Job Title: Associate – Clinical Trial Registry Writing
Location: Bangalore, Karnataka, India
Category: Research & Development
Job Type: Full-Time, Regular
Job ID: R-94166
Company Overview
At Lilly, we unite caring with discovery to make life better for people around the world. Headquartered in Indianapolis, Indiana, we are a global healthcare leader focused on:
Discovering and delivering life-changing medicines
Improving the understanding and management of diseases
Giving back to communities through philanthropy and volunteerism
We value people first, and we seek individuals determined to make a meaningful impact globally.
Role Overview
The Associate, GSC Clinical Trial Registry (CTR) Writing will support the development and implementation of Clinical Trial Registry systems and processes. This role ensures compliance with global transparency regulations, accurate posting of clinical trial protocols, and study results across multiple geographies and phases of drug development.
The CTR writer will collaborate with cross-functional teams to maintain data integrity, monitor compliance, and optimize registry processes.
Key Responsibilities
Clinical Trial Registry & Results Management
Develop, maintain, and implement policies/procedures for CTR and results database processes.
Identify studies requiring registry/results postings and communicate timelines/deadlines to responsible teams.
Collaborate with biostatistics, medical, clinical trial management, and other teams to obtain required data.
Manage access rights to CTR systems as needed.
Serve as subject matter expert on CTR database requirements.
Provide education and training to internal teams.
Define and monitor metrics to support compliance.
Maintain and enhance knowledge of CTR regulations and guidelines.
Exhibit flexibility across therapeutic areas and compounds based on project assignment.
Project Management & Knowledge Sharing
Support CTR systems and processes, ensuring consistent global practices.
Provide input for innovative solutions and prevent recurring issues.
Escalate issues in a timely manner.
Evaluate CTR processes and communicate updates to relevant stakeholders.
Share key learnings to drive process simplification 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 at least 2 years of clinical development experience
High-level end-user computer skills (MS Office: Word, Excel, PowerPoint, etc.)
Mastery of English, written and spoken
Preferred Skills & Experience
Experience with CTR processes and databases
Background in biostatistics, medical writing, or regulatory writing
Strong verbal reasoning, attention to detail, critical thinking, and analytical skills
Project and time management proficiency
Ability to work independently and collaboratively in diverse environments
Experience interacting with medical, regulatory, and legal teams
Strong interpersonal, negotiation, and influencing skills
Knowledge of medical research processes across all phases of development
Ability to work across cultures and time zones
Willingness to travel as required
Equal Opportunity & Accessibility
Lilly is committed to fostering an inclusive workforce and provides accommodations for individuals with disabilities. To request accommodations during the application process, please complete the workplace accommodation form.
Lilly is an equal opportunity employer and does not discriminate based on age, race, color, religion, gender, sexual orientation, gender identity or expression, national origin, veteran status, disability, or any other legally protected status.
#WeAreLilly
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