Gilead Sciences Inc

Clinical Trials Manager

Gilead Sciences Inc$133K — $172K *
Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • BS or BA in a relevant scientific discipline or RN license with 6+ years of relevant experience.
  • Thorough understanding of FDA/EMEA Regulations, ICH Guidelines, and GCPs.
  • Expertise in clinical trials management and organizational perspectives.
  • Proven ability to manage multiple tasks and participate in strategic initiatives.
  • Experience in Hematology, Oncology, Rheumatology, or Autoimmune disorders is a plus.

Responsibilities

  • Coordinate and supervise all aspects of clinical studies.
  • Assist Clinical Program Manager with overall study management.
  • Draft and coordinate review of study-related documents.
  • Maintain study timelines and contribute to budget development.
  • Manage CROs and vendors, ensuring efficient collaboration.
  • Review data listings and assist in preparing clinical study reports.
  • Train CROs, vendors, and site staff on study requirements.

Benefits

  • Company-sponsored medical, dental, vision, and life insurance plans.
  • Eligible for discretionary annual bonus and stock-based long-term incentives.
  • Paid time off and a comprehensive benefits package.
  • Opportunities for professional development and career growth.
Full Job Description

Job Description

As a Clinical Trials Manager at Gilead/Kite, you will be responsible for:

  • Coordinating and supervising all aspects of a clinical study. Monitors clinical trial sites.

  • Assists Clinical Program Manager in overall study management.

  • Drafts and coordinates review of relevant documents including protocols, informed consents, case report forms, monitoring plans, investigator brochures, and clinical study reports.

  • Maintains study timelines.

  • Contributes to development of study budget.

  • Contributes to development of RFPs and participate in selection of CROs/vendors.

  • Manage CROs/vendors.

  • Coordinates review of data listings and preparation of interim/final clinical study reports.

  • May contribute to development of abstracts, presentations, and manuscripts,
    Ensures effectiveness of site budget/contract process.

  • May be asked to train CROs, vendors, investigators, and study coordinators on study requirements.

  • Assists in determining the activities to support a project’s priorities within functional area.

  • Under supervision, may design scientific communications within the company.

  • Excellent teamwork, communication, decision-making and organizational skills are required.

  • Thorough knowledge and understanding of FDA and/or EMEA Regulations, ICH Guidelines, and GCPs governing the conduct of clinical trials is desirable.

  • Must be able to generally understand, interpret, and explain protocol requirements to others.

  • Must be able to prioritize multiple tasks.
    May serve as a resource for others within the company for clinical trials management expertise.

  • Under general supervision, is able to examine functional issues from an organizational perspective.

  • Must be able to participate in multiple departmental or interdepartmental strategic initiatives under limited supervision.

  • Must have a general, functional expertise to support SOP development and implementation.

  • Travel is required.

Basic Qualifications:

BS or BA in a relevant scientific discipline and 6 + years of relevant experience OR
RN license (2 or 3 year certificate) and 6 + years of relevant experience.

Preferred Qualifications:

Experience in the following therapy areas is helpful: Hematology, Oncology, Rheumatology, Autoimmune disorders,

Familiarity and experience with In-Vivo studies.

People Leader Accountabilities:

•Create Inclusion - knowing the business value of diverse teams, modeling 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, and organizational objectives, and holding them to account. They provide the support needed to remove barriers and connect their team to the broader ecosystem.


The salary range for this position is:

Bay Area: $146,540.00 - $189,640.00.Other US Locations: $133,195.00 - $172,370.00.


Kite considers a variety of factors when determining base compensation, including experience, qualifications, and geographic location. These considerations mean actual compensation will vary. This position may also be eligible for a discretionary annual bonus, discretionary stock-based long-term incentives (eligibility may vary based on role), paid time off, and a benefits package. Benefits include company-sponsored medical, dental, vision, and life insurance plans*.
 

For additional benefits information, visit:

https://www.gilead.com/careers/compensation-benefits-and-wellbeing

* Eligible employees may participate in benefit plans, subject to the terms and conditions of the applicable plans.


Kite is a biopharmaceutical company engaged in the development of innovative cancer immunotherapies with a goal of providing rapid, long-term durable response and eliminating the burden of chronic care. The company is focused on chimeric antigen receptor (CAR) and T cell receptor (TCR) engineered cell therapies designed to empower the immune system's ability to recognize and kill tumors. Kite is based in Santa Monica, CA. For more information on Kite, please visit www.kitepharma.com. Sign up to follow @KitePharma on Twitter at www.twitter.com/kitepharma.
 

For Current Kite Pharma Employees and Contractors:

Please apply via the Internal Career Opportunities portal in Workday.

About Gilead Sciences Inc

Gilead Sciences is a research-based biopharmaceutical company that discovers, develops, and commercializes innovative medicines in areas of unmet need. With each new discovery and experimental drug candidate, they seek to improve the care of patients suffering from life-threatening diseases. Gilead's primary areas of focus include HIV/AIDS, liver disease, and serious cardiovascular and respiratory conditions.

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Learn more about Gilead Sciences Inc
Size
14,400 employees
Market Cap
$107.2 billion
Industry
Net Income
$123 million
Founded
1987
5 Year Trend
-2.1%
Revenue
$24.6 billion
NASDAQ

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