Sr. Clinical Pharmacologist II (Associate Director), Oncology & Immuno- Oncology

Sr. Clinical Pharmacologist II (Associate Director), Oncology & Immuno- Oncology
United States - New Jersey - Morris PlainsUnited States - California - Foster City

Gilead Sciences, Inc. is a research-based bio-pharmaceutical company 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, and serious respiratory and cardiovascular conditions.

Making an impact on a global scale
Inclusion is one of the company’s five core values. That’s because we know that we are stronger and more innovative at Gilead when we are informed by a diverse set of backgrounds, experiences and points of view. Gilead Sciences is a biopharmaceutical company that discovers, develops and commercializes innovative therapeutics in areas of unmet medical need. The company's mission is to advance the care of patients suffering from life-threatening diseases worldwide.

When you join Gilead, you join our mission to change the world by enabling people to live healthier and more fulfilling lives. Come join a mission-driven bio-pharmaceutical organization that values inclusion and diversity, has a strong portfolio of products, and is constantly #CreatingPossible


Position Overview:

As a Sr. Clinical Pharmacologist II /Associate Director within the Clinical Pharmacology Group at Gilead, you will have responsibility and accountability for clinical pharmacology programs in Oncology and Immuno-Oncology. You will have unparalleled opportunity to be involved with several aspects the product development process. From first-in human through approval and post-marketing activities, you will provide input into a breadth of products within your therapeutic area. We seek to provide a rewarding career and a continuous learning experience.

Responsibilities:

• Leading complex clinical pharmacology studies
  
• Providing leadership and demonstrating accountability for the clinical pharmacology programs supporting Phase 1-4 clinical development for development compounds in your therapeutic area(s)
  
• Representing the department and providing subject matter expertise on cross-functional project teams
  
• Developing and maintaining collaborative working relationship with colleagues within and outside the department
  
• Mentoring junior level scientists, including direct reports or supporting team members
  
• Authoring/reviewing clinical protocols, analysis plans, study reports and regulatory submissions
  
• Developing high quality clinical pharmacology plans and content for global regulatory submissions, including INDs, IBs, NDAs, MAAs and pediatric plans
  
• Ensuring adherence to agreed timelines and budgets to insure prompt and accurate execution of deliverables from clinical pharmacology studies and programs
  
• Participating in and collaborating with individuals from across the business in special projects
  
• Developing and presenting training within and outside the department
  

Specific education, experience and skills required for this role:

• 7+ years' experience and a PhD, PharmD or MD degree with emphasis in clinical pharmacology, pharmacokinetics, or a related scientific discipline
  
• In-depth knowledge of pharmacokinetic and other analysis software programs (e.g. WinNonlin, GraphPad, etc.)
  
• Knowledge of current and emerging scientific standards regulatory requirements
  
• Excellent written and oral communication skills and ability to convey complex technical information clearly
  
• Ability to critically analyze problems and provide creative solutions
  
• Confidence and discipline to work autonomously
  
• Genuine curiosity and drive to ask questions - looking for the why' of every project
  
• Desire to strive for continuous improvement
  

*Preferred location: Morris Plains, NJ

For jobs in the United States:
As an equal opportunity employer, Gilead Sciences Inc. is committed to a diverse workforce. Employment decisions regarding recruitment and selection will be made without discrimination based on race, color, religion, national origin, gender, 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 careers@gilead.com for assistance.

Following extensive monitoring, research, consideration of business implications and advice from internal and external experts, Gilead has made the decision to require all U.S. employees and contractors to receive the COVID-19 vaccines as a condition of employment. “Full vaccination” is defined as two weeks after both doses of a two-dose vaccine or two weeks since a single-dose vaccine has been administered. Anyone unable to be vaccinated, either because of a sincerely held religious belief or a medical condition or disability that prevents them from being vaccinated, can request a reasonable accommodation.​

For more information about equal employment opportunity protections, please view the ‘EEO is the Law' poster.

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