41 Results for

Toxicology Jobs in Kenmore, MA

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Research Leader (Toxicology), Cambridge, MA Isomorphic Labs

Cambridge, MA

If you are an experienced, innovative and ambitious scientist looking to play an active part in the AI-driven transformation of the pharmaceutical industry, joining Isomorphic Labs will lift you out of your comfort zone and provide an amazing opportunity for personal growth and development. Since Isomorphic Labs outsource all wet-lab work to external vendors, you will maintain and develop close relationships with the CRO network to: Ensure high quality and timely data generation to support our portfolio projects.

30+ days ago

Director, Study Quality and Compliance - Nonclinical Safety/Toxicology Novartis AG

Cambridge, MA

$185,500–$344,500 / year

Key Responsibilities: Lead and provide strategic oversight to the PCS Study Quality and Compliance team including responsibility for establishing long-term strategy and yearly goals which support itModernize the group functionality leading the implementation of tracking, management, and data analytics software (eg, Smartsheet) across the toxicology line function to enhance quality and compliance oversight of toxicology studiesOversight of toxicology study data management from external and internal studies; this includes data suitability and availability for our internal toxicology study data warehouseOversight and responsibility for ensuring SEND datasets are of high-quality and are ready in a timely manner for regulatory submissions, which includes SEND datasets from external CRO and de novo generation for internal non-GLP studiesOversight of SOPs and training records for PCS personnel to ensure compliance with GLP expectations, and serve as the management interface with the Archive Records Management teamOversight of support for biomarker and pathology with respect to shipment of study samples and data transfer of digital slidesSupport diligence acquisition and licensing deals through oversight and management of study-related data (including SEND) that need to be transferred Essential Requirements: Advanced degree in biological-related sciences with at least 10 years of relevant pharmaceutical experience, BS degree in biological-related science with at least 15 years of experience, or 25+ years of relevant industry experience in oversight and compliance of toxicology studies. Previous experience working with GLP guidelines and pharmaceutical toxicology studies, and associated quality, compliance, and animal welfare attributesPrevious experience with software tools for data and/or program management is highly desiredPrevious experience with SEND, or at a minimum good general familiarity with its requirements is desiredGood communication skills, and excellent logistical/planning skillsFluent in English (spoken and written)The salary for this position is expected to range between: $185,500 and $344,500 per year.

8 days ago

Vice President, Nonclinical Drug Safety & Toxicology Remix Therapeutics Inc

Watertown, MA

$293,000–$358,000 / year

The Non-Clinical Safety and Toxicology leader will partner cross-functionally across therapeutic areas with colleagues in drug discovery, translational, and clinical development functions, ensuring toxicology and nonclinical safety data is shared and communicated transparently and plays a role in informing strategy at all stages of each program's development. Position Summary: Reporting to the Chief Scientific Officer, the Vice President of Nonclinical Drug Safety and Toxicology is a key position within the R&D leadership team and will lead nonclinical aspects of all the company's pipeline programs.

30+ days ago

Senior Director, Toxicology Stoke Therapeutics, Inc.

Bedford, MA

$285,000–$320,000 / year

The successful candidate will play a key role at Stoke Therapeutics leading the nonclinical toxicology work in support of our drug discovery and clinical programs and will have hands-on responsibility for preparation of preclinical safety data packages for clinical development and product registration. Key Responsibilities: Provide leadership, technical oversight, and guidance for all nonclinical safety studies conducted to support Stoke Therapeutics discovery and development programs to ensure delivery of a high-quality safety package for development and registration.

30+ days ago

Senior Advisor, Study Operations Manager - Nonclinical Toxicology Centessa Pharmaceuticals Plc

Boston, MA

$150,000–$220,000 / year

Centessa Pharmaceuticals is seeking an experienced Senior Advisor, Study Operations Manager - Nonclinical Toxicology who will operate at the Associate Director level to manage and oversee day-to-day operations for toxicology and safety pharmacology studies conducted in the selected CROs to include study forecasting, budgeting, planning, data management, quality assurance, compliance, communications and collaboration with different functional teams across the portfolio of Orexin agonist programs. Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company, is a clinical-stage company developing orexin receptor 2 (OX2R) agonists as a new class of medicines for the treatment of narcolepsy and potentially other sleep-wake disorders.

