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In an era where transparency in clinical research is more important than ever, Eli Lilly and Company is leading the way with its unwavering commitment to ethical standards and patient trust. A key part of this mission involves accurate and timely disclosure of clinical trial information — and that’s where the role of a Clinical Trial Registry (CTR) Writer becomes critical.
The Role: Associate – Clinical Trial Registry Writing
Location: Bangalore, Karnataka, India
Category: Research & Development
Job ID: R-94166
Employment Type: Full-Time, Regular
As a Clinical Trial Registry Writer at Lilly, you won’t just be managing data — you’ll be ensuring that vital information about clinical trials is accessible, understandable, and in full compliance with global regulations. This role sits at the intersection of science, policy, and public health, contributing directly to the transparency that patients, healthcare providers, and regulators rely on.
Why This Role Matters
Lilly’s mission to make life better for people around the world starts with a commitment to rigorous research and responsible communication. Clinical trial registries are essential for:
- Promoting transparency in research outcomes
- Supporting informed decision-making by healthcare providers
- Reducing duplication in medical research
- Upholding public trust in the pharmaceutical industry
The Associate – CTR Writing is a vital player in achieving these goals, ensuring compliance with international regulations while contributing to a patient-centered approach to research.
Core Responsibilities
In this role, you will:
- Develop and manage processes and documentation for global clinical trial registry submissions and result disclosures.
- Collaborate across functions — including Biostatistics, Medical, and Clinical Operations — to collect and verify data required for regulatory submissions.
- Serve as a subject matter expert (SME) on registry requirements like ClinicalTrials.gov and EudraCT.
- Monitor compliance metrics, identify gaps, and drive process improvements.
- Provide training and support to internal teams on transparency regulations and registry best practices.
You’ll work across multiple therapeutic areas, often on global projects, ensuring that Lilly’s research is communicated clearly and accurately to the world.
Who Should Apply?
Ideal candidates will bring:
- A Bachelor’s degree in a scientific, medical, communications, or technical field — or in any discipline with 2+ years of clinical development experience
- Excellent English writing and communication skills
- Proven proficiency in MS Office tools
- A passion for medical research, transparency, and global health ethics
Preferred candidates may also have experience with clinical trial databases, regulatory or medical writing, or a background in biostatistics or legal compliance.
What You’ll Gain at Lilly
At Lilly, your work will make a global impact. You’ll be part of a company that:
- Values integrity, inclusion, and innovation
- Offers opportunities for career growth and cross-functional collaboration
- Supports continuous learning and upskilling in scientific communication
- Provides a global platform to influence clinical research transