Gilead Sciences, Inc. Posted August 3, 2026

VP, NonClinical Safety and Pathobiology

Foster City, United States Full time
Drug Discovery & Preclinical Research Executive/VP

Gilead Sciences, Inc. is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

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

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.

Key Responsibilities:

Nonclinical Safety and Pathobiology (NSP) group is responsible for design, implementation, oversight and analysis of nonclinical programs to support drug development candidates from research to registration.

NSP group is comprised of Toxicology, Pathology, and Environmental / Occupational Toxicology.

NSP is responsible for ensuring patient safety of Gilead drug candidates through exhaustive non-clinical evaluations.

NSP is responsible for ensuring global compliance with worldwide regulations governing the conduct  of Gilead’s nonclinical studies in support of global clinical trials, registration, and new drug approvals.

NSP is responsible for Pathobiology characterization of animal models and clinical specimens as needed to advance translational understanding of new targets and new therapeutics.

Manages and mentors a group of Ph.D. level toxicologists and pathologists to ensure NSP continues to develop and implement cutting edge scientific technologies and drug development strategies.

Prepares and reviews regulatory documents including INDs/IMPDs, Investigator Brochures and NDAs/MAAs.

Communicates successfully cross-functionally to accomplish Company goals.

Solves highly complex problems requiring evaluation of business intangibles in addition to thorough scientific assessment.

Knowledge:

Experience in successful conduct of nonclinical programs as well as preparation, submission and approval of nonclinical sections of regulatory filings covering all stages of development.

Has an in-depth knowledge of nonclinical drug discovery and development and regulatory environments in the US, EU and AsiaPac.

Individual is recognized as an expert in the field both inside and outside of the company.

Possesses strong leadership/management abilities and is highly effective on teams.

Possesses strong organizational skills, technical excellence, scientific creativity and critical thinking ability.

Maintains broad knowledge of scientific discipline. Expected to provide oversight of the following areas:

Discovery support screening studies for candidate selection

Development support GLP toxicity studies (to enable IND/IMPD and NDA/MAA submissions)

Preparation of nonclinical regulatory documentation

Issue resolution

Qualification of impurities

Environmental assessments

Specific Education and Experience Requirements

Requires a Ph.D in pharmacology/toxicology/pathology or related scientific discipline, together with a significant amount of experience that has led to a reputation as a leader in the field.

DABT and/or DACVP and/or ERT preferred.

Knowledge of global regulatory guidelines associated with quality and compliance in the conduct of nonclinical safety studies is required.

Should have at least 20 years of experience in research or development in a pharmaceutical company or contract research organization.

Ability to collaborate across a global network of stakeholders to ensure delivery of drug candidates.

People Leader Accountabilities

Create Inclusion - knowing the business value of diverse teams, modelling inclusion and embedding the value of diversity in the way they manage their teams.

Develop Talent - understand the skills, experience, aspirations and potential of their employees and coach them on current performance and future potential. They ensure employees are receiving the feedback and insight needed to grow, develop and realize their purpose.

Empower Teams - connect the team to the organization by aligning goals, purpose, organizational objectives and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.

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 ApplicantAccommodations@gilead.com  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.

Job details

Seniority
Executive/VP
Function
Drug Discovery & Preclinical Research
Therapeutic area
Not listed
Location
Foster City, United States
Employment type
Full time

How this role compares

Computed from every other active Drug Discovery & Preclinical Research role in our database, not just this employer's listings.

We currently track 19 comparable Executive/VP Drug Discovery & Preclinical Research roles across 7 biopharma companies.

19Comparable roles tracked
18Currently active
7Companies hiring similar roles
2Countries represented

Salary context

12 of 19 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Peer group range $202,950 – $322,650 (median $260,300)

Where these roles are based

Top locations among the 19 comparable roles

United States18
India1

Seniority mix

19 of 19 peers have a known seniority level

Senior Director12
Executive/VP7

Therapeutic area mix

3 of 19 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology3

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Lilly San Francisco, California, United States of America Executive/VP
Same function Same seniority Same country
60%similar
Lilly Indianapolis, Indiana, United States of America Executive/VP
Same function Same seniority Same country
60%similar
Lilly San Francisco, California, United States of America Executive/VP
Same function Same seniority Same country
60%similar
Amgen Inc. South San Francisco, United States Executive/VP
Same function Same seniority Same country
60%similar
Amgen Inc. South San Francisco, United States Executive/VP
Same function Same seniority Same country
60%similar
AstraZeneca Boston, Massachusetts, United States of America Executive/VP
Same function Same seniority Same country

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Director/Sr. Director/Exec. Director, Molecular Pharmacology (AMD)
Lilly · San Francisco, California, United States of America · Executive/VP
Function Therapeutic area Seniority Country
60%
Executive Director, Research – Technology & Innovation for Inflammation Discovery
Amgen Inc. · South San Francisco, United States · Executive/VP
Function Therapeutic area Seniority Country
50%
Director/Senior Director, ADMET & PK/PD Modeling
Lilly · Indianapolis, Indiana, United States of America · Senior Director
Function Therapeutic area Adjacent seniority Country
50%
Senior Director , Quantitative Pharmacology
Regeneron Pharmaceuticals, Inc (USA) · Tarrytown, United States · Senior Director
Function Therapeutic area Adjacent seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.