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Clinical Trials Manager- Early Development Oncology

Gilead Sciences
Full-time
Remote friendly (United States)
United States
$133,195 - $172,370 USD yearly
Clinical Research and Development

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Role Summary

We are seeking a Clinical Trials Manager to support the early development oncology pipeline.

Responsibilities

  • 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 projectβ€šΓ„Γ΄s priorities within functional area.
  • Under supervision, may design scientific communications within the company.
  • Minimal travel (<10% may be required)
  • 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.

Qualifications

  • 5+ years of experience and a BS or BA in a relevant scientific discipline OR
  • 3+ years of experience and a MS in a relevant scientific discipline

Education

  • BS or BA in a relevant scientific discipline or MS in a relevant scientific discipline
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