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Director, Nonclinical Development
Boston, Massachusetts, United States
$182k-$275k/yr HybridFull Time
10+ YOEPhD, DVM, or equivalent in Toxicology/Pharmacology; 10+ years nonclinical development experience; strong toxicology, DMPK, ADME; IND-enabling and regulatory package delivery; CRO management; strong communication and regulatory document contribution.
GLP, IND, DMPK, ADME, CRO management, Regulatory documentation
2w
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Senior Director Nonclinical Development
United States
$151k-$314k/yr RemoteFull Time
15+ YOEBachelor's degree and ~15 years' experience in pharmaceutical nonclinical development; expert knowledge of regulatory submissions, GMP/GLP/GCP, strong communication and supervisory skills.
4w
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Associate Director / Director, Nonclinical Regulatory Affairs
Paramus, New Jersey, United States
$170k-$200k/yr HybridFull Time
10+ YOESenior nonclinical regulatory lead for FDA and EMA interactions; strong nonclinical safety/toxicology background, GLP knowledge, experience with IND/NDA/BLA and briefing documents; PhD/MD/DVM or equivalent and typically 10+ years in nonclinical drug development.
2mo
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Vice President, Head, Nonclinical Development
South San Francisco, California, United States
$235k-$256k/yr HybridFull Time
10+ YOE5+ MgmtPhD in toxicology or pharmacology; 10+ years drug development; 5+ years leadership; experience with nonclinical safety, PK/PD/ADME; CRO/vendor management; regulatory interactions.
Toxicology, Pharmacology, PK/PD, ADME, Bioanalytical methods, GLP, GMP, Regulatory documentation
1mo
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AIRx, Sr. Director, Nonclinical Safety Lead
Cambridge or Boston
$212k-$333k/yr HybridFull Time
12+ YOEPhD-level toxicology expert with 12+ years in nonclinical safety and IND-enabling toxicology; board certification preferred; experience designing and directing CRO GLP and non-GLP studies, regulatory knowledge (ICH/FDA/EMA), and AI/ML data literacy.
TetraScience, SAIL, AI/ML
2mo
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Fellow, Nonclinical Sciences
United States
RemoteFull Time
10+ YOEPhD in Pharmacology/Toxicology or related field; 10+ years in pharmacology/toxicology; regulatory knowledge; strong analytical, problem-solving, and communication skills.
1mo
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Associate Director, Nonclinical Safety Evaluation
Cambridge, Massachusetts, United States
$174k-$196k/yr OnsiteFull Time
7+ YOEPhD, DVM or equivalent in Toxicology/Pharmacology/Pathology/Veterinary Sciences; 7+ years biotech/pharma experience; GLP/N-GLP study oversight; CRO collaboration; strong data interpretation.
GLP, Nonclinical Safety, Toxicology, Study Design, Regulatory Submissions, CRO Management
1w
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Regulatory Affairs Consultant – Nonclinical Cell & Gene Therapy
United States
$95k-$116k/yr RemoteFull Time
2+ YOEAdvanced degree in relevant life-science field, 2+ years nonclinical/regulatory experience, strong scientific writing and regulatory knowledge, ability to support nonclinical strategies for cell and gene therapies.
1w
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Principal Medical Writer-nonclinical focus
Massachusetts or United States or Canada
$132k-$151k/yr RemoteFull Time
7+ YOEBachelor's required (MS/PhD preferred),7+ years regulatory/nonclinical writing experience (CTD Module 2.4/2.6),ability to lead project teams,prepare submission-level documents,proficiency with Microsoft Word.
Microsoft Word
2mo
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Director, Nonclinical Due Diligence & External Innovation
Glattbrugg or Waltham
HybridFull Time
10+ YOESenior-level director with 10+ years nonclinical development, due diligence, and external innovation experience; strong cross-functional leadership and communication.
