, including product planning through initial filing in Gastroenterology, Dermatology, or Rheumatology, especially autoimmune or immune-mediated disorders (e.g., ulcerative colitis, Crohn's disease, rheumatoid arthritis, hidradenitis suppurative, atopic dermatitis, etc.).
Associate Principal Scientist (Associate Director), Outcomes Research, Pediatric Vaccines Merck & Co IncAssociate Principal Scientist (Associate Director), Outcomes Research, Pediatric VaccinesRahway, NJ$156,900–$247,000 / yearRequired Skills: Biology, Comparative Effectiveness Research, Conference Presentations, Data Management, Epidemiological Research, Epidemiologic Methods, Epidemiology, Health Economics, Health Services Research, Medical Procedures, Meta-Analysis, Outcomes Research, Pharmacoeconomics, Research Designs, Researching, Retrospective Analysis, Scientific Research, Scientific Writing, Stakeholder Relationship Management, Strategic Planning. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, health-care resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling.
Medical Laboratory Scientist ICONMA, LLCMedical Laboratory ScientistClifton, NJ$30–$40 / hourFollow the laboratory's procedures for specimen handling and processing, test analyses, reporting and maintaining records of patient test result; Maintain records that demonstrate that proficiency testing samples are tested in the same manner as patient specimens; Analyze specimens using approved testing procedures (see department SOPs). Adhere to the laboratory's quality control policies, document all quality control activities, instrument and procedural calibrations and all maintenance performed; Follow the laboratory's established policies and procedures whenever test systems are not within the laboratory's established acceptable levels of performance.
Senior Data Scientist - SFL Scientific Deloitte Touche Tohmatsu LtdSenior Data Scientist - SFL ScientificNew York, NY$128,000–$252,500 / yearWorking with a team of interdisciplinary data scientists, engineers, architects, and consultants, our work includes novel areas such as cancer detection, drug discovery, optimizing population health and clinical trials, autonomous systems and edge AI, agentic solutions, and consumer product innovation. From strategy to execution, this team delivers integrated, end-to-end support and advisory services covering valuation modeling, cost optimization, restructuring, business design and transformation, infrastructure and real estate, mergers and acquisitions (M&A), and sustainability.