Global Clinical Development Trial Lead

BioSpace; Stamford (CT); On-site; USD 122,000 - 179,000; Full time

Job summary

Lilly in Stamford, CT seeks an Associate Director, Clinical Development Trial Lead to guide cross-functional teams through complex trials. You will shape study strategy, manage timelines, budgets, and risk, and ensure quality and regulatory compliance across regions.

You will partner with CROs, ISSTs/ASTs, and TPOs, lead enrollment planning from country allocation to LPET, and mentor new CDTLs while advancing patients' access to innovative therapies.

Qualifications

• Bachelor's degree in a scientific or health-related field is required.
• 5+ years of clinical research experience or relevant scientific/health experience.
• Authorized to work in the United States full-time; Lilly does not sponsor visas.

Responsibilities

• Lead cross-functional study teams to deliver complex clinical trials on time and within scope.
• Develop enrollment plans, monitor risks, and manage trial budgets and changes.
• Coach CDTLs and coordinate with CROs, ISSTs/ASTs, and regional partners.

Skills

Clinical leadership

Cross-functional collaboration

Project management

Regulatory knowledge (GCP)

Communication

Travel readiness

Education

Bachelor's degree (scientific/health)

Tools

MS Project

Veeva

PowerBI

MS Excel

Job description

Lilly in Stamford, CT seeks an Associate Director, Clinical Development Trial Lead to guide cross-functional teams through complex trials. You will shape study strategy, manage timelines, budgets, and risk, and ensure quality and regulatory compliance across regions.

You will partner with CROs, ISSTs/ASTs, and TPOs, lead enrollment planning from country allocation to LPET, and mentor new CDTLs while advancing patients' access to innovative therapies.