1w
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VP, Translational Science (Nonclinical) Development
Berkeley Heights or Frederick
$285k-$380k/yr OnsiteFull Time
15+ YOE5+ MgmtDoctoral degree required; 15+ years pharma/biotech R&D experience with 5+ years leadership; expertise in translational science, nonclinical development, IND-enabling studies, regulatory interactions; DABT preferred; ability to travel ~20%.
2w
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ViiV Healthcare (GSK) Scientific Leader, Nonclinical Drug Discovery Modeling
Branford, Connecticut, United States
HybridFull Time
4+ YOEMS +7 years or PhD +4 years in drug discovery modeling; experience with PBPK/IVIVE/PK-PD, mechanistic modeling, reproducible coding, and cross-functional communication.
SimCYP, GastroPlus, WinNonlin, R, MATLAB, Python
2w
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ViiV Healthcare (GSK) Scientific Leader, Nonclinical Drug Discovery Modeling
Branford, Connecticut, United States
HybridFull Time
4+ YOEMS + 7 years or PhD + 4 years supporting drug discovery; experience with mechanistic/translational modeling (PBPK, IVIVE, PK/PD); familiarity with SimCYP, GastroPlus, WinNonlin and scripting in R, MATLAB, Python; strong communication.
SimCYP, GastroPlus, WinNonlin, R, MATLAB, Python
3w
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Principal Scientist, Nonclinical Drug Safety Program Discovery
Cambridge or Boston or South San Francisco or West Point or San Diego
$176k-$277k/yr HybridFull Time
8+ YOEDoctorate (PhD/DVM/MD) in relevant STEM field, 8+ years nonclinical safety experience in pharma, strong cross-functional leadership, immunology background preferred, experience with regulatory submissions.
1mo
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Pioneering Medicines: Non-Clinical Operations Specialist
Cambridge, Massachusetts, United States
$108k-$176k/yr HybridContract
3+ YOE3+ years nonclinical operations/DMPK or toxicology support; bachelor's in life sciences or project management (advanced degree preferred); GLP/regulatory familiarity; strong Excel, Word, and electronic submission tool skills; CRO coordination experience.
Microsoft Word, Microsoft Excel, electronic submission tools
1w
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Nonclinical Psychiatrist / Psychiatry Physician Author
Irving, Texas, United States
HybridPart Time
Board certified/eligible MD or DO, exceptional communication and medical knowledge, high USMLE scores, experience writing board-style questions or academic teaching preferred.
1w
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SR. RESEARCH ASSOCIATE/ASSOCIATE SCIENTIST, NONCLINICAL DEVELOPMENT
Redwood City, California, United States
$108k-$150k/yr HybridFull Time
3+ YOEBachelors+5 years or Masters+3 years in biological sciences; experience with murine in vivo models, necropsy, tissue processing, flow cytometry, qPCR/ddPCR, ELISA, IVIS imaging; strong documentation and communication skills.
IVIS, qPCR/ddPCR, ELISA, flow cytometry
2w
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Director, Study Quality and Compliance - Nonclinical Safety/Toxicology
Cambridge, Massachusetts, United States
$186k-$345k/yr HybridFull Time
10+ YOEAdvanced degree in biological sciences with 10+ years (or BS with 15+ years), GLP and toxicology experience, people leadership, SEND familiarity, and software/data management experience.
Smartsheet
1w
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Director, Toxicology
Palo Alto, California, United States
$226k-$280k/yr HybridFull Time
10+ YOEPhD/DVM-level toxicologist with ~10+ years' nonclinical safety experience, GLP knowledge, CRO management, and ability to prepare regulatory nonclinical sections.
3mo
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Scientific Writer, Integrated Research Management
Redwood City, California, United States
$143k-$178k/yr OnsiteFull Time
Advanced degree in nonclinical science; experience writing nonclinical regulatory submissions; strong pharmacology, toxicology, and DMPK expertise; ability to translate complex data into regulatory narratives.
Veeva, Regulatory information management systems, AI-enabled writing tools
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