Senior Global Clinical Trial Lead – Development

Eli Lilly and Company; Stamford (CT); On-site; USD 122,000 - 179,000; Full time

Job summary

Lilly is seeking an Associate Director, Clinical Development Trial Lead (CDTL) to lead cross-functional study teams in complex clinical trials, with accountability regionally and globally. This is an on-site role based in Stamford, CT ( Indianapolis relocation optional ).

You will drive trial strategy, enrollment plans, risk management, and budget oversight, ensuring quality, on-time delivery and adherence to GCP and Lilly standards.

Qualifications

• Bachelor's degree (scientific or health-related field) preferred.
• 5+ years clinical research experience or relevant scientific/health experience.
• Authorized to work in the United States on a full-time basis.
• On-site required in Stamford, CT or Indianapolis, IN.

Responsibilities

• Lead cross-functional study teams for complex trials.
• Develop and execute regional/global trial plans and budgets.
• Assess risks and ensure regulatory compliance and quality.
• Coach CDTLs and collaborate with CROs and vendors.
• Ensure trial master file readiness and inspection readiness.

Skills

Clinical trial management

Project management

Cross-functional leadership

Regulatory knowledge

GCP/quality assurance

Education

Bachelor's degree in science/health

Tools

Veeva

MS Excel

MS Project

PowerBI

Job description

Lilly is seeking an Associate Director, Clinical Development Trial Lead (CDTL) to lead cross-functional study teams in complex clinical trials, with accountability regionally and globally. This is an on-site role based in Stamford, CT ( Indianapolis relocation optional ).

You will drive trial strategy, enrollment plans, risk management, and budget oversight, ensuring quality, on-time delivery and adherence to GCP and Lilly standards.