Associate Director of Toxicology - Project & Regulatory
$190k - $220kVividion Therapeutics. Inc.
Vividion Therapeutics, Inc. is seeking a Project and Regulatory Toxicologist in San Diego. The role involves guiding safety assessments and overseeing toxicological studies to advance drug candidates to clinical trials. Candidates should hold a Ph.D. in pharmacology or related fields with significant industry experience. Vividion offers a competitive salary range of $190,000 to $220,000 and a comprehensive benefits package. #J-18808-Ljbffr Vividion Therapeutics. Inc.
$190k - $220k
Vividion Therapeutics, Inc. in San Diego is seeking a Project and Regulatory Toxicologist to guide safety assessments and manage toxicology studies in drug development. The ideal candidate will have a Ph.D. in pharmacology or toxicology and significant industry experience...Regulatory$190k - $220k
...size company on The San Diego Union-Tribune's 2022 to 2025 Top Workplaces list. Job Summary: The Project and Regulatory Toxicologist will be expected to use his/her toxicology expertise to guide safety assessment, design and interpret in vitro/in vivo studies to evaluate...Regulatory$155k - $193.2k
...week. Position Summary The Associate Director will oversee translational... ...preclinical safety assessment/toxicology deliverables, contributing... ...of the products, projects, and programs in support of... ...that project team goals and regulatory deliverables are met. Provide...RegulatoryWork at officeLocal areaRemote workNight shift3 days per week- A leading pharmaceutical company is seeking an Associate Director in San Diego. This role involves overseeing preclinical safety assessment and toxicology deliverables, ensuring compliance with regulatory standards. Candidates should have 8 years of relevant experience,...RegulatoryWork at office3 days per week
- ...Relocate to Australia: Associate Director - Project Architect (NSQEP) Full-time State/Province: South Australia Business Group: DCS Legal Entity... ...cohesive solutions Translate nuclear safety case and regulatory requirements into robust architectural design responses in...RegulatoryJob sharingFull timePart timeRelocationFlexible hours
- ...landscapes. From strategic planning through to project realisation, the connections we make... .... Job Description As an Associate Director - Project Architect you will lead the... ...Translate nuclear safety case and regulatory requirements into robust architectural...RegulatoryJob sharingFull timePart timeWork at officeImmediate startRemote workRelocationFlexible hours
- Associate Director, Project Management - Medical Affairs Join to apply for the Associate Director, Project Management - Medical Affairs role at... ...reviews and approvals, including scientific, MLR, regulatory, and compliance. Ensure that all medical affairs documentation...RegulatoryFull timeContract workWork at officeRemote work
$155k - $190k
...information, visit Job Summary We are seeking an experienced CMC Project Management professional to lead the planning and execution of... ...Track dependencies that could affect PPQ timing or downstream regulatory and clinical supply needs, and flag them to the CMC project...RegulatoryFlexible hours$205k - $220k
Director or Senior Director, Preclinical Pharmacology/Toxicology Viking Therapeutics is seeking an experienced and highly motivated Director or Senior Director,... ...teams, including DMPK, CMC, Clinical Pharmacology, Regulatory, and external CRO partners. The main...RegulatoryLocal area$43.17 - $62.55 per hour
...disorders. About the Role Perform day‑to‑day toxicology and safety pharmacology study contract‑... ...and keep up‑to‑date with current regulatory guidelines Other duties as assigned Requirements... ...‑functionally to ensure activities associated with toxicology and safety pharmacology...RegulatoryHourly payContract workTemporary work- ...This role is responsible for the medical review of individual case safety reports (ICSRs), ensuring data quality, consistency, and regulatory compliance. The position contributes to signal detection activities, literature review, and operational pharmacovigilance...Regulatory
- ...therapies to metastatic locations. Job Overview/Summary: The Project Manager, is a critical cross-functional role responsible for... ...Quality Control, Manufacturing Operations, Quality Assurance, Regulatory Affairs, Process Development and Analytical Development...RegulatoryFull timeContract workFlexible hours
- The Associate Director, Biologics CMC is a technical contributor responsible for supporting biologics development from upstream cell culture... ...through drug product readiness, clinical supply, and regulatory submission. This role provides technical input for large molecule...Regulatory
- ...Product Manager (Senior Staff/Associate Director Level) Hybrid on-site in San Diego, CA (no flexibility for remote work) About the Role A... ...post‑launch performance — partnering with engineering, assay, regulatory, and software teams across RUO, LDT, and IVD development phases...RegulatoryRemote work
$184k - $197k
...Associate Director, Statistical Programming Avenzo Therapeutics, Inc. ("Avenzo" or "Company... ...guidance for internal deliverables and regulatory submissions while ensuring conformance... ...changing priorities Handle multiple projects simultaneously Reasonable...RegulatoryTemporary workLocal areaRemote workHome officeMonday to ThursdayFlexible hoursNight shift$184k - $197k
...Job Title: Associate Director, Statistical Programming Location: San Diego or Remote U.S. Job... ...guidance for internal deliverables and regulatory submissions while ensuring conformance... ...frequently changing priorities Handle multiple projects simultaneously Reasonable...RegulatoryFull timeTemporary workLocal areaRemote workHome officeMonday to ThursdayFlexible hoursNight shift- ...convenience and care. POSITION SUMMARY The Associate Director, Medical Writing will provide... ...prepare high-quality complex clinical and regulatory documents for health authority submissions... ...accurate documents delivered within project timelines. Contribute towards the...RegulatoryContract work
$150k - $195k
...experienced and strategic scientist to serve as Associate Director, Bioanalytical Sciences within our... ...program objectives, timelines, and regulatory requirements. Provide strategic... ...Excellent communication, collaboration, and project leadership skills. Ability to thrive...RegulatoryTemporary workRemote work$80k - $102k
...This Job We are looking for a motivated and detail-oriented Associate Product Manager to join our Banking Fintech team. In this role... ...product initiatives that improve customer experience, ensure regulatory compliance, and support scalable growth. Responsibilities...RegulatoryWork at officeLocal area- Department: 107000 Regulatory Location: San Diego, USA - Remote Position Summary The Associate Director, Medical Writing is responsible for oversight and authoring (if needed... ...of document development strategy, overall project management during the drafting, reviewing, and...RegulatoryContract workWork at officeLocal areaRemote work
$171.8k - $235k
...treatments for tardive dyskinesia, chorea associated with Huntington's disease, classic... ...centric, AI‑enabled workflows that result in regulatory compliant data collection, analysis, and... ...reporting. This role works closely with project leads in Data Management, Statistical...Regulatory$156k - $195.6k
Position Summary The Associate Director, R&D AI Solutions & Analytics will lead the design, implementation... ...junior team members, contractors, and project contributors. Lead rapid prototyping,... ...clinical development, safety, or regulatory. Knowledge of industry data standards...RegulatoryFor contractorsWork at officeRemote workNight shift3 days per week$95k
Silver Lake Psychology is seeking an Associate Clinical Director to lead clinical supervision, training, and quality initiatives while maintaining... ...partners with leadership to ensure ethical practice, regulatory compliance, and professional development across the practice...RegulatoryRemote jobFull time$165k - $205k
...testing and sequencing. We are seeking a Associate Director of Microbiology to build and lead the... ...validation studies, in concert with Regulatory Affairs and Assay Development, that meet... ...support across multiple concurrent projects. Build the scalable microbiology workflows...RegulatoryInterim roleLocal areaImmediate start$172k - $258k
...are seeking a dynamic and experienced Associate Director of Laboratory Engineering and Technology... ...that laboratory operations align with regulatory standards while leveraging digital... ...Execute strategic plans for assigned projects or functions, ensuring alignment with...RegulatorySummer workLocal areaRemote workFlexible hours2 days per week$200k - $265k
Associate Director/Director, Medical Affairs Strategy About Soleno Therapeutics Inc Soleno is a biopharmaceutical company focused on the development... ...and external stakeholders. In‑depth knowledge of the regulatory environment and compliance requirements related to medical...Regulatory$155k - $190k
...Job Title: Associate Director, Clinical Data Systems and Informatics Location: San Mateo, CA;... ...CDM documentation in accordance with regulatory inspection readiness standards Coordinate... ...data with other corporate data Provide project status updates to cross‑functional...Regulatory- ...collaborating to bring new therapies to patients in need. Position The Associate Director/ Director of Drug Safety & Pharmacovigilance (PV) Quality &... ...processes and systems to ensure compliance/alignment with regulatory requirements and internal policies/procedures. Proactively...Regulatory
$161k - $180k
...Associate Director, Quality Assurance Avenzo Therapeutics, Inc. ("Avenzo" or "Company") is... ...Reporting to the Senior Vice President, Regulatory Affairs the Associate Director, Quality... ...priorities Handle multiple projects simultaneously Reasonable accommodations...RegulatoryContract workTemporary workWork at officeLocal areaRemote workHome officeMonday to ThursdayFlexible hoursNight shift- Travere Therapeutics is looking for an Associate Director of Analytical Development based in San Diego, California. This role involves leading... ...with external labs, and ensuring compliance with regulatory standards. The ideal candidate has over 8 years of experience...RegulatoryRemote job
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