Director – Case Management Medical Review
Location: Bangalore, Karnataka, India
Job Type: Full-Time, Regular
Job ID: R-98032
About Lilly
At Lilly, we unite caring with discovery to make life better for people worldwide. As a global healthcare leader headquartered in Indianapolis, Indiana, Lilly employees work to deliver life-changing medicines, improve disease understanding, and contribute to communities through philanthropy and volunteerism. We prioritize patients and strive to make meaningful contributions to healthcare globally.
Purpose of the Role
The Director – Case Management Medical Review provides strategic, technical, and leadership oversight for Case Management Medical Review within therapeutic area hubs. This role leads a global team of physicians and scientists, ensuring high-quality evaluation of safety data, development of technical expertise, and alignment with global medical, regulatory, and pharmacovigilance standards.
The Director reports to the Senior Director/Executive Director – Case Management Medical Review and partners with global leaders in Medical Review, Case Management, and Global Patient Safety (GPS).
Key Responsibilities
Medical Review Leadership
Lead a global team of Case Management Medical Review physicians and scientists within assigned therapeutic areas.
Supervise recruitment, development, mentorship, and retention of team members, fostering technical expertise.
Oversee the medical evaluation of Individual Case Safety Reports (ICSRs) across assigned compounds to inform safety profiles.
Drive process improvement, innovation, and standardization in medical review operations.
Contribute to the functional strategic plan and manage resources to meet current and future business objectives.
Collaborate cross-functionally to ensure alignment with clinical development, regulatory, and pharmacovigilance teams.
Enterprise & External Leadership
Represent Case Management Medical Review internally and externally, ensuring high-quality medical evaluation and compliance.
Build relationships with key stakeholders, including affiliates, business units, and clinical teams.
Support clarification or resolution of safety issues in collaboration with global teams.
Ensure support for EU Qualified Person (QP) responsibilities when applicable.
Compliance & Governance
Maintain compliance with local and international regulations, Good Clinical Practices (GCP), and Lilly policies.
Provide guidance and oversight to ensure medical review activities align with corporate safety standards and regulatory requirements.
Qualifications
Basic Requirements
Medical degree (MD, MBBS, or DO) with board eligibility or certification in an appropriate specialty/subspecialty.
Clinical development or pharmacovigilance experience preferred.
Knowledge of drug development and regulatory frameworks.
Fluent in English, with strong verbal and written communication skills.
Excellent clinical, diagnostic, organizational, interpersonal, and negotiation skills.
Ability to manage multiple priorities in a fast-paced, matrixed environment.
Willingness to travel domestically and internationally as required.
Preferred Attributes
Minimum 3+ years of prior people management experience.
Strong leadership skills with demonstrated ability to influence cross-functional teams.
Proven track record in mentoring, team development, and strategic planning within a medical review or pharmacovigilance function.
Why Join Lilly
Lead global pharmacovigilance and medical review initiatives that impact patient safety worldwide.
Work in a collaborative, innovative environment committed to diversity, equity, and inclusion.
Drive professional growth and leadership development in a high-impact medical affairs and safety role.
Contribute directly to patient safety, scientific excellence, and business strategy within a leading global pharmaceutical organization.
Lilly is an equal opportunity employer and provides accommodations for individuals with disabilities during the hiring process. For assistance, please visit Lilly Workplace Accommodation.
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