Lilly, a global healthcare leader headquartered in Indianapolis, Indiana, is dedicated to making life better for people worldwide. With a legacy of groundbreaking medical innovations, Lilly focuses on improving disease understanding, management, and community well-being through philanthropy and volunteerism. As part of its commitment to fostering talent, Lilly offers roles like the Intern-TMF position in Bangalore, Karnataka, providing hands-on experience in clinical trial operations and system management.
Key Responsibilities
System’s Function
- Manage and grant user access across Clinical Design, Delivery, and Analytics (CDDA) systems.
- Utilize ServiceNow for issue documentation, resolution, and request tracking.
- Address user feedback and resolve system issues swiftly, applying root cause analysis.
- Support the installation of new software releases and patches, ensuring seamless system upgrades.
- Maintain and develop relevant metrics to enhance system functionality.
Clinical Trial Operations
- Understand Good Clinical Practice (GCP) and Good Documentation Practice (GDP).
- Gain insights into clinical trial phases, study design, and protocols.
- Support operations and process management in clinical trials.
- Conduct quality checks to ensure data integrity and issue resolution.
- Provide administrative and project support to cross-functional clinical teams.
- Review and collate data outputs, ensuring alignment with trial requirements.
Required Skills and Qualifications
Skillset
- Strong teamwork and adaptability to diverse interpersonal styles.
- Excellent verbal, written communication, and presentation skills.
- Proficiency in logical problem-solving and critical thinking.
- Strong attention to detail and multitasking capabilities.
- Advanced knowledge of Microsoft Office and Adobe Acrobat applications.
Preferred Qualities
- Ability to prioritize and manage multiple tasks.
- Flexibility and high learning agility.
- Proven analytical skills and a proactive approach to resolving issues.
Learning and Takeaways
- Gain expertise in Clinical Trial Operations such as eTMF and Monitoring Oversight.
- Hands-on experience with platforms like document management systems, SharePoint, and MS Teams.
- Develop skills in stakeholder management and project prioritization.
- Enhance technical and regulatory expertise for impactful results.
