Global Clinical Trial Leader

San Francisco, CA, US • Posted 7 hours ago • Updated 7 hours ago
Contract Corp To Corp
Contract W2
12 Months
On-site
Depends on Experience
Fitment

Dice Job Match Score™

👾 Reticulating splines...

Job Details

Skills

  • Global Clinical Trial Leader

Summary

We are looking for Global Clinical Trial Leader for our client in San Francisco, CA

Job Title: Global Clinical Trial Leader

Job Location: San Francisco, CA

Job Type: Contract

Job Overview:

Pay Range: $87.18/hr - $92.18/hr

Requirement/Must Have:

  • Bachelor s degree or equivalent required (scientific or healthcare discipline preferred).
  • 8+ years of clinical study management experience desired.
  • Working knowledge of Google Cloud Platform/ICH requirements, international regulatory guidelines, and the end to end drug development process.
  • Some travel may be required.

Responsibilities:

  • Provide operational guidance to one or more global cross-functional Protocol Execution Teams (PETs) across all study stages (start-up, conduct, and close-out).
  • Foster a positive work environment built on mutual respect, innovation, and accountability at both local and global project levels.
  • Drive and finalize cross-functional activities ensuring the quality delivery of vendor specifications, drug supply forecasting, monitoring/communication plans, Trial Master Files (TMF), and CTMS data.
  • Collaborate with cross-functional members on study plans and coordinate effective investigator meetings.
  • Participate in vendor selection alongside the PETL; oversee outsourced activities to ensure CROs and vendors deliver strictly against contracted scopes of work.
  • Provide strategic input into the overall study budget and directly manage assigned vendor budgets.
  • Contribute to country and site selection, assist in developing clinical trial protocols/informed consents, and provide operational input on protocol feasibility.
  • Apply critical thinking to manage timelines, identify bottlenecks, and propose actionable resolutions.
  • Maintain a patient and site-centric mindset across all trial activities and interactions.
  • Partner with gRED and pan-Roche colleagues to establish operational best practices and enhance clinical trial execution across the organization.
  • Serve as a Subject Matter Expert (SME) or gRED single point of contact for targeted functional initiatives.
  • Coach, mentor, and share expertise to support the development of junior staff and peers.

Skills:

  • Excellent communication skills with the ability to independently deliver key messages to stakeholders, influence teams, and negotiate to achieve shared goals.
  • Creative problem solver who welcomes diversity of thought to navigate through ambiguity and resolve issues.
  • Highly flexible, solution-focused, and self-aware, exercising excellent judgment on when to seek guidance.
  • Consistently advocates for and supports organizational change to positively impact the business.

Qualification And Education:

  • Proven experience managing delegated aspects of global, complex Phase I and II clinical studies.
  • Demonstrated success effectively managing a diverse portfolio of vendors and CROs.
  • Adept at identifying, assessing, and proactively mitigating operational risks using quantitative and qualitative data.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 10516350
  • Position Id: CA_GCTL_0605
  • Posted 7 hours ago
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