Associate Director, Toxicology
$171k - $223kScorpion Therapeutics
Neurodegenerative diseases are one of the largest medical challenges of our time. Denali Therapeutics is a biotechnology company dedicated to developing breakthrough therapies for neurodegenerative diseases through our deep commitment to degeneration biology and principles of translational medicine. Denali is founded on the collaboration of leading scientists, industry experts, and investors who share the vision that scientific discovery energetically applied to translational medicine is the key to delivering effective therapies to patients. We invite you to consider an opportunity with Denali to help achieve our goal of delivering meaningful therapeutics to patients. Leads nonclinical safety strategy for development programs, advancing assets from discovery through clinical stages. Shapes toxicology approaches, interprets complex data, and influences program decisions to ensure patient safety and regulatory success. Serves as a scientific authority in toxicology, integrating cross‑functional insights and external regulatory expectations. Drives innovation in safety assessment while contributing to organizational scientific leadership. Key Accountabilities / Core Job Responsibilities Develop and lead nonclinical toxicology strategies for multiple programs across discovery and development stages Interpret toxicology and safety pharmacology data to inform risk assessment and program decisions Provide strategic input into regulatory submissions, including IND‑enabling studies and health authority interactions Influence cross‑functional teams by integrating toxicology insights with clinical, regulatory, and translational considerations Oversee design, execution, and interpretation of outsourced and internal toxicology studies Identify and mitigate safety risks, proposing alternative strategies to advance programs Contribute to governance discussions, representing toxicology perspectives in decision‑making forums Build external scientific network and monitor emerging trends in toxicology and safety sciences Mentor junior scientists and provide scientific guidance across the organization Drive continuous improvement of toxicology processes, tools, and scientific approaches Qualifications / Skills Typically PhD in Toxicology, Pharmacology, or related life sciences field with 10+ years of relevant industry experience or relevant combination of education and experience Demonstrated expertise in nonclinical safety assessment across multiple therapeutic modalities or indications Proven ability to lead toxicology strategy for programs advancing into clinical development Experience supporting regulatory submissions and interacting with health authorities preferred Strong scientific judgment with the ability to interpret complex and ambiguous data sets Ability to influence cross‑functional teams without direct authority Effective communication skills, including the ability to translate technical findings into business and clinical implications Salary Range: $171,000.00 to $223,000.00. Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience. Denali offers a competitive total rewards package, which includes a 401k, healthcare coverage, ESPP and a broad range of other benefits. Learn more at This compensation and benefits information is based on Denali’s good faith estimate as of the date of publication and may be modified in the future. Denali is committed to its core company value of unity by creating a diverse and inclusive environment. We are proud to be an equal opportunity employer and do not discriminate against any employee or applicant for employment because of race, color, sex, age, national origin, religion, sexual orientation, gender identity and/or expression, status as a veteran, basis of disability, or any other federal, state, or local protected class. #J-18808-Ljbffr
$155k - $193.2k
...work in our office three days per week on average. Position Summary The Associate Director will be responsible for the oversight of Translational Science preclinical safety assessment/toxicology deliverables, with a clear understanding of functional interdependence and...SuggestedWork at officeLocal areaRemote workNight shift3 days per week$171k - $223k
...Associate Director, ToxicologySkip to main content#Associate Director, Toxicology page is loaded## Associate Director, ToxicologyApplylocations: South San Franciscotime type: Full timeposted on: Posted 10 Days Agojob requisition id: R-1560Neurodegenerative diseases are...SuggestedLocal area$195k - $215k
...treating patients in a phase 1 trial. We are looking for an Associate Director or Director of Protein Sciences to lead protein sciences and... ...meeting in‑vivo dosing specifications for pharmacology and toxicology studies. Analytical & Developability Characterization Manage...Suggested- Acadia Pharmaceuticals Inc. in South San Francisco is looking for an Associate Director to oversee preclinical safety assessment and toxicology deliverables. This role requires collaboration on various projects, ensuring effective communication among teams, and managing...Suggested
- ...We are seeking a highly motivated and experienced Associate Director of Toxicology (Nonclinical Safety) to support the advancement of our pipeline programs. This individual will play a key role in designing, executing, and interpreting nonclinical safety strategies across...Suggested
- ...Associate Director Clinical Pharmacology – San Francisco Biotech New Position: Associate Director Clinical Pharmacology – San Francisco Biotech... ..., clinical operations, drug metabolism, biology/biomarkers, toxicology etc. Provide clinical pharmacology expertise in the...
