Scientist, Nonclinical Safety
Gilead SciencesAbout the role
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
Gilead Sciences, Inc. is a research-based biopharmaceutical company headquartered in Foster City, California that discovers, develops and commercializes innovative medicines in areas of unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of patients living with life-threatening diseases around the world. Gilead’s therapeutic areas of focus include HIV/AIDS, liver diseases, cancer and inflammation.
Gilead’s core values of integrity, inclusion, teamwork, excellence, and accountability shape our culture and are the foundation of our future success. Challenge yourself and make a difference in the world – Being Here Matters.
Job Description
We are seeking a bright and enthusiastic Research Scientist to complement our Nonclinical Safety and Pathobiology group. Gilead is a fast-paced, data-driven, scientifically rigorous organization, and the role will suit a scientist who is able to thrive in this type of environment. The primary responsibility is to serve as the toxicology representative on multifunctional project teams, including ownership of the nonclinical safety program and contributing to regulatory documents to support drug development candidates across a variety of platforms from early research through registration/post approval.
Key Aspects:
- Manage multiple projects simultaneously with minimal supervision.
- Provide critical review and interpretation of protocols, data and study reports
- Actively support the integration of early nonclinical safety strategies throughout Research.
- Solve moderately complex problems requiring thorough scientific assessment.
- Effectively communicate project development plans and study results to project teams and Senior level management
- Team player who thrives in a high-speed environment where autonomy, accountability and innovation are critical for success.
- Excellent self-management and organizational skills, and ability to manage high volume workload
- Clear and concise, oral and written communication skills
- Strong motivation, independence, and the ability to work in a multidisciplinary, matrix environment with minimal supervision.
Knowledge:
- Good scientific expertise in subject area/discipline; familiar with other disciplines inside and/or outside of department (e.g., pathology, pharmacology, drug metabolism).
- Familiarity with ICH and GLP
Education and Experience:
- PhD in toxicology, pharmacology, or related scientific discipline
- 2+ years experience in small molecule and/or biopharmaceutical drug development desirable
or
- BS or MS, and extensive industry experience in nonclinical safety assessment
- Board certification or eligibility is desirable.
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