Position Title: Associate – Clinical Trial Registry Writing
Job ID: R-94166
Category: Research & Development
Job Type: Full Time, Regular
Location: Bangalore, Karnataka, India
🌍 About Lilly
At Lilly, we unite caring with discovery to make life better for people worldwide. Headquartered in Indianapolis, Indiana, Lilly is a global healthcare leader committed to:
Delivering life-changing medicines
Improving disease understanding and management
Supporting communities through philanthropy and volunteerism
We seek individuals who are dedicated to improving lives globally and contributing to a culture of excellence and collaboration.
🎯 Role Purpose
The Associate – Clinical Trial Registry (CTR) Writing supports the development and implementation of CTR systems and processes. The role ensures:
Compliance with global transparency regulations
Accurate and timely posting of clinical trial protocols and results
Coordination across cross-functional, multidisciplinary teams globally
🧠 Key Responsibilities
1. Clinical Trial Registry & Results Management
Develop, maintain, and implement policies/procedures for CTR processes and workflows.
Identify studies requiring registry and results postings and ensure timelines are communicated.
Collaborate with biostatistics, medical, clinical operations, and other functions to gather data for CTR entries.
Manage system access rights and serve as subject matter expert on CTR database requirements.
Develop and deliver training/education for internal groups.
Define and monitor metrics to ensure compliance.
Maintain and enhance knowledge of CTR regulations and guidelines.
Exhibit flexibility across therapeutic areas and compounds as needed.
2. Project Management, Influence & Knowledge Sharing
Support CTR systems and processes, ensuring consistent global practices.
Provide input to develop innovative solutions and prevent recurring issues.
Escalate issues in a timely and appropriate manner.
Evaluate and monitor CTR processes and communicate changes to relevant teams.
Share key learnings to simplify processes and replicate best practices.
🎓 Basic Requirements
Bachelor’s degree in scientific, health, communications, or technology-related field
OR Bachelor’s degree in any field with ≥2 years clinical development experience
High-level end-user computer skills (MS Word, Excel, PowerPoint)
Excellent written and verbal English skills
🛠 Additional Skills / Preferences
Experience with CTR processes and databases
Background in biostatistics, medical or regulatory writing
Strong verbal reasoning, attention to detail, critical thinking, and analytical ability
Project and time management skills
Ability to work independently and collaboratively
Experience across medical, regulatory, and legal functions
Strong interpersonal, negotiation, and influencing skills
Ability to work across cultures and time zones
Willingness to travel as required
♿ Equal Opportunity & Accommodation
Lilly is committed to inclusive workforce practices for individuals with disabilities.
For accommodations during the application process, complete the Accommodation Request Form.
Lilly is an equal opportunity employer, without discrimination based on age, race, color, religion, gender, sexual orientation, gender identity/expression, national origin, disability, veteran status, or other legally protected characteristics.
🔖 #WeAreLilly
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