Top 136 Associate Director Toxicology Jobs

Associate Director, Toxicology
Protagonist Therapeutics —Newark, CA
- $185,000 - $205,000 a year
- Project management
- Doctor of Philosophy
- Pediatrics
Quick Apply
Associate Director, Toxicology
Denali Therapeutics —South San Francisco, CA
- $171,000 - $223,000 a year
- Doctor of Philosophy
- Mentoring
- Senior level
- Employee stock purchase plan
- Health insurance
Director / Associate Director – Toxicology
Monte Rosa Therapeutics, Inc —Boston, MA
- $185,000 - $260,000 a year
- Full-time
- 5 years
- Master's degree
- Doctor of Philosophy
Associate Director Toxicology
GlaxoSmithKline —Upper Providence, PA
- Full-time
- 5 years
- Bachelor's degree
- Doctor of Philosophy
Associate Director Toxicology
Acadia Pharmaceuticals Inc. —San Diego, CA
- $155,000 - $193,200 a year
- Hybrid work
- 6 years
- Bachelor of Science
- Office
- Paid parental leave
- Employee stock purchase plan
Associate Director, Toxicology
Ionis Pharmaceuticals, Inc. —Carlsbad, CA
- $172,501 - $255,000 a year
- Hybrid work
- Master's degree
- Doctor of Philosophy
- In-person
Quick Apply
Associate Director, Discovery Pharmacology
Amylyx Pharmaceuticals —Cambridge, MA
- $186,000 - $209,000 a year
- Master's degree
- Bachelor's degree
- Doctor of Philosophy
10d
Associate Director, Project and Regulatory Toxicologist
Vividion Therapeutics, Inc —San Diego, CA
- $190,000 - $220,000 a year
- 6 years
- Doctor of Philosophy
- Quality control
- Disability insurance
- Health insurance
Quick Apply
Emergency Medicine Residency Program Director
Physician Affiliate Group of New York —Bronx, NY
- $352,500 a year
- Full-time
- Medicine
- BC/BE
- Mentoring
- AD&D insurance
- Health insurance
Quick Apply
Emergency Medicine Residency Program Director
Physician Affiliate Group of New York —Bronx, NY
- $352,500 a year
- Full-time
- Medicine
- BC/BE
- Mentoring
- AD&D insurance
- Health insurance
Quick Apply
Health Home RN Care Manager
Arundel Lodge, Inc. —Edgewater, MD
- $30 - $32 an hour
- Overtime
- Nursing
- Vital signs
- RN License
Quick Apply
Technical Coordinator
Sonora Quest Laboratories —Phoenix, AZ
- Night shift
- Customer service
- Computer literacy
- Writing skills
13d
Pathologists' Assistant
Hartford Pathology Associates —Norwich, CT
- Full-time
- Background check
- Surgery
- OSHA
- Profit sharing
- Continuing education credits
Quick Apply
Laboratory Technical Coordinator - Banner Boswell (Day Shift)
Sonora Quest Laboratories —Sun City, AZ
- From $33.33 an hour
- Day shift
- Customer service
- Mid-level
- Associate's degree
LAB Technical Coordinator I
Sonora Quest Laboratories —Loveland, CO
- $33.33 - $55.56 an hour
- Full-time
- Hospital
- Customer service
- Mid-level
Technical Coordinator (Chemistry) - Banner Estrella (Day Shift)
Sonora Quest Laboratories —Phoenix, AZ
- From $33.33 an hour
- Day shift
- Customer service
- Mid-level
- Associate's degree
13d
Service Coordinator
Acacia Network —Bronx, NY
- $24.72 an hour
- Full-time
- Pass drug screening
- Mid-level
- Apartments
- Paid holidays
- Health insurance
Quick Apply
Associate Director Clinical Pharmacology and Pharmacokinetics
Viking Therapeutics, Inc. —San Diego, CA
- $140,000 - $185,000 a year
- 6 years
- Bachelor of Science
- Writing skills
Quick Apply
Research Associate I - In Vitro
Biolegacy Research —San Diego, CA
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Bachelor's degree
Quick Apply
Associate Scientist
Frontage Laboratories —Exton, PA
- Full-time
- Research
- Mid-level
- Master's degree
- Disability insurance
- Health insurance
Quick Apply

I want to receive the latest job alert for Associate Director Toxicology

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

Associate Director Toxicology jobs near

Service Coordinator jobs in Bronx, NY

Associate Director jobs in San Diego, CA

Associate Director jobs in Cambridge, MA

Technical Coordinator jobs in Phoenix, AZ

Associate Director jobs in Boston, MA

Research Associate jobs in San Diego, CA

Toxicologist jobs in San Diego, CA

Associate Director jobs in South San Francisco, CA

Work From Home Customer Service jobs in Connecticut

Clinical Research Coordinator jobs in Berkeley, CA

Service Coordinator jobs in Cleveland, OH

Service Coordinator jobs in Oak Lawn, IL

Operations Coordinator jobs in Boston, MA

Service Coordinator jobs in Illinois

Service Coordinator jobs in Louisiana

Associate Director jobs in Wilmington, DE

Associate Director jobs in Riverside, CA

Activity Director jobs in San Antonio, TX

Associate Director jobs in Fort Myers, FL

Mental Health Associate No Experience jobs in New Jersey

Associate Director, Toxicology

Protagonist Therapeutics -
Newark, CA

Quick Apply

Job Details

$185,000 - $205,000 a year

Qualifications

Team supervision
GxP
Pre-clinical study projects
Data-driven problem-solving
Research data analysis
Budgeting
Cross-functional collaboration
Pharmaceutical research experience
Cross-functional communication
Toxicology research projects

Full Job Description

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). This role will lead and manage CRO and consultant activities that support drug research and development across the PTGX pipeline. The successful candidate will be responsible for developing nonclinical toxicology strategies, overseeing GLP and non-GLP studies, preparing toxicology components of regulatory submissions, and responding to inquiries from regulatory authorities. This position will report to the Senior Vice President, Toxicology, Nonclinical Development.

