Senior Global Clinical Development Trial Lead

Initial Therapeutics, Inc.

Stamford (CT)

On-site

USD 122,000 - 179,000

Full time

14 days+
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Job summary

Lilly in Stamford, CT is seeking an Associate Director, Clinical Development Trial Lead to independently lead cross-functional study teams and drive complex clinical trials globally. You will ensure trials meet quality, schedule, and budget while partnering with regional and external teams.

The role requires strategic oversight of enrollment, risk management, budget governance, and training of CDTL peers, with onsite work at Stamford, CT or Indianapolis, IN. Oncology experience is highly valued.

Qualifications

  • Bachelor's degree in a scientific or health-related field
  • 5+ years of clinical research experience or relevant field experience
  • Authorized to work in the United States full-time; Lilly does not sponsor visas
  • Onsite in Stamford, CT or Indianapolis, IN with relocation possible

Responsibilities

  • Lead cross-functional study teams to deliver trials on time, within scope and budget.
  • Develop and track global enrollment plans across geographies.
  • Manage trial budgets and monitor financials with cross-functional partners.
  • Serve as CRO contact and ensure CRO delivery of milestones.
  • Maintain Trial Master File and ensure inspection readiness.
  • Provide coaching and mentorship to other CDTLs and team members

Skills

Project management
Leadership
Cross-functional collaboration
Stakeholder influence
Communication skills
Problem solving
Travel readiness
Oncology experience

Education

Bachelor's degree

Tools

Veeva
MS Project
MS Excel
PowerBI

Job description

Lilly in Stamford, CT is seeking an Associate Director, Clinical Development Trial Lead to independently lead cross-functional study teams and drive complex clinical trials globally. You will ensure trials meet quality, schedule, and budget while partnering with regional and external teams.

The role requires strategic oversight of enrollment, risk management, budget governance, and training of CDTL peers, with onsite work at Stamford, CT or Indianapolis, IN. Oncology experience is highly valued.

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