Non-Clinical Toxicology Manager

AstraZeneca
Barcelona
Workplace: HybridFull timeFunction: Research & Scientific (R&D)Experience: 3-5 yearsEducation: mastersSkills: ["Critical thinking","Interpersonal skills","Communication","Organizational skills","Project management"]

Lead preclinical toxicology programs for rare disease drug development, partnering with global project teams, regulatory affairs, and clinical stakeholders. Oversee CROs in the design, execution, reporting, and quality of studies covering pharmacokinetics, toxicology, reproduction toxicology, genotoxicity, carcinogenicity, and safety pharmacology. Manage study issues, ensure GLP and regulatory compliance, interpret data, and communicate results to teams and management.

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AstraZeneca
AstraZeneca
1 day ago

Non-Clinical Toxicology Manager

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Job Summary

Lead preclinical toxicology programs for rare disease drug development, partnering with global project teams, regulatory affairs, and clinical stakeholders. Oversee CROs in the design, execution, reporting, and quality of studies covering pharmacokinetics, toxicology, reproduction toxicology, genotoxicity, carcinogenicity, and safety pharmacology. Manage study issues, ensure GLP and regulatory compliance, interpret data, and communicate results to teams and management.
Location: Barcelona
Workplace: Hybrid
Employment Type: Full time
Job Function: Research & Scientific (R&D)

Key Responsibilities

  • •Support preclinical development programs by bringing scientific and technical expertise to early-stage drug development teams.
  • •Oversee CROs on study design, implementation, management, and reporting for pharmacokinetics and toxicology-related studies.
  • •Serve as primary contact with CROs for contracts, invoices, study setup, monitoring, onsite visits, and reporting.
  • •Identify and resolve scientific, technical, logistical, and quality issues to keep studies compliant and on track.
  • •Review, analyze, and interpret data; coordinate review and finalization of reports and communicate results to project teams and management.

Key Requirements

  • •PharmD, VetD, or a master’s degree in biology, animal sciences, toxicology, or a related field.
  • •3-5 years of experience as a toxicology study director/monitor in pharma, biotech, or a CRO setting.
  • •Demonstrated expertise managing nonclinical studies, including Good Laboratory Practices (GLP) fundamentals and data interpretation.
  • •Experience ensuring successful study execution within allocated budgets and timelines.
  • •Strong communication, organizational, planning, and project management skills; fluent English written and spoken.
Experience:3-5 yearsPharmaBiotechCRO
Education:Master's in biology, animal sciences, toxicology or related fields
Skills:Critical thinkingInterpersonal skillsCommunicationOrganizational skillsProject management
Languages:English
Tech Stack:GLPPharmacokinetics

Company Brief

AstraZeneca
Global biopharmaceutical company discovering, developing and commercializing prescription medicines across oncology, cardiovascular, renal & metabolism, respiratory, and immunology, focused on innovative therapies and vaccines to improve patient outcomes worldwide.
Industry: Pharmaceuticals
Company Size: Enterprise (1,001+ employees)
Revenue: USD 1B+
Growth: Public Company
Valuation: Public Company (Market Cap in USD)
Funding: IPO / Publicly Listed
Headquarters: Cambridge, United Kingdom
Founded: 1999
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