Senior Clinical Lead, Early Clinical & Experimental Therapeutics SanofiSenior Clinical Lead, Early Clinical & Experimental TherapeuticsMorristown, NJ$236,250–$341,250 / yearIn these roles, duties include: Design safe, rapid and informative First-In-Human studies for oncology assets potentially including natural history, experimental model validation, mechanistic and signal seeking, streamlined Proof-of-Mechanism as well as Proof-of-Concept studies providing robust data for early Go/No Go decisions and other pharmacokinetic studies. A key focus of this role is to support the path from the research phase through early clinical development including early and rapid Proof-of-Mechanism/Proof-of-Concept, as well as natural history studies and experimental model validation to contribute to Human Target Validation (HTV) and evaluating the pharmacology of novel therapeutic approaches.
Senior Scientist, R&D - Assay Development hims & hersSenior Scientist, R&D - Assay DevelopmentSouth Plainfield, NJYou Have: PhD 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. This individual contributor will report to the Director of R&D and work closely to develop and validate diagnostic assays supporting both traditional and at-home testing programs, and support assay implementation into clinical operations.
Senior Scientist, Analytical Development & Quality Control Protagonist TherapeuticsSenior Scientist, Analytical Development & Quality ControlNewark, New JerseyThe successful candidate will help drive analytical development strategy for small-molecule and peptide candidates from early development through late-stage programs, including analytical method development, validation, transfer, stability programs, phase-appropriate specifications, and analytical control strategies for drug substance (DS) and drug product (DP). The Company also has a number of clinical and preclinical programs based on clinically and commercially validated targets and addressing unmet medical needs, including an oral IL-17 antagonist peptide, anti-obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin discovery programs.
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.
Associate Principal Scientist, Upstream Development Merck & Co IncAssociate Principal Scientist, Upstream DevelopmentRahway, NJ$142,400–$224,100 / yearRequired Skills: Biodesign, Biodesign, Biological Engineering, Cell Cultures, Cell Line Development, Cell Physiology, Chemical Engineering, Clinical Trials, Computational Fluid Dynamics (CFD), Detail-Oriented, Downstream Process Development, Drug Delivery Technology, Drug Development, Expression Vectors, Interpersonal Relationships, Leading Project Teams, Mammalian Cell, Mammalian Cell Culture, Manufacturing Processes, Molecular Biology, Operational Efficiency, Pharmaceutical Formulations, Pharmaceutical Process Development, Physical Characterization, Stable Cell Lines {+ 1 more}. In this role, the successful candidate will work closely with a highly motivated team of Scientists and Engineers in the Upstream Process Development area and contribute to CMC development of our company's pipeline, playing an active role in the design, development, and optimization of cell culture processes and the transfer of processes to clinical and commercial manufacturing sites.
Principal Scientist, Biostatistics Merck & Co IncPrincipal Scientist, BiostatisticsRahway, NJ$190,800–$300,300 / 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. This position involves interaction with Medical, Data Coordination, Statistical Programming, our Research & Development Division scientists and Regulatory staffs in designing and analyzing clinical trials and coordinating the statistical activities for clinical trial projects; and may lead a group of statistical or programming staff assigned to a development project as needed.
Senior Scientist, Statistical Programming Merck & Co IncSenior Scientist, Statistical ProgrammingRahway, NJ$117,000–$184,200 / yearRequirements: Must have a Master's degree (or US equivalent) in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 3 years experience in SAS programming in a clinical trial environment OR a Bachelor's degree (or US equivalent) in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 5 years experience in SAS programming in a clinical trial environment. Required Skills: Clinical Development, Clinical Trials, Computer Science, Data Management, Data Modeling, Global Health, Marketing, Numerical Analysis, Outcomes Research, Project Leadership, Stakeholder Engagement, Stakeholder Relationship Management, Statistical Analysis, Statistical Programming, Strategic Thinking, Waterfall Model, Working Independently.
Principal Scientist, Upstream Development Merck & Co IncPrincipal Scientist, Upstream 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). In this role, the successful candidate will work closely with scientists in the Upstream Development Department to develop and refine technical strategy related to next generation processing for assets in early- and late-stage clinical development.
Principal Scientist, Long-Acting Injectable Sterile Product Development Merck & Co IncPrincipal Scientist, Long-Acting Injectable Sterile Product DevelopmentRahway, NJ$173,200–$272,600 / yearServe as a principal-level LAI formulation scientist, providing scientific leadership for the design, development, and lifecycle management of long-acting injectable drug products, including depot, sustained-release, and controlled-delivery parenteral dosage forms. This role is a Principal Scientist-level technical leadership position with a primary focus on long-acting injectable drug products, including depot formulations, extended-release systems, and injectable sustained-delivery technologies.
