• Introduction
• About Eli Lilly and Company
• Internship Opportunity: Safety Management
• Primary Responsibilities
• Minimum Qualification Requirements

Internship Opportunities at Eli Lilly and Company in Pharma and Biological Science

Introduction

Eli Lilly and Company is a global healthcare leader headquartered in Indianapolis, Indiana. With a commitment to uniting caring with discovery, we strive to make life better for people around the world. Our team of 35,000 employees worldwide works diligently to discover and deliver life-changing medicines, enhance disease understanding and management, and contribute to communities through philanthropy and volunteerism. At Lilly, people are at the heart of what we do, and we’re seeking individuals who share our dedication to improving lives globally.

About Eli Lilly and Company

As a prominent player in the pharmaceutical industry, Eli Lilly and Company boasts a legacy of innovation and excellence. We focus on creating solutions that improve health outcomes and enhance quality of life. Our diverse portfolio spans across various therapeutic areas, addressing critical healthcare needs.

Internship Opportunity: Safety Management

We’re offering an exciting internship opportunity in Safety Management at our location in Bangalore, Karnataka, India. This full-time, regular position is ideal for candidates with a background in pharmaceutical and biological sciences. If you’re eager to contribute to impactful work and gain valuable experience in a global healthcare environment, this internship is the perfect platform.

Primary Responsibilities

• Utilize clinical judgment, critical thinking, and regulatory knowledge to manage adverse event data within GPS systems, ensuring data integrity, consistency, and compliance.
• Expand knowledge of Lilly compounds/products, including clinical trial design, safety profile, regulatory commitments, identified risks, adverse reactions, and risk minimization activities.
• Enhance regulatory expertise in case collection and expedited reporting requirements mandated by major regulatory agencies (e.g., FDA, EMA, MHRA, PMDA).
• Participate as a cross-functional team member of study teams as assigned.
• Contribute to system updates/enhancements and issue resolution within GPS systems.
• Process adverse events and safety information from diverse sources, ensuring thorough assessment and case completion.
• Comply with internal and external timelines for adverse event data entry.
• Lead/support literature search strategy updates and system issues/enhancements.
• Translate global/regional/local PhV regulatory requirements into expedited reporting rules and conduct related activities.
• Ensure completeness and accuracy of data management within GPS Systems and associated case management activities.

Minimum Qualification Requirements

• Bachelor’s degree or equivalent experience. Healthcare degree or study in pharmaceutical/biological science preferred.
• Strong critical thinking skills for problem-solving and decision-making, both independently and as part of a team.
• Adaptability in using electronic systems and learning new technologies.
• Basic computer skills, including word processing, spreadsheets, databases, etc.
• Effective teamwork and understanding of diversity and inclusion.
• Proficiency in English (writing, reading, speaking).

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