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Clinical Trial Manager - Oncology

Gilead Sciences, Inc.

Foster City (CA)

On-site

USD 146,000 - 190,000

Full time

6 days ago
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Job summary

A leading biopharmaceutical company is seeking a Clinical Trial Manager for their Oncology team. The role involves managing clinical trials, ensuring compliance with regulations, and collaborating with various departments. Ideal candidates will have significant experience in oncology trials and strong organizational skills. This position is based in either Foster City, CA or Parsippany, NJ, and is not remote.

Benefits

Bonuses
Stock incentives
Benefits

Qualifications

  • Minimum 5+ years of experience required.
  • Experience with oncology clinical trials preferred.

Responsibilities

  • Draft and review documents such as protocols and study reports.
  • Maintain study timelines and coordinate data reviews.
  • Train CROs, vendors, and investigators on study requirements.

Skills

Teamwork
Communication
Decision-Making
Organizational Skills

Education

BS/BA in a relevant discipline
Master’s degree or higher

Tools

Word
PowerPoint
Excel

Job description

Clinical Trial Manager - Oncology page is loaded

Clinical Trial Manager - Oncology
Apply locations United States - California - Foster City United States - New Jersey - Parsippany time type Full time posted on Posted 11 Days Ago job requisition id R0045224

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

CLINICAL OPERATIONS: Clinical Operations is responsible for executing all Phase 1-4 clinical trials globally. Collaborating with Clinical Research, Medical Affairs, and Development, ensures all activities comply with SOPs, policies, and regulations to deliver high-quality data supporting product registration and commercialization.

Led by experienced professionals, careers in Clinical Operations offer rapid knowledge growth in a supportive environment. The Clinical Trials Manager, Oncology (CTM) role involves joining the Oncology Clinical Operations team.

This position can be located in Foster City, CA or Parsippany, NJ. This is NOT a remote position.

RESPONSIBILITIES:

  • Draft and review documents such as protocols, informed consents, case report forms, monitoring plans, investigator brochures, and study reports.
  • Understand, interpret, and explain protocol requirements.
  • Maintain study timelines.
  • Coordinate review of data listings and prepare interim/final reports.
  • Support project activities within the functional area.
  • Contribute to RFP development and vendor selection.
  • Train CROs, vendors, investigators, and coordinators on study requirements as needed.
  • Assist in developing study budgets.
  • Serve as a resource for clinical trials management expertise.
  • Address organizational issues from a functional perspective.
  • Participate in recruiting and hiring processes, supporting professional development.
  • Contribute to scientific communications, including abstracts, presentations, and manuscripts.
  • Design scientific communications under supervision.
  • Participate in departmental initiatives with limited supervision.
  • Support SOP development and implementation.
  • Travel may be required.

KNOWLEDGE:

  • Strong teamwork, communication, decision-making, and organizational skills.
  • Thorough knowledge of FDA/EMA regulations, ICH Guidelines, and GCP.
  • Proficiency with Word, PowerPoint, and Excel.

SKILLS:

  • Minimum 5+ years of experience and BS/BA in a relevant discipline, OR
  • Minimum 3+ years of experience with a Master’s degree or higher; scientific discipline preferred.
  • Experience with oncology clinical trials.
The salary range is $146,540.00 - $189,640.00, with potential bonuses, stock incentives, benefits, and other perks. For more info, visit: https://www.gilead.com/careers/compensation-benefits-and-wellbeing

Gilead is committed to equal employment opportunities and fostering an inclusive environment. Applicants requiring accommodations can contact ApplicantAccommodations@gilead.com.

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