Global Clinical Trial Lead – Development & Strategy

BioSpace; Indianapolis (IN); On-site; USD 65,000 - 149,000; Full time

Benefits offered by this job

Company bonus

401(k) plan

Health benefits

Job summary

Lilly in Indianapolis seeks a Clinical Development Trial Lead Associate to guide cross-functional study teams in executing complex trials with quality and on time delivery. You will apply project management, regional knowledge, and scientific expertise to coordinate efforts and meet trial deliverables across regions.

The role emphasizes collaboration with investigators, ISSTs/ASTs, and TPOs, with responsibility for enrollment strategy and global risk mitigation, while ensuring regulatory and

Qualifications

• Bachelor’s degree in a scientific or health-related field.
• 3 years clinical research experience or relevant clinical trial experience; or an advanced degree.
• Authorized to work in the United States on a full-time basis; Lilly does not sponsor work visas.

Responsibilities

• Lead cross-functional study teams to deliver trials on time and within scope.
• Develop global milestones and monitor timelines across geographies.
• Assess and mitigate trial-level risks with input from science, trials, and regional experts.
• Coordinate Investigator Study Specific Training and Investigator Engagement Meetings.
• Manage enrollment strategy from country allocation through Last Patient Entered Treatment (LPET).
• Serve as single point of contact for trial communications with study teams and vendors.

Skills

Immunology experience

Trial execution knowledge

Cross-cultural collaboration

Influence without authority

Leadership and networking

Effective communication

Problem solving

Adaptability

Education

Bachelor's degree (scientific or health-related)

Job description

Lilly in Indianapolis seeks a Clinical Development Trial Lead Associate to guide cross-functional study teams in executing complex trials with quality and on time delivery. You will apply project management, regional knowledge, and scientific expertise to coordinate efforts and meet trial deliverables across regions.

The role emphasizes collaboration with investigators, ISSTs/ASTs, and TPOs, with responsibility for enrollment strategy and global risk mitigation, while ensuring regulatory and