Clinical Research Physician (R9-R10)

Lilly • Indianapolis, IN

21d • Hybrid

About The Position

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world.
Eli Lilly and Company seeks a Clinical Research Physician (R9-R10) to provide medical leadership and guidance on the safety of pharmaceutical compounds and target therapeutics. Support surveillance programs and conduct risk management planning. Review safety signal data and liaise with scientific and business leadership. Review pharmaceutical safety reports and advise business on implications. Ensure full cooperation and high-quality medical evaluation of safety data for global regulatory purposes. Provide medical input for review of suspected adverse reactions. #LI-DNI

Requirements

• Position requires a Doctor of Medicine or Doctor of Osteopathy degree and 5 years of experience with clinical research or pharmaceutical medicine.
• 5 years of experience with pharmacovigilance and risk minimization in a regulated industry setting
• 5 years of experience with drug development processes across multiple therapeutic areas in both early and late phase clinical development
• 4 years of experience with supporting New Drug Applications, Investigational New Drug applications, and Biologics License Applications across submission stages
• 18 months of experience with clinical practice

Responsibilities

• Provide medical leadership and guidance on the safety of pharmaceutical compounds and target therapeutics.
• Support surveillance programs and conduct risk management planning.
• Review safety signal data and liaise with scientific and business leadership.
• Review pharmaceutical safety reports and advise business on implications.
• Ensure full cooperation and high-quality medical evaluation of safety data for global regulatory purposes.
• Provide medical input for review of suspected adverse reactions.

Benefits

• Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance).
• Lilly offers a comprehensive benefit program to eligible employees, including eligibility to participate in a company-sponsored 401(k); pension; vacation benefits; eligibility for medical, dental, vision and prescription drug benefits; flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts); life insurance and death benefits; certain time off and leave of absence benefits; and well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities).

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Ph.D. or professional degree
• Number of Employees: 5,001-10,000 employees