Senior Director, Nonclinical Safety

🔥 0 minutes ago

🇺🇸 United States – Remote

💵 $237.6k - $307.4k / year

⏰ Full Time

🟠 Senior

👔 Director

🦅 H1B Visa Sponsor

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Gilead Sciences

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1987

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

Healthcare • Consulting • Biotechnology

Gilead Sciences is a leading biopharmaceutical company that focuses on discovering, developing, and delivering innovative therapeutics for patients with life-threatening diseases. The company is highly recognized for its contributions in virology, particularly HIV and hepatitis, and is actively expanding its therapeutic reach into fields like oncology and inflammation. Gilead has a strong pipeline of medicines, with over 25 products available globally and 50 clinical programs. Known for its commitment to health equity, the company also actively funds HIV research and causes. Gilead's dedication to scientific innovation and health equity aims to tackle the world's most pressing health challenges, improving patient lives globally.

📋 Description

• Provide nonclinical safety and toxicologic pathology expertise in pharmaceutical R&D • Support screening, IND-enabling and development studies in rodent and non-rodent species • Work directly on drug development project teams • Participate in Regulatory Authority interactions and submissions • Apply innovative, flexible and critical thinking to R&D pathobiology • Use modern pathology laboratory technologies, including assay development, application and interpretation • Mentor and motivate people in matrix and/or line organizations • Lead and delegate effectively across the organization

🎯 Requirements

• DVM or MD, with a PhD in a relevant biological discipline and 8+ years of relevant experience • Recognized board certification in anatomic pathology • At least 5+ years of toxicologic pathology experience in a pharmaceutical R&D environment • Experience with screening, IND-enabling and development studies in rodent and non-rodent species • Demonstrated issue-resolution experience • High level of understanding of the drug discovery, development and regulatory process • Experience working directly on drug development project teams and Regulatory Authority interactions and submissions • Demonstrated innovative, flexible and critical thinking applied to R&D pathobiology • Demonstrated interpersonal and communication skills • Ability to project opinions and knowledge with confidence, authority, respect and diplomacy when interacting with all levels of Gilead colleagues and external partners • Excellent leadership and delegation skills demonstrated by successfully mentoring and motivating people in a matrix and/or line organization • Working knowledge of modern pathology laboratory technologies, including assay development, application and interpretation • Preferred: Experience of translational/clinical biomarker and/or research pathology in a pharmaceutical R&D environment • Preferred: Experience of molecular pathology assay development (IHC, ISH, RNASeq, qPCR, LCM), data integration and analysis, image analysis and interpretation

🏖️ Benefits

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