Eli Lilly and Company is a global healthcare leader headquartered in Indianapolis, Indiana, dedicated to making life better for people worldwide. The company focuses on discovering life-changing medicines, improving disease management, and contributing to communities through philanthropy and volunteerism. With a strong commitment to innovation and patient care, Lilly offers a dynamic work environment where employees can grow professionally while making a meaningful impact.
1. Job Opening: Associate/Sr. Associate – Safety Data Sciences (Job ID: R-83844)
Job Description
Eli Lilly is seeking a Safety Data Sciences Associate/Sr. Associate to join their Global Patient Safety (GPS) team in Bangalore. This role involves managing safety data systems, ensuring compliance, and supporting pharmacovigilance operations.
Key Responsibilities:
✔ System Development & Maintenance (40%)
- Develop and maintain GPS systems, tools, and technologies.
- Manage data migration, system configurations, and validation processes.
- Act as a Subject Matter Expert (SME) for GPS system activities.
✔ Safety Reporting (30%)
- Generate ad-hoc and standard safety reports using data visualization tools.
- Ensure accuracy and compliance in safety data reporting.
✔ Operational Excellence (20%)
- Identify process improvements and automation opportunities.
- Collaborate with cross-functional teams to enhance GPS analytics.
✔ Compliance (10%)
- Provide validated reports for audits and inspections.
- Ensure adherence to regulatory guidelines (FDA, ICH, GCP).
Qualifications & Skills:
- Education: Master’s/Bachelor’s degree in Health Sciences, Mathematics, Statistics, or Computer Science.
- Experience:
- Knowledge of pharmacovigilance and clinical research.
- Proficiency in data tools (Excel, Power BI, Business Objects).
- Experience in a regulated pharmaceutical environment.
- Skills: Strong analytical, communication, and leadership abilities.
2. Job Opening: Associate/Sr. Associate – Clinical Data Management (Job ID: R-82214)
Job Description
Eli Lilly is hiring a Clinical Data Management (CDM) Associate/Sr. Associate to oversee clinical trial data processes, ensuring quality and compliance.
Key Responsibilities:
✔ Portfolio Strategy & Delivery
- Manage end-to-end clinical data processes (study setup, execution, dataset delivery).
- Ensure data integrity, validation, and compliance with regulatory standards.
✔ Project Management
- Coordinate with vendors for data acquisition and database design.
- Track study metrics and ensure timely data deliverables.
✔ Enterprise Leadership
- Improve data management processes for efficiency.
- Represent Data & Analytics in cross-functional projects.
Qualifications & Skills:
- Education: Bachelor’s degree in Life Sciences, Informatics, Pharmacy, or related fields.
- Experience: 3-7 years in Clinical Data Management.
- Skills:
- Knowledge of clinical trial data standards (CDISC, SDTM).
- Familiarity with regulatory requirements (FDA, ICH-GCP).
- Strong project management and problem-solving skills.
