Eli Lilly and Company Internship | Clinical Trial Master File | Intern-TMF in Bangalore

Eli Lilly and Company Internship | Clinical Trial Master File | Intern-TMF

Eli Lilly and Company is offering an exceptional internship opportunity as an Intern-TMF in Bangalore, Karnataka. This role focuses on clinical trial operations and system functionality, providing hands-on experience in Good Clinical Practice (GCP) and cutting-edge clinical systems.

Eli Lilly and Company Recruitment Notification

About Eli Lilly and Company

Eli Lilly and Company is a global healthcare leader committed to improving lives through innovative medicines and transformative research. Headquartered in Indianapolis, Indiana, Eli Lilly combines compassionate care with groundbreaking discovery to tackle the most pressing healthcare challenges worldwide.

Internship Role: Intern-TMF

Primary responsibilities for System’s Function:

•  The role requires candidates to work on various clinical systems used across CDDA (Clinical Design, Delivery, and Analytics) and other functions in Clinical trial Foundation (CTF)
• Manage user access to relevant systems ensuring that users have met the access requirements
• Use Service now to receive and document issues (INCs) and requests and actions taken.
• Understand and respond to customer feedback on systems.
• Develop and maintain metrics as needed.
• Provide as needed support for the timely installation of new releases and patches by providing technical expertise, associated training, and business process development.
• Resolve system issues quickly to ensure continued access; apply root cause analysis as needed.

Primary responsibilities of Clinical Trial Operations:

• Knowledge of Good Clinical Practice (GCP), Good Documentation practice (GDP), Understanding of regulatory framework and other relevant regulations and guidelines.
• Understand drug discovery and development, clinical trial phases, study design, & protocols
• Understand & Support in clinical trial operations and process management.
• Conduct quality checks to ensure data integrity and support issue resolution.
• Provide administrative support to the clinical operations team and develop and maintain metrics as needed.
• Collate output from multiple data sources and conduct qualitative review.
• Assist with various tasks and projects to support the cross-functional team as needed.
• Participate in training, stay updated on industry trends, troubleshoot technical issues, and provide user support.

Key Skills and Preferences

• Strong analytical and problem-solving abilities.
• High proficiency in Microsoft Office, Adobe Acrobat, and other clinical platforms.
• Exceptional communication and interpersonal skills for effective collaboration.
• Ability to manage multiple tasks with attention to detail and adaptability.
• Prior experience or understanding of clinical trials, regulatory frameworks, and study designs is preferred.

Qualifications

• Bachelor’s or Master’s degree in Life Sciences, Pharmacy, or related fields.
• Familiarity with clinical trial management systems, eTMF, and monitoring oversight.
• Demonstrated ability to prioritize projects and work in a cross-functional environment.

Work Location

• Bangalore, Karnataka, India

How to Apply

Interested candidates can apply through the official Eli Lilly career portal. Visit: Eli Lilly Careers.

Tagged as: Global Pharma Jobs, Good Clinical Practice (GCP), Pharmaceutical Careers, Pharmaceutical Jobs