Lead Preclinical Safety Scientist — Toxicology & Regulatory
$178.5k - $257.83kSanofi
Sanofi is seeking a Preclinical Safety Toxicologist to support research and development by designing and interpreting toxicology studies. The role requires strategic planning of nonclinical safety programs and providing scientific leadership. Candidates should hold a PhD or DVM in relevant fields with a minimum of 12 years of pharmaceutical industry experience. The job offers a competitive salary between $178,500.00 and $257,833.33, based on experience, along with comprehensive benefits including healthcare and parental leave. #J-18808-Ljbffr Sanofi
- ...Digital Health is looking for a skilled toxicologist to join our Preclinical Safety group in Cambridge, MA. You will oversee the nonclinical... .... Excellent presentation and writing skills are essential as well as experience in regulatory submissions. #J-18808-Ljbffr...Regulatory
- ...Cambridge, MA is looking for a Senior Scientist in Toxicology to lead the pre-clinical safety strategy for oligonucleotide... ..., reporting to the Head of Preclinical Development. The ideal candidate... ...and preparing reports for regulatory submissions. Join a dynamic team...Regulatory
- ...Placement is seeking a highly motivated Senior Scientist in Toxicology in Cambridge, MA. This role offers the opportunity to shape preclinical safety strategies for oligonucleotide programs... ...CRO relationships and authoring regulatory submissions. Join a dynamic team and...Regulatory
- ...USA) is seeking a Senior Toxicologist to lead nonclinical development programs with... ...knowledge of GLP regulations and FDA/ICH safety guidelines, with primary responsibility... ..., interpreting, and reporting regulatory toxicology studies and related pharmacology work in...Regulatory
- Sanofi is seeking a Global Project Head, Toxicology in Cambridge, MA to lead the preclinical safety portfolio. You will guide a team of toxicologists, shape strategy, and partner across Clinical Development, Regulatory Affairs, and DMPK to ensure high-quality submissions...Regulatory
$114.1k - $211.9k
...Cambridge MA Internal: Principal Scientist I or II LI#-Hybrid The Preclinical Safety (PCS) department within the... ..., with state-of-the-art regulatory compliance. As a Preclinical... ...Advanced Degree in Pharmacology, Toxicology or a Related Field ~5+ years...RegulatoryLocal area- ...company in Boston is seeking a Head of Preclinical Toxicology to lead preclinical toxicology activities. The ideal... .... Responsibilities include developing safety strategies and managing external contracts, with a focus on regulatory compliance and innovative therapeutic...Regulatory
$119.7k - $222.3k
...Principal Scientist I/IILI Location: Cambridge MA Internal: Hybrid The... ...and Compliance group within the Toxicology line function of Preclinical Safety (PCS). Key areas of responsibility... ...working in GLP setting, and general regulatory compliance and animal welfare...RegulatoryPermanent employment- BioSpace in Cambridge, MA, is seeking a Preclinical Safety Project Team Member with extensive experience in nonclinical safety strategies and regulatory documentation. The role includes formulating safety strategies for various modalities, ensuring scientific standards...Regulatory
- ...highly motivated Senior Scientist in Toxicology to help drive the pre‑clinical safety strategy for the... ...Reporting to the Head of Preclinical Development, this role... ...serve as Study Director, leading toxicology study... ...document sections for regulatory submissions. Qualifications...Regulatory
- Team Overview Our dynamic Preclinical Safety group spans all aspects of the drug development value chain, providing toxicology and safety pharmacology expertise as a member of global... ...Plans, Scientific Advice, and other regulatory documents; review internal and external...Regulatory
- ...Inc in Boston is searching for a Toxicology Lead to guide nonclinical safety and toxicology work for drug candidates... ...development teams, and handling regulatory submissions. The ideal candidate... ...with significant experience in preclinical toxicology and drug development....Regulatory
- ...Therapeutics is looking for a Toxicology Lead in Boston, MA. The... ...direct nonclinical safety and toxicology for... ..., and contribute to regulatory filings. A PhD or DVM... ...significant experience in preclinical toxicology is... ...collaborating with other scientists and external partners...Regulatory
$178.5k - $257.83k
...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... ...pharmacology and toxicology studies, authoring regulatory documents, being a member of an...RegulatoryContract workWork experience placement$150k - $200k
