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Gilead Sciences
Gilead Sciences
H1B Visa SponsorBiotechnologyConsultingHealthcare
Gilead Sciences is a biopharmaceutical company developing and delivering medicines for life-threatening diseases. Its work has a strong focus on virology, including HIV and hepatitis, alongside growing research in oncology and inflammation. The company supports a global portfolio of more than 25 products and 50 clinical programs, while also investing in HIV research and health-equity initiatives. For job seekers, Gilead Sciences offers opportunities to contribute to research, development, and healthcare programs aimed at improving patient outcomes worldwide.
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Senior Director of Nonclinical Safety

Lead nonclinical safety and toxicologic pathology at Gilead Sciences, supporting biopharmaceutical research and development. Guide regulatory work, pathology programs, and drug development teams.

USUnited States
$237,575 – $307,450 / year
RemoteFull-timeSeniorEnglish RequiredDirector

Description

  • Provide nonclinical safety and toxicologic pathology expertise across pharmaceutical research and development.
  • Support screening, IND-enabling, and development studies involving rodent and non-rodent species.
  • Collaborate directly with drug development project teams.
  • Contribute to interactions with regulatory authorities and regulatory submissions.
  • Bring innovative, adaptable, and critical thinking to research and development pathobiology.
  • Apply modern pathology laboratory technologies, including assay development, implementation, and interpretation.
  • Mentor and encourage colleagues in matrix and line organizations.
  • Lead teams and delegate responsibilities effectively across the organization.

Requirements

  • DVM or MD, a PhD in a relevant biological discipline, and at least 8 years of relevant experience.
  • Board certification in anatomic pathology.
  • At least 5 years of toxicologic pathology experience in pharmaceutical research and development.
  • Experience with screening, IND-enabling, and development studies in rodent and non-rodent species.
  • Demonstrated ability to resolve issues.
  • Strong understanding of drug discovery, development, and regulatory processes.
  • Experience working directly with drug development project teams and participating in regulatory authority interactions and submissions.
  • Evidence of innovative, adaptable, and critical thinking applied to research and development pathobiology.
  • Demonstrated interpersonal and communication skills.
  • Ability to present opinions and expertise with confidence, authority, respect, and diplomacy to Gilead colleagues at all levels and to external partners.
  • Strong leadership and delegation skills, including success mentoring and motivating people in matrix or line organizations.
  • Working knowledge of modern pathology laboratory technologies, including assay development, implementation, and interpretation.
  • Preferred: Experience with translational or clinical biomarkers and/or research pathology in pharmaceutical research and development.
  • Preferred: Experience developing molecular pathology assays (IHC, ISH, RNASeq, qPCR, or LCM), integrating and analyzing data, and interpreting image analysis.

Benefits

  • Discretionary annual bonus.
  • Discretionary long-term stock-based incentives.
  • Paid time off.
  • Company-sponsored medical insurance.
  • Company-sponsored dental insurance.
  • Company-sponsored vision insurance.
  • Company-sponsored life insurance.
  • Benefits package.

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