Responsibilities:

Serve as a self-directed toxicology leader and key member of a dynamic team supporting PTGX drug discovery and development programs.

Independently develop phase-appropriate nonclinical toxicology strategies for PTGX pipeline molecules and represent toxicology on cross-functional project teams.
Design, revise, and finalize nonclinical toxicology study protocols, study designs, data analyses, and reports, including plans that support first-in-human and later-stage clinical development.
Prepare and critically review nonclinical toxicology sections for IND, CTA, NDA, and other regulatory submissions, ensuring alignment with applicable US and ex-US regulatory expectations.
Identify, evaluate, and resolve program-specific toxicology issues in collaboration with the supervisor, project teams, CROs, consultants, and other subject-matter experts.
Critically review and edit CRO nonclinical toxicology and related study reports, including pharmacology, ADME, PK/TK, safety pharmacology, and pathology reports; analyze and interpret data; and coordinate report finalization.
Ensure study documentation and regulatory deliverables are scientifically sound, timely, and consistent with global regulatory and compliance requirements.
Manage and monitor GLP and non-GLP nonclinical studies conducted at CROs in accordance with PTGX vendor management SOPs and policies, ensuring quality, timelines, and regulatory compliance are met or exceeded.
Provide clear analysis, interpretation, and visualization of nonclinical toxicology and related data for internal communications, program team presentations, regulatory interactions, and decision-making.
Maintain current knowledge of relevant scientific literature, methodologies, regulatory guidance, and emerging best practices applicable to PTGX pipeline products and nonclinical development programs.

Qualifications:

PhD or DVM in biological sciences, toxicology, pharmacology, or a related discipline.
DABT board certification is preferred.
Minimum of 5–10 years of relevant drug development experience, preferably in the biotechnology or pharmaceutical industry.
Demonstrated experience developing and executing nonclinical toxicology strategies that support IND-enabling studies, first-in-human clinical trials, and later-stage development programs.
Strong working knowledge of Good Laboratory Practice regulations and relevant FDA, ICH, OECD, EMA, and other global nonclinical safety guidelines.
Experience in preclinical development, toxicology, nonclinical pharmacology, drug metabolism, pharmacokinetics, and toxicokinetics.
Proven ability to manage CROs, consultants, and external academic or industry collaborators, including oversight of study design, budgets, timelines, monitoring, data review, and final reports.
Broad and integrated understanding of pharmacology, toxicology, DMPK, safety pharmacology, pathology, and translational safety assessment.
Excellent verbal and written communication skills, with the ability to build strong working relationships with internal colleagues, cross-functional teams, external vendors, and consultants.
Strong scientific background, preferably demonstrated through peer-reviewed publications, regulatory writing experience, or presentations in relevant medical and life science forums.
Excellent decision-making, complex problem-solving, critical thinking, data analysis, and data interpretation skills.
Highly motivated, flexible, and proactive self-starter who takes ownership of new tasks and delivers high-quality results with limited supervision.
Demonstrated ability to be productive and successful in a fast-paced, matrixed, and multi-tasking work environment.

The base pay range for this position at commencement of employment is expected to be between $185K and $205K / year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.

Protagonist Therapeutics is a discovery through late-stage development biopharmaceutical company. The Company's proprietary peptide technology platform enables de novo discovery of peptide therapeutics. Two novel peptides derived from Protagonist's proprietary discovery platform are at or near commercialization. ICOTYDE™ (icotrokinra) is approved in the U.S. for the treatment of moderate-to-severe plaque psoriasis in adults and pediatric patients 12 years of age and older who weigh at least 40 kg who are candidates for systemic therapy or phototherapy. ICOTYDE is the first and only targeted oral peptide that precisely blocks the Interleukin-23 receptor (IL-23R) licensed to Janssen Biotech, Inc.,a Johnson & Johnson company. ICOTYDE was jointly discovered by Protagonist and Johnson & Johnson scientists, with Protagonist having primary responsibility for the development of ICOTYDE through Phase 1, and Johnson & Johnson assuming responsibility for further development and commercialization. An NDA for rusfertide, a first-in-class hepcidin mimetic peptide that is being co-developed with Takeda Pharmaceuticals pursuant to a worldwide license and collaboration agreement entered in 2024, is under priority review with the FDA. Protagonist holds an option to co-commercialize rusfertide in the U.S. through a 50/50 profit and loss share structure or can opt-out of this structure. 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.

More information on Protagonist, its pipeline drug candidates, and clinical studies can be found on the Company's website at https://www.protagonist-inc.com.

Quick Apply

Refine Your Search

Associate Director Toxicology jobs

Associate Director, Toxicology

Associate Director, Toxicology

Director / Associate Director – Toxicology

Associate Director Toxicology

Associate Director Toxicology

Associate Director, Toxicology

Associate Director, Discovery Pharmacology

Associate Director, Project and Regulatory Toxicologist

Emergency Medicine Residency Program Director

Emergency Medicine Residency Program Director

Health Home RN Care Manager

Technical Coordinator

Pathologists' Assistant

Laboratory Technical Coordinator - Banner Boswell (Day Shift)

LAB Technical Coordinator I

Technical Coordinator (Chemistry) - Banner Estrella (Day Shift)

Service Coordinator

Associate Director Clinical Pharmacology and Pharmacokinetics

Research Associate I - In Vitro

Associate Scientist

I want to receive the latest job alert for Associate Director Toxicology

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected