Sr Director, Nonclinical Safety

Posted 12 Days Ago
Be an Early Applicant
Foster City, CA, USA
In-Office
261K-338K Annually
Senior level
Biotech
The Role
Leads nonclinical safety and toxicologic pathology activities supporting drug development from discovery through marketed products. Interprets and integrates anatomic and clinical pathology findings, contributes to safety strategies, regulatory interactions, submissions, mechanistic studies, and cross-functional project teams. Provides scientific leadership, mentors junior scientists, represents pathology externally, and supports diverse therapeutic areas and molecular modalities.
Summary Generated by Built In

At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across the globe. We continue to fight against the world’s biggest health challenges, and our mission requires collaboration, determination and a relentless drive to make a difference.
 

Every member of Gilead’s team plays a critical role in the discovery and development of life-changing scientific innovations. Our employees are our greatest asset as we work to achieve our bold ambitions, and we’re looking for the next wave of passionate and ambitious people ready to make a direct impact.
 

We believe every employee deserves a great leader. People Leaders are the cornerstone to the employee experience at Gilead and Kite. As a people leader now or in the future, you are the key driver in evolving our culture and creating an environment where every employee feels included, developed and empowered to fulfil their aspirations. Join Gilead and help create possible, together.
Job Description
 

The Nonclinical Sciences Department at Gilead Sciences is seeking a highly motivated veterinary anatomic pathologist to provide expert pathology and scientific support for nonclinical studies and safety strategies to support drug development from discovery through marketed products  This team-facing role involves collaboration with departmental colleagues and cross-functional teams throughout nonclinical drug development, supporting various molecular modalities, therapeutic areas, and spanning across research and regulatory pathology areas. The primary function of this role is to provide the interpretation, integration, and communication of complex anatomic and clinical pathology findings for novel therapeutics. Additional opportunities to participate in due diligence teams, serve in project team leadership roles, drive mechanistic studies, and participate in Gilead-wide working groups/cross-functional initiatives are available.

Minimum Qualifications: DVM with a PhD in a relevant biological discipline with 10+ years of relevant experience Recognized board certification in anatomic pathology. At least 8+ years of toxicologic pathology experience in a pharmaceutical R&D environment, including 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, including experience working directly on drug development project teams and Regulatory Authority interactions and submissions. Demonstrated interpersonal and communication skills.

Anatomic pathology residency training and specialty board certification 

• Previous industry experience is beneficial, though not required 

• Professional experience as a project pathologist in the biopharmaceutical industry is preferred 

• Strong decision-making, complex problem-solving, and project management skills 

• Proven strengths in critical data analysis and interpretation 

• Ability to excel in a fast-paced, dynamic, and team-oriented environment 

• Excellent verbal and written communication skills, including technical writing and presenting 

• Demonstrated scientific productivity (such as publications and conference presentations) 

• Deep experience in immunology, virology, or oncology is highly desirable 

• Experience mentoring and developing junior scientists, while fostering a culture of scientific rigor and collaboration 

• Ability to represent the nonclinical pathology function in external scientific forums/consortia, cross-functional strategic discussions, and regulatory interactions 

• Working knowledge of digital pathology, image analysis, and AI is desirable 


 

The salary range for this position is: $261,375.00 - $338,250.00. Gilead considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.


For jobs in the United States:

Gilead Sciences Inc. is committed to providing equal employment opportunities to all employees and applicants for employment, and is dedicated to fostering an inclusive work environment comprised of diverse perspectives, backgrounds, and experiences. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, sex, age, sexual orientation, physical or mental disability, genetic information or characteristic, gender identity and expression, veteran status, or other non-job related characteristics or other prohibited grounds specified in applicable federal, state and local laws. In order to ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Era Veterans' Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact [email protected] for assistance.

For more information about equal employment opportunity protections, please view the 'Know Your Rights' poster.

NOTICE: EMPLOYEE POLYGRAPH PROTECTION ACT
YOUR RIGHTS UNDER THE FAMILY AND MEDICAL LEAVE ACT

Gilead Sciences will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, (c) consistent with the  legal duty to furnish information; or (d) otherwise protected by law.
 

Our environment respects individual differences and recognizes each employee as an integral member of our company. Our workforce reflects these values and celebrates the individuals who make up our growing team.

Gilead provides a work environment free of harassment and prohibited conduct. We promote and support individual differences and diversity of thoughts and opinion.


For Current Gilead Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

Skills Required

  • DVM with a PhD in a relevant biological discipline
  • 10+ years of relevant professional experience
  • Recognized board certification in anatomic pathology
  • Anatomic pathology residency training
  • At least 8 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
  • Understanding of drug discovery, development, and regulatory processes
  • Experience working on drug development project teams and with Regulatory Authority interactions and submissions
  • Issue-resolution, decision-making, complex problem-solving, project management, and critical data analysis skills
  • Excellent verbal and written communication, technical writing, and presentation skills
  • Scientific productivity through publications or conference presentations
  • Ability to mentor and develop junior scientists
  • Previous industry experience
  • Professional experience as a project pathologist in the biopharmaceutical industry
  • Deep experience in immunology, virology, or oncology
  • Working knowledge of digital pathology, image analysis, and AI

Gilead Sciences Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Gilead Sciences and has not been reviewed or approved by Gilead Sciences.

  • Fair & Transparent Compensation Pay is considered competitive and fair relative to roles, frequently cited as a standout strength. Feedback suggests compensation compares well within biotech and is a notable reason employees feel valued.
  • Equity Value & Accessibility Stock awards and an employee stock purchase program are consistently described as meaningful parts of total compensation. Equity components are seen as accessible and enhance long‑term wealth building.
  • Retirement Support A strong company 401(k) match with immediate vesting is often singled out as a differentiator. This support is perceived to significantly boost long‑term financial security.

Gilead Sciences Insights

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The Company
HQ: Foster City, CA
14,337 Employees
Year Founded: 1987

What We Do

The way we see it, the impossible is not impossible. It’s simply what hasn’t been achieved yet. For more than 30 years, we’ve pursued it, chased it down, tackled it for answers and surrounded it for a way in. We have worked tirelessly to bring forward medicines for life-threatening diseases. Creating Possible drives everything we do. It’s evident in our mission and core values. This is how we built a culture of excellence that is fueled by a passion for improving lives of people around the world. For us, nothing is impossible – because of the people we work with, the communities we stand with and the partners we push forward with. Our ~12,000 employees band together through science, grit, compassion and courage to prove the impossible wrong. At Gilead, the tangible results of your contributions are evident. Where every individual matters. Where all employees can enhance their skills through ongoing development. And where we start every day with one question: “What’s next?” Social Media Guidelines: https://gilead.inc/3t1m7d5

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