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Clinical Program Manager - Oncology

Gilead Sciences, Inc.
Foster City
See job description.
Closing date
Oct 7, 2021

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Health Sciences, Clinical Research
Position Type
Full Time
Job Type
Lab Manager
Organization Type
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Clinical Program Manager - Oncology
United States - California - Foster CityUnited States - New Jersey - Morris PlainsUnited States - Washington - Seattle

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. Gileads 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 companys five core values. Thats 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

Clinical Program Manager, Clinical Operations- Oncology

**Location: This position can be located in either Foster City, CA, Morris Plains, NJ or Seattle, WA**

We are seeking a talented, experienced, and highly motivated candidate to join the Oncology Clinical Operations team. The candidate must have the ability to work independently, be an effective leader, and an engaged team member in a dynamic, fast-paced environment.

Specific Responsibilities and Skills for Position:

- Must meet all requirements for Sr. Clinical Trials Manager (Sr. CTM), Clinical Operations position and have demonstrated proficiency in all relevant areas

- Oversees successful implementation of Gilead (GS), Collaborative (CO), Investigator Sponsored Research (ISR) program, expanded access programs, and compassionate use programs

- For GS studies, ability to write study protocols, study reports, and regulatory documents (e.g. IND, NDA, PRAC etc.) with little supervision

- Contributes to development of abstracts, presentations, and manuscripts

- For GS, CO, and ISR studies, must have a demonstrated ability to successfully develop, implement, manage and complete clinical trials

- Provides guidance and oversight for the successful management of all aspects of international clinical trials within designated program budgets and timelines

- Experience in managing staff as well as mentoring and developing junior staff is required

-Partners with cross functional teams to manage, adjust, and revise project timelines/budgets as necessary

- Communicates project status and issues and ensure project team goals are met

- May represent the company at professional events

- May represent the department at cross-departmental events

- Experience in developing RFPs and selection and management of CROs/vendors

- Functional expertise to initiate, author, or contribute to SOP development, implementation and training

- Recruits, hires, mentors and manages CPA/CTMA/Sr. CTMA/CTM/Sr. CTM direct reports and supports their professional development

- Anticipates moderately complex obstacles and client difficulties and implements solutions to achieve project goals

- Must be able to resolve problems using national and international regulations, guidelines and investigator interaction

- Collaborates with local medical affairs colleagues on country specific studies and initiatives

- Provides knowledge and expertise on country specific regulations, site experience, and suitability for development studies

- Independently manages all components of complex studies, compassionate use programs and non-interventional studies


- Excellent interpersonal skills and demonstrated ability to lead is required

- May design and use all available vehicles for scientific communication within company. With limited supervision may participate in or lead departmental strategic initiatives

- Ability to participate in and/or lead departmental or interdepartmental strategic initiatives under limited supervision

- Ability to examine functional issues from a broader organizational perspective

- Strong communication and influence skills and ability to create a clear sense of direction is necessary

- Thorough knowledge and understanding of FDA and/or EMA Regulations (or relevant local regulations), ICH Guidelines, and GCPs governing the conduct of clinical trials and non-interventional studies

Experience and Skills:

- At least 8+ years of experience and a BS or BA in a relevant scientific discipline

- At least 8+ years of experience and an RN (2 or 3 year certificate)

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 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.\u200b

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



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:

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