...(NYSE/TSX: BLCO) is a leading global eye health company... ...cross functional Preclinical medical device expertise... ...activities, and with key regulatory expectations and... ...offices on nonclinical safety matters for country-specific... ...: ~ Ph.D. in Toxicology or related discipline...RegulatoryTemporary workRemote workWork visa- ...experienced Associate Director for Preclinical Bioanalytical Science. The role leads strategy and execution of... ...will collaborate with nonclinical toxicology, discovery biology, and clinical... ...external vendors, while contributing to regulatory documents #J-18808-Ljbffr Amylyx...Regulatory
- ...analyses focused on human health risk. You will work with scientists from toxicology, exposure science, and risk assessment on projects spanning... ...systematic reviews, weight‑of‑evidence evaluation, regulatory comment, litigation support, and producing #J-18808-Ljbffr...Regulatory
- A leading biotechnology company is seeking a Senior Scientist to join the Nonclinical Development group.... ...focuses on the nonclinical safety assessment of... ...will possess a Ph.D. in toxicology or similar field and have... ..., and contributing to regulatory submissions. The...Regulatory
$145k - $177k
Prime Medicine is a leading biotechnology company dedicated... ...self-motivated Senior Scientist to join the... ...supporting the nonclinical safety assessment function... ...will hold a Ph.D. in toxicology or a related field with... ...supporting documents for regulatory submissions....RegulatoryFull timeTemporary workFlexible hours$131.04k - $196.55k
.../Associate Director, Global Safety Scientist, MSRM Agios Pharmaceuticals... ...Sciences and the Global Safety Leads and be responsible for... ...Coordinate draft responses for regulatory authority inquiries on aggregate... ...clinical pharmacology and toxicology to interpretation of study...RegulatoryTemporary workRemote workWork from homeWorldwideFlexible hours3 days per week- ...seeking an accomplished and experienced Scientist to lead the Immune Cell Depletion Group within the... ...alongside a strong knowledge of preclinical drug discovery spanning target discovery / validation through to GLP toxicology phases. The ability to effectively collaborate...Work experience placementLocal area
- Senior Scientist, Toxicology — Cambridge, MA Our Cambridge based biotech client... ...to help shape the preclinical safety strategy for oligonucleotide... ...discovery, development, and regulatory decision‑making while... ...experience managing CROs and leading GLP/non‑GLP studies Excellent...Regulatory
- AIRNA is seeking a highly motivated Senior Scientist in Toxicology to drive pre‑clinical safety strategies for oligonucleotide programs. The role involves providing scientific leadership and serving as Study Director for toxicology studies while managing internal and external...
$157k - $213k
...disease, as well as several preclinical programs utilizing our... ...Possible", we are leading the charge toward a world... ...motivated and detail-oriented Scientist with strong expertise in... ..., discovery research, toxicology, clinical pharmacology, regulatory, and external CROs to...RegulatoryTemporary workSummer workWork at officeLocal area- ...Therapeutics in Watertown, MA seeks a seasoned Head of Toxicology to lead nonclinical safety programs, from discovery through IND and clinical development... ...GLP and non-GLP studies, partner with CROs, and guide regulatory submissions with FDA/EMA input. The role requires 10+...Regulatory
- ...Biotechnologies, based in Cambridge, MA, seeks a Senior Scientist, Pharmacology to lead in vivo pharmacology in neuroscience gene-editing programs... ..., you will also manage 1-2 research associates, prepare study reports for regulatory filings, and #J-18808-Ljbffr ArborRegulatory
$128.6k - $210k
...utilizes their scientific expertise and regulatory experience to lead nonclinical development programs with... ...and FDA/EMEA/ICH nonclinical safety guidelines to independently lead the... ...interpretation, and reporting of regulatory toxicology and/or exploratory pharmacology/...RegulatoryContract work- Aurion Biotech Inc. is seeking a Senior Scientist in Bioengineering & Therapeutics Delivery to support product development. This role... ...managing sample collections, performing analyses, and preparing regulatory documents. The position offers robust benefits and a...Regulatory
- ...Scientific Placement is seeking a Senior Scientist in Analytical Development for a Boston-... ...cancer patients. In this role, you will lead the development of analytical methods to... ...method development, project management, and regulatory compliance. This role provides a unique...Regulatory
- A pioneering biotechnology company seeks a Senior Scientist to lead the development of in vitro diagnostic products. This role involves managing research projects, ensuring compliance with regulatory standards, and mentoring junior staff. Candidates should hold a PhD in...RegulatoryWorldwide
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