Getting Hired
About Gilead
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. Role Overview
Director, Pharmacometrics – lead quantitative analyses across Oncology, Inflammation, and Virology therapeutic areas from first-in human through Phase IV clinical trials. Champion model-informed drug development (MIDD) and serve as subject matter expert for modeling and simulation across cross‑functional partners. Responsibilities
Lead quantitative and innovative strategies within clinical pharmacology to impact MIDD during the life cycle of the program. Evaluate and apply state‑of‑the‑art quantitative pharmacology approaches for clinical decision‑making and global regulatory submissions (INDs, IBs, NDAs, BLAs, MAAs, pediatric plans). Guide dose regimen/optimization strategies in partnership with therapeutic area leads and clinical pharmacology leads to enable data‑driven decisions. Develop, author, review, approve modeling and simulation strategy, analysis plans, outputs, and key findings for regulators and stakeholders. Ensure adherence to agreed timelines and budgets to ensure prompt and accurate execution of deliverables from clinical pharmacology studies and programs. Develop and present training within and outside the department as needed. Basic Qualifications
PhD or equivalent degree in engineering, pharmaceutical sciences, pharmacology, or related discipline with 0+ years of relevant pharmacometrics research or development experience OR Masters or equivalent degree in engineering, pharmaceutical sciences, pharmacology, or related discipline with 6+ years of relevant pharmacometrics research or development experience OR Bachelors or equivalent degree in engineering, pharmaceutical sciences, pharmacology, or related discipline with 8+ years of relevant pharmacometrics research or development experience. Preferred Qualifications
Significant experience working on, with, and leading cross‑functional project/program teams in life sciences. Extensive experience in pharmacometrics leading and authoring modeling and simulation plans and having responsibility for the scientific execution of related analyses across Phase I – IV studies. Demonstrated excellence in effectively managing multiple pharmacometrics analyses deliverables and priorities through matrix management and leadership. Relevant experience in the Oncology, Virology, and/or Inflammation Therapeutic Areas. Proficiency in mathematics, strong communication and organizational skills, and demonstrated ability to be a fast learner, flexible and adaptable to change. Compensation & Benefits
Base salary range: $146,540.00 – $189,640.00.
Eligible for discretionary annual bonus, discretionary stock‑based long‑term incentives, paid time off, and a benefits package that includes company‑sponsored medical, dental, vision, and life insurance plans.
For additional benefits information, visit compensation‑benefits‑and‑wellbeing page. Equal Employment Opportunity
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. Employment decisions 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. For more information about equal employment opportunity protections, please view the Know Your Rights poster.
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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. Role Overview
Director, Pharmacometrics – lead quantitative analyses across Oncology, Inflammation, and Virology therapeutic areas from first-in human through Phase IV clinical trials. Champion model-informed drug development (MIDD) and serve as subject matter expert for modeling and simulation across cross‑functional partners. Responsibilities
Lead quantitative and innovative strategies within clinical pharmacology to impact MIDD during the life cycle of the program. Evaluate and apply state‑of‑the‑art quantitative pharmacology approaches for clinical decision‑making and global regulatory submissions (INDs, IBs, NDAs, BLAs, MAAs, pediatric plans). Guide dose regimen/optimization strategies in partnership with therapeutic area leads and clinical pharmacology leads to enable data‑driven decisions. Develop, author, review, approve modeling and simulation strategy, analysis plans, outputs, and key findings for regulators and stakeholders. Ensure adherence to agreed timelines and budgets to ensure prompt and accurate execution of deliverables from clinical pharmacology studies and programs. Develop and present training within and outside the department as needed. Basic Qualifications
PhD or equivalent degree in engineering, pharmaceutical sciences, pharmacology, or related discipline with 0+ years of relevant pharmacometrics research or development experience OR Masters or equivalent degree in engineering, pharmaceutical sciences, pharmacology, or related discipline with 6+ years of relevant pharmacometrics research or development experience OR Bachelors or equivalent degree in engineering, pharmaceutical sciences, pharmacology, or related discipline with 8+ years of relevant pharmacometrics research or development experience. Preferred Qualifications
Significant experience working on, with, and leading cross‑functional project/program teams in life sciences. Extensive experience in pharmacometrics leading and authoring modeling and simulation plans and having responsibility for the scientific execution of related analyses across Phase I – IV studies. Demonstrated excellence in effectively managing multiple pharmacometrics analyses deliverables and priorities through matrix management and leadership. Relevant experience in the Oncology, Virology, and/or Inflammation Therapeutic Areas. Proficiency in mathematics, strong communication and organizational skills, and demonstrated ability to be a fast learner, flexible and adaptable to change. Compensation & Benefits
Base salary range: $146,540.00 – $189,640.00.
Eligible for discretionary annual bonus, discretionary stock‑based long‑term incentives, paid time off, and a benefits package that includes company‑sponsored medical, dental, vision, and life insurance plans.
For additional benefits information, visit compensation‑benefits‑and‑wellbeing page. Equal Employment Opportunity
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. Employment decisions 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. For more information about equal employment opportunity protections, please view the Know Your Rights poster.
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