30+ days ago

Vice President/Senior Director, Nonclinical Drug Safety & Toxicology Remix Therapeutics

Watertown, MA

$293,000–$358,000 / year

The Non-Clinical Safety and Toxicology leader will partner cross-functionally across therapeutic areas with colleagues in drug discovery, translational, and clinical development functions, ensuring toxicology and nonclinical safety data is shared and communicated transparently and plays a role in informing strategy at all stages of each program’s development. Reporting to the Chief Scientific Officer, the Vice President/Senior Director of Nonclinical Drug Safety and Toxicology is a key position within the R&D leadership team and will lead nonclinical aspects of all the company’s pipeline programs.

16 days ago

Senior Director, Toxicology Amylyx Pharmaceuticals

Cambridge, MA

Remote

$269,000–$291,667 / year

Develop and execute comprehensive nonclinical safety strategies to support clinical candidate selection, IND-enabling activities, regulatory submissions, and clinical development across multiple programs including small molecules, peptides, protein-based biologics, anti-sense oligonucleotides. This person will: Serve as a toxicology leader across a diverse and expanding pipeline spanning multiple therapeutic areas and drug modalities, shaping nonclinical safety strategy from discovery to IND-enabling and throughout clinical phases.

30+ days ago

Associate Director, Toxicology (Nonclinical Safety Evaluation) City Therapeutics

Cambridge, Massachusetts

PhD or DVM, or equivalent advanced degree in Toxicology, Pharmacology, Pathology, Veterinary Sciences, or a related field, with 5+ years, Masters with 7+ or a Bachelors with 10+ of relevant experience in biotech or pharmaceutical drug development, or direct experience as a Study Director at a GLP-qualified CRO. We’re seeking an Associate Director, Nonclinical Safety Evaluation (NSE) who will play a pivotal role in overseeing and critically evaluating nonclinical safety studies across City’s RNAi therapeutic programs.

30+ days ago

Senior Director, Toxicology Amylyx Pharmaceuticals Inc

Cambridge, MA

Remote

$269,000–$291,667 / year

30+ days ago

Research Leader Toxicology, Cambridge, MA Isomorphic Labs Limited

Cambridge, MA

30+ days ago

Nonclinical Toxicology Study Monitoring Scientist Vertex Pharmaceuticals Inc

Boston, MA

Remote

$101,600–$152,400 / year

This role is best suited for a scientifically grounded, highly organized, collaborative study monitor who thrives in a fast-paced environment, excels at managing multiple studies and competing priorities simultaneously, and communicates clearly and succinctly to drive study execution and decision-making. We are seeking a Nonclinical Toxicology Study Monitoring Scientist to play a critical role in supporting the safety assessment of both large and small molecule modalities including cell and gene therapies across the development pipeline by providing scientific, technical, and operational oversight of outsourced nonclinical studies.

30+ days ago

Director/Senior Director, Nonclinical Safety (Toxicology) Nimbus Therapeutics

Boston, MA

$225,000–$285,000 / year

Manage nonclinical safety studies conducted by CROs with efficient governance including contract execution, authorization of study amendments, schedule and budget variance management, progress reporting to stakeholders, review of data and draft study reports, completion of contract milestones, study close-out and alignment of nonclinical safety evaluations with drug development efforts and priorities. Collaborate with CMC, Program & Portfolio Management, Clinical, Medical, and Regulatory Affairs to develop program-specific strategies for appropriate data generation in support of development candidate nomination, IND/CTA filing, and clinical development of new small molecule drug entities.

30+ days ago

Senior Director, Toxicology Disc Medicine Inc

massachusetts, MA

$261,000–$319,000 / year

Reporting directly to the Vice President, Head of Toxicology, the successful candidate will play a pivotal role in leading nonclinical safety assessments and driving toxicology strategy across the Disc portfolio. The ideal candidate will also blend deep technical knowledge in nonclinical safety and pharmacokinetics with strong communication skills to cross-functionally guide programs toward clinical success.

30+ days ago

Senior Advisor, Study Operations Manager - Nonclinical Toxicology Centessa Pharmaceuticals, LLC

Boston, MA

$150,000–$220,000 / year

13 days ago

Director, Toxicology Enanta Pharmaceuticals

Watertown, MA

$173,000–$250,000 / year

Strong communication and cross-functional influencing skills, including the ability to clarify needs, influence decisions using data and logic, navigate ambiguity, resolve conflicts constructively, and communicate complex scientific data to senior leadership and regulatory authorities. Enanta’s clinical programs are currently focused on respiratory syncytial virus (RSV) and its earlier-stage immunology pipeline aims to develop treatments for inflammatory diseases by targeting key drivers of the type 2 immune response, including KIT, STAT6 and MRGPRX2 inhibition.

14 days ago

Senior Director, Toxicology Alnylam Pharmaceuticals Inc

Cambridge, MA

$222,800–$314,000 / year

Excellent written, verbal, and presentation skills, with the ability to communicate complex scientific and regulatory topics clearly to project teams, senior leaders, external partners, and regulatory authorities. This role shapes nonclinical development strategy within or across therapeutic areas and provides scientific oversight for the design, conduct, interpretation, and reporting of GLP and non-GLP toxicology studies conducted at contract research organizations.

13 days ago

Associate Director, Toxicology Parabilis Medicines

Cambridge, MA

$170,000–$210,000 / year

Parabilis Medicines is seeking a highly motivated and driven Associate Director, Toxicology to lead nonclinical safety programs across a diverse pipeline built on Parabilis' clinically validated Helicon pipeline. The successful candidate will serve as the nonclinical safety lead on cross-functional project teams, working autonomously to define strategy, drive execution, influence candidate selection, and ensure robust safety assessment across our pipeline.

30+ days ago

Senior Scientist, Safety Assessment and Investigative Toxicology Eli Lilly and Co

Boston, MA

$66,000–$189,200 / year

Advanced Data Visualization & Analytics: Lead the architectural design and execution of data models that transform raw, multi-dose toxicology data streams, clinical pathology tables, and safety pharmacology metrics into publication-ready visual tools (e.g., exposure-margin heatmaps, benchmark dose plots, and cumulative trend diagnostics) to clearly define therapeutic windows. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).

2 days ago

ViiV Healthcare (GSK) Director/Toxicology Project Specialist GSK plc

Boston, MA

$162,000–$270,000 / year

Biotechnology, Business Strategies, Cell Biology, Cross-Functional Teamwork, Drug Development, Drug Discovery Process, Influencing Without Authority, Interpersonal Communication, Life Science, Market Opportunities, Matrix Leadership, Molecular Biology, Scientific Research, Scientific Writing, Strategic Alignment. You will work in a highly matrixed global environment and collaborate extensively to evolve non-clinical safety strategies based on input from market research, competitive intelligence, and learnings from internal programs.

30+ days ago

Director, Nonclinical Development - Toxicology Rhythm Pharmaceuticals

Boston, MA

$182,000–$275,000 / year

This individual will serve as the toxicology subject matter expert and will be accountable for driving integrated, cross‑functional nonclinical development strategies and workstreams — leading the design, interpretation, and regulatory positioning of safety assessment programs supporting small molecule and peptide therapeutics from IND‑enabling studies through late‑stage development and registration. The Director will be expected to distill complex scientific and technical information into clear, actionable messages and to communicate strategic priorities, data interpretation, and risk cross‑functionally and to senior leadership with clarity and confidence.

28 days ago

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Toxicology Jobs in Kenmore, MA

Research Leader (Toxicology), Cambridge, MA Isomorphic Labs

Director, Study Quality and Compliance - Nonclinical Safety/Toxicology Novartis AG

Vice President, Nonclinical Drug Safety & Toxicology Remix Therapeutics Inc

Senior Director, Toxicology Stoke Therapeutics, Inc.

Senior Advisor, Study Operations Manager - Nonclinical Toxicology Centessa Pharmaceuticals Plc

Vice President/Senior Director, Nonclinical Drug Safety & Toxicology Remix Therapeutics

Senior Director, Toxicology Amylyx Pharmaceuticals

Associate Director, Toxicology (Nonclinical Safety Evaluation) City Therapeutics

Senior Director, Toxicology Amylyx Pharmaceuticals Inc

Research Leader Toxicology, Cambridge, MA Isomorphic Labs Limited

Nonclinical Toxicology Study Monitoring Scientist Vertex Pharmaceuticals Inc

Director/Senior Director, Nonclinical Safety (Toxicology) Nimbus Therapeutics

Senior Director, Toxicology Disc Medicine Inc

Senior Advisor, Study Operations Manager - Nonclinical Toxicology Centessa Pharmaceuticals, LLC

Director, Toxicology Enanta Pharmaceuticals

Senior Director, Toxicology Alnylam Pharmaceuticals Inc

Associate Director, Toxicology Parabilis Medicines

Senior Scientist, Safety Assessment and Investigative Toxicology Eli Lilly and Co

ViiV Healthcare (GSK) Director/Toxicology Project Specialist GSK plc

Director, Nonclinical Development - Toxicology Rhythm Pharmaceuticals

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