Clinical Trial Job at Lilly | Apply Now
Join Lilly as an Associate in Clinical Trial Registry Writing – Shape Global Healthcare. Lilly, a global leader in healthcare, is hiring an Associate for Clinical Trial Registry Writing in Bangalore. This role involves supporting clinical trial registry systems, ensuring compliance with global transparency regulations, and collaborating with multidisciplinary teams across drug development phases. If you are detail-oriented, have strong analytical skills, and are passionate about improving global healthcare, this opportunity is for you.
About Lilly
Lilly unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Employees in Jobs at Lilly work tirelessly to bring life-changing medicines to those in need, improve disease understanding and management, and contribute to communities through philanthropy. Our commitment to putting people first drives everything we do.
Job Description:
- Associate – Clinical Trial Registry Writing
- Location: Bangalore, Karnataka, India
- Category: Research & Development
- Job Type: Full Time Regular
- Job ID: R-94166
Organization Overview:
At Lilly, we unite caring with discovery to improve lives globally. Headquartered in Indianapolis, Indiana, we develop life-changing medicines, enhance disease understanding, and contribute to communities through philanthropy. Lilly employees put people first and strive to make life better for everyone.
Clinical Trial Job Overview:
The Associate, GSC Clinical Trial Registry Writing supports the development and implementation of Clinical Trial Registry (CTR) systems and processes. The role ensures global transparency regulations are applied, monitoring systems are in place, and compliance metrics are maintained. The CTR Writer collaborates with cross-functional teams across geographies and drug development phases for accurate, timely posting of clinical trial protocol information and results.
Responsibilities for the Clinical Trial Job:
Clinical Trial Registry and Results Management:
- For this Clinical Trail Job you have to develop, maintain, and implement CTR policies, procedures, and workflows.
- Identify studies for registry and results postings, ensuring timely communication with responsible functions.
- Collaborate with teams like biostats, medical, and clinical trial management to gather necessary data.
- In this Clinical Trail Job, you should manage system access rights and serve as CTR database subject matter expert.
- Provide training and define compliance metrics.
- Stay updated on CTR regulations and guidelines.
- Adapt across therapeutic areas and compounds as needed.
Project Management / Knowledge Sharing:
- For this Clinical Trial Job you should support CTR systems and ensure consistent global practices.
- Provide innovative solutions to prevent recurring issues.
- Escalate issues appropriately and monitor CTR processes.
- Share best practices to simplify processes globally.
Basic Requirements:
- Bachelor’s degree in scientific, health, communications, or technology-related field OR any field with 2+ years of clinical development experience.
- Proficient in MS Office applications.
- Strong written and spoken English skills.
Additional Skills / Preferences required for the Clinical Trial Job:
- Experience with CTR processes, databases, and regulatory/medical writing.
- Analytical thinking, attention to detail, and critical reasoning.
- Project and time management expertise.
- Ability to work independently or in teams, across cultures and time zones.
- Strong interpersonal, negotiation, and cross-functional influencing skills.
- Willingness to travel as required.
Diversity & Inclusion:
Lilly is committed to equal opportunities and providing accommodations for individuals with disabilities. We value diversity and do not discriminate based on legally protected statuses.
