Director, Study Quality and Compliance - Nonclinical Safety/Toxicology Novartis AGDirector, Study Quality and Compliance - Nonclinical Safety/ToxicologyEast Hanover, NJ$185,500–$344,500 / yearThis team is responsible for: handling samples and data associated with both internally and externally conducted toxicology studies; maintaining departmental SOPs, and oversight of training records for departmental personnel; and interfacing with the archives function to ensure proper storage of toxicology-related materials and records. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-cultureBenefits and Rewards: Learn about all the ways we'll help you thrive personally and professionally.
Principal Scientist I/II, Study Quality and Compliance - Nonclinical Safety/Toxicology Novartis AGPrincipal Scientist I/II, Study Quality and Compliance - Nonclinical Safety/ToxicologyEast Hanover, NJ$119,700–$222,300 / yearEssential Requirements: Degree in biological related sciences8+ years of relevant experience working in a pharmaceutical settingExperience working in GLP setting, and general regulatory compliance and animal welfare knowledge related to conduct of toxicology studiesGood communication skills, and excellent logistical/planning skillsFluent in English (spoken and written)Desirable Requirements: Previous experience with SEND packages is desirablePrevious experience with software for online information and program management is a plusThis is a dual level posting. Support SEND package creation and quality review for FDA submissionsSupport the Study Quality and Compliance team's effort for tracking and managing study-related information through input of information types from the areas of responsibility above and generally support the effort in various workstreams or initiatives.
Principal Scientist, Toxicology PTC TherapeuticsPrincipal Scientist, ToxicologyBridgewater, New JerseyHe/she will interact within the organization to communicate relevant safety information and act as a toxicology representative in interactions with Project teams, Collaborators, and Contract Research Organizations (CROs). Writes/Prepares regulatory documents including Toxicology sections of briefing books, investigational new drug applications (INDs), and investigator brochures (IBs).
Certifying Scientist -Toxicology (ToxAssure) Labcorp Holdings IncCertifying Scientist -Toxicology (ToxAssure)Raritan, NJ$32.50–$44 / hourJob Responsibilities: Review all test results for applicable screening and confirmatory clinical toxicology testing methodologies, relevant Quality Control data and associated documentation. If you are an individual with a disability who needs assistance using our online tools to search and apply for jobs, or needs an accommodation, please visit our accessibility site or contact us at Labcorp Accessibility.
Senior Scientist II, Product Safety & Toxicology, L''Oréal Research & Innovation L'Oreal USA IncSenior Scientist II, Product Safety & Toxicology, L''Oréal Research & InnovationNJResearch & Innovation. 22-Apr-2026.
Associate Director, Toxicology Protagonist TherapeuticsAssociate Director, ToxicologyNewark, New JerseyThe 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. Associate Director, Toxicology, Nonclinical Development (Program Toxicologist) Position Description: Protagonist Therapeutics is seeking a talented, highly motivated professional to join the Toxicology, Nonclinical Development team as Associate Director Toxicology, Nonclinical Development (Program Toxicologist).
Senior Scientist II Occupational & Environmental Toxicologist AbbVie IncSenior Scientist II Occupational & Environmental ToxicologistNJScientist II Qualifications: Bachelor's Degree in toxicology or related discipline and typically 12 years of experience OR Master's Degree in toxicology or related discipline and typically 10 years of experience OR PhD in toxicology or related discipline and typically 4 years of experience. This includes toxicology support for extractables and leachables, health-based exposure limits (HBELs) including permitted daily exposure limits (PDEs) and occupational exposure limits (OELs), environmental risk assessments (ERA), and other contaminants.
Project Manager, Discovery & Preclinical Development Protagonist TherapeuticsProject Manager, Discovery & Preclinical DevelopmentNewark, New JerseyThe 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. The base pay range for this position at commencement of employment is expected to be between $160K and $185K a year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.
Associate Director, Pharmacovigilance/ Product Safety Insmed IncAssociate Director, Pharmacovigilance/ Product SafetyNJRemote$179,000–$232,500 / yearFor New York City Residents: To assist in identifying candidates with qualifications matching those required and/or preferred for this role, Insmed uses an Automated Employment Decision Tool ("AEDT") that employs artificial intelligence to analyze and score information provided in resumes and application materials including, but not limited to, skills, work experience, education, and job-related qualifications. Author, review and provide input and approval for drug-safety related regulatory reports and clinical study documents including clinical study protocols, Informed Consent Forms, Investigator Brochures, Integrated Summary of Safety (ISS), Integrated Summary of Efficacy (ISE), MedDRA coding of AEs, product package and labeling.
Distinguished Scientist, Safety Assessment Project Expert SanofiDistinguished Scientist, Safety Assessment Project ExpertMorristown, NJ$178,500–$257,833.33 / yearThese activities entail formulating the nonclinical safety strategies, designing safety pharmacology and toxicology studies, authoring regulatory documents, being a member of an integrated Project Team, interacting with internal and external partners, and interacting with and responding to global regulatory agencies. Our Team: The candidate will be part of a dynamic interactive Preclinical Safety group that spans all aspects of the drug development value chain providing toxicology and safety pharmacology expertise as a member of global project teams.
Associate Chemist City of New YorkAssociate ChemistNYThe Associate Chemist will play an integral role in laboratory testing and responding to public health threats, including but not limited to COVID-19, vaccine preventable diseases, HIV, Legionella as well as respiratory, foodborne, and waterborne disease outbreaks. A baccalaureate degree from an accredited college, including or supplemented by 16 semester credits in chemistry and 8 semester credits in any one or a combination of the following areas: chemistry, pharmacology, toxicology, environmental science, forensic science, or other natural science.
Assistant Professor- Tenure Track - Sustainable Biology and Environmental Science Seton Hall University, New JerseyAssistant Professor- Tenure Track - Sustainable Biology and Environmental ScienceSouth Orange, New JerseyMore specifically, the hire would be expected to (1) run a core biology courses & support the biology majors in all sciences; (2) increase the variety of upper-level bio-electives by offering new courses such as Sustainable Agriculture and Habitat Restoration or Environmental Toxicology and participate in the ongoing creation of academic programs in Environmental Science; (3) assist with educating, managing, mentoring, and advising the increased number of biology majors; (4) provide a computational based research space for undergrads and graduate students; (5) assist with all the day today activities that are important to a functional department; and (6), just as importantly, the faculty member will participate in innovative, collaborative program development in interdisciplinary STEM fields as part of our “STEM Initiative.” Seton Hall University invites applications for a full-time tenure track professor at the rank of Assistant Professor in the Department of Biological Sciences to start Fall 2026, pending final budgetary approval.
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.