GPS Case Management Medical Review Therapeutic Area Leader
BioSpace · Indianapolis, IN · 1 wk ago
Healthcare$156k–$229k/yrFull-time
About the role
Lilly seeks a leader in Medical Review Supervision to oversee Case Management Medical Review personnel globally, focusing on safety evaluations and fostering a collaborative environment.
Responsibilities
- Supervise Case Management Medical Review personnel across the global team, including physicians and scientists.
- Recruit, develop, and retain staff to build deep expertise in regulatory and technical areas.
- Facilitate, train, and mentor Case Management Medical Reviewers in their roles.
- Provide feedback, coaching, and support for professional growth and recognition.
- Oversee the medical evaluation of safety for Individual Case Safety Reports for all assigned compounds throughout their lifecycle.
- Develop, maintain, and share medical knowledge and expertise in the therapeutic area.
- Influence scientific and process improvements to drive change within the organization.
- Lead and participate in process improvement and innovation projects.
- Manage resources to meet business objectives and future needs.
- Collaborate cross-functionally to align goals and adjust strategies as needed.
- Partner with global GPS partners for efficient resource management.
- Act as a representative for the Lilly Case Management Medical Review team, interacting with internal and external customers.
- Collaborate with Affiliates, Business Units, and Clinical Development teams on relevant medical review expertise.
- Manage and address safety issues in collaboration with global teams.
- Understand and fulfill the roles and responsibilities of the EU Qualified Person (QP).
Requirements
- Bachelor's degree in a health-related or scientific field with 7 years of experience in the pharmaceutical industry, including direct clinical trial experience or relevant experience in drug discovery or development.
- Experience in the drug development process.
Additional Preferences
- Advanced medical-related graduate degree such as DVM, PharmD, PhD, MSN with advanced clinical specialty (e.g., Clinical Nurse Specialist/Nurse Practitioner) and 1-3 years' experience in related scientific fields.
- Knowledge of the drug development process.
- Fluent in English with highly effective written and verbal communication skills.
- Strong clinical and diagnostic skills.
- Excellent interpersonal, organizational, and negotiation skills.
- Ability to work on multiple projects and adapt to rapid task shifts.
- Ability to influence others to create a positive work environment.
- Excellent teamwork skills.
- Willingness to travel domestically and internationally as necessary.
Benefits
The position offers a competitive salary range of $156,000 - $228,800, along with a comprehensive benefits package including:
- 401(k) eligibility
- Pension plan
- Vacation benefits
- Medical, dental, vision, and prescription drug coverage
- Flexible benefits (healthcare and dependent care FSA)
- Life insurance and death benefits
- Time off and leave of absence benefits
- Well-being benefits (employee assistance program, fitness benefits, and employee clubs and activities)
Lilly is committed to creating an inclusive workplace and offers various employee resource groups (ERGs) to support diverse backgrounds and experiences.