Research & Development Internship Program At Lilly

Qualifications

Skillsets required/ Additional Preferences:

• Effective teamwork skills; able to adapt to diverse interpersonal styles and leadership skills
• Exceptional verbal, written communication, and presentation skills.
• Demonstrated strength in logical thought, problem solving ability and critical thinking.
• Ability and experience in building consensus and resolving conflict to drive progress.
• Strong attention to detail & Ability to prioritize projects. Flexibility in approach and/or high learning agility
• High proficiency in Microsoft Office and Adobe Acrobat applications, with the ability to learn and use new software/technology.
• Ability to manage multiple tasks simultaneously.
• Excellent analytical skills

Takeaways from the role for the candidate:

• Subject Matter Expert knowledge within assigned Clinical Trial Operations (eTMF, Monitoring Oversight) and System’s Function
• Learn planning and execution of product lifecycle using available platforms (document management system, MS Teams, SharePoint)
• Stakeholder management and work prioritization
• Leverage technical and regulatory expertise for better results in day-to-day deliverables.

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.