Associate Principal Scientist, Long-Acting Injectable Sterile Product Development Merck & Co IncAssociate Principal Scientist, Long-Acting Injectable Sterile Product DevelopmentRahway, NJ$142,400–$224,100 / yearRequired Skills: Bioprocess Engineering, Bioprocess Engineering, Cell Line Development, Chemical Engineering, Downstream Process Development, Drug Delivery, Drug Delivery Technology, Drug Development, Drug Formulations, Early Phase Clinical Trials, Expression Vectors, Kinetics, Molecular Biology, Pharmaceutical Formulations, Pharmaceutical Process Development, Pharmaceutical Products, Pharmaceutical Research, Pharmaceutical Sciences, Pharmaceutical Technologies, Pharmaceutics, Physical Characterization, Product Development Lifecycle, Product Formulation, Regulatory Submissions, Stable Cell Lines {+ 1 more}. This role is an Associate Principal Scientist-level technical leadership position with a primary focus on long‑acting injectable drug products, including depot formulations, extended‑release systems, and injectable sustained‑delivery technologies.
NewAssociate Principal Scientist, Statistical Programming, Late-Stage Oncology (Hybrid) Merck & Co IncAssociate Principal Scientist, Statistical Programming, Late-Stage 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. Required Skills: Base SAS, Clinical Development, Data Management, Data Modeling, FDA Submissions, Influencing Skills, Oncology, Presentation Delivery, Process Improvements, Project Management, Project Planning, Resource Planning, Stakeholder Management, Statistical Programming, Strategic Planning, Strategic Thinking.
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.
Medical LAB Scientist (Per Diem) - Temple Health/Chestnut Hill Hospital Temple University Health SystemMedical LAB Scientist (Per Diem) - Temple Health/Chestnut Hill HospitalPhiladelphia, PABachelor's Degree Medical Technology, Biological Sciences, Chemistry, or Life Sciences with 26 science credits with appropriate experience in a CLIA laboratory Required. The MLS works independently, organizing work to meet established deadlines and validates all data obtained.
Scientist II, Formulation Development PTC TherapeuticsScientist II, Formulation DevelopmentBridgewater, NJ$133,100–$158,000 / yearMinimum level of education and years of relevant work experience: PhD degree in pharmaceutical science, material science, chemistry or other related scientific discipline with minimum 2 years of relevant experience OR Master's degree in these same disciplines with min 4 years of relevant experience OR a Bachelor's degree in these same disciplines and a minimum of 6 years of relevant experience in discovery formulation, pre-formulation or formulation development in a pharmaceutical, biotechnology or other related environment. Special knowledge or skills needed and/or licenses or certificates required: Hands-on experience and demonstrated proficiency with basic laboratory skills, design, development, and characterization of liquid and solid dosage forms using formulation equipment such as blenders, granulators, roller compactors, tablet presses, coaters, fluid-bed dryers etc.
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 Principal Scientist, Global Regulatory Lead Organon & CoAssociate Principal Scientist, Global Regulatory LeadFlorham Park, NJ$125,400–$213,100 / yearRepresent our company with external organizations through direct communication with the FDA, EMA, or other EU regulatory agencies, including telephone calls and e-mail; chair meetings between company and FDA or EMA; prepare our company's teams for meetings with FDA or EMA at any phase of drug development. Associate Principal Scientist, Global Regulatory Lead reporting to the Executive Director, Fertility Lead will be responsible for the development and implementation of world-wide regulatory strategies, including CMC elements, for the medical devices and combination products (MDCP) portfolio.
Staff Scientist II - Medicinal Chemistry Protagonist TherapeuticsStaff Scientist II - Medicinal ChemistryNewark, New JerseyStrong verbal and written communication skills The base pay range for this position at commencement of employment is expected to be between $135,000 and $145,000/year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The Company also has a number of preclinical stage drug discovery programs addressing clinically and commercially validated targets including an oral IL-17 peptide antagonist, obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin programs.
Scientist III - Peptide Synthesis Discovery Chemistry - FSP Parexel International CorpScientist III - Peptide Synthesis Discovery Chemistry - 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. Under direction and guidance of the scientific supervisor or more senior group members: Execute any aspects (synthesis, workup, purification, analysis) of routine peptide preparations in a range of scales and demonstrate flexibility and rapid pace in moving across this space.
Biologics Process R&D Senior Scientist Merck & Co IncBiologics Process R&D Senior ScientistRahway, NJ$117,000–$184,200 / yearMINIMUM EDUCATION REQUIREMENTS: B.S. with 4 years, or M.S. with 3 years or PhD with 0+ years of relevant experience (or expected PhD graduation by June 2027) in Chemical Engineering, Biochemical Engineering, Biomedical Engineering, Biotechnology, Biochemistry, Biology, Microbiology, or related fields. Biologics Process Research & Development (BPR&D) within our Research & Development Division is on a mission to rapidly deliver diverse biotherapeutics to patients by efficiently developing innovative, robust manufacturing processes and technologies.