- Latigo Biotherapeutics, Inc. is seeking an experienced Associate Director of Toxicology in San Francisco, California. This role involves designing, overseeing, and interpreting nonclinical safety strategies essential for pipeline progression. The ideal candidate will have...
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...high unmet need, including cardiovascular, metabolic, and pulmonary conditions. Position Summary This role will report to the Sr. Director Program Management. It is the execution engine of the late‑stage clinical program, managing overall project timelines, risks, and...Work experience placementOverseasAfternoon shift2 days per week1 day per week- Associate Director - Computational Biology (Cardiovascular, Metabolic, Obesity and Related) We are looking for an experienced Computational Biologist with expertise in analyzing clinical biomarker data such as metabolomics, genomics, transcriptomics, proteomics, spatial...Flexible hours
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Amgen is seeking an Associate Director - Computational Biology to lead the analysis of clinical biomarker data in South San Francisco. The successful candidate will integrate computational biology techniques with biological and clinical data to drive evidence generation...- Amgen’s Computational Biology group within the Center for Technology and Innovation (CfTI) is seeking a highly motivated Computational Biologist to analyze clinical biomarker data across metabolomics, genomics, transcriptomics, proteomics, spatial‑omics, flow cytometry,...
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ASSOCIATE DIRECTOR, BIOCONJUGATION Sutro Biopharma is seeking an innovative and highly motivated Associate Director to join the Protein Biochemistry Group. The successful candidate will serve as a scientific leader in bioconjugation and analytical characterization of conjugates...$156k - $195.6k
...Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average. Position Summary The Associate Director, R&D AI Solutions & Analytics will serve as a strategic and technical leader responsible for advancing AI-enabled analytics...For contractorsWork at officeLocal areaRemote workNight shift3 days per week- Xaira Therapeutics in South San Francisco is looking for an Associate Director in Analytical Development (Biologics) to lead and oversee analytical strategies for biologics programs through clinical execution. You will be responsible for method development, validation,...Flexible hours
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Sutro Biopharma is looking for an innovative Associate Director to join its Protein Biochemistry Group in South San Francisco. The ideal candidate will lead bioconjugation efforts for antibody-drug conjugates (ADCs) and drive innovation in conjugation chemistry. Applicants...- Sutro Biopharma, Inc. is seeking an innovative Associate Director to join the Protein Biochemistry Group in South San Francisco. The successful candidate will serve as a scientific leader in bioconjugation, driving the development of next-generation antibody-drug conjugates...
$215k - $265k
...and exciting place to catalyze and enable medical breakthroughs. Position Description Calico is seeking a highly motivated Associate Director/Director to join our Translational Medicine team. The successful candidate will lead our preclinical in vivo physiology efforts...$186k - $235k
...chronic diseases with high unmet need, including cardiovascular, metabolic, and pulmonary conditions. Position Summary The Associate Director of Medical Writing will be responsible for leading the development of key regulatory and clinical documents supporting the company...Remote work$154k - $300k
Analytical Characterizations October 2025 Department: Technology Position Summary: Soleil is seeking an expert and engaged Associate Director / Director , Analytical Lead to head our analytical and biophysical characterization efforts within the Protein Sciences group...Temporary workFlexible hours$182.47k - $246.87k
...within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career. Associate Director - Computational Biology (Cardiovascular, Metabolic, Obesity and Related) What you will do Let’s do this. Let’s change the...Flexible hours$230k - $240k
...create an inspiring and exciting place to catalyze and enable medical breakthroughs. Position Description Calico is seeking an Associate Director, Medical Writing to provide leadership and functional oversight for writing and leading the review/approval process of high...For contractorsWork at office- We are seeking an Associate Director, Medical Writing to lead the development and execution of high-quality clinical and regulatory documentation. This individual will play a key role in shaping document strategy, managing the end-to-end writing process, and ensuring compliance...Contract workWork at office
$137.5k - $261k
...priorities across the organization. The work of this team plays a vital role in shaping AbbVie's continued growth and success. The Associate Director of AI Transformation will support major change initiatives and drive organizational transformation to enable AbbVie’s...Temporary work$210k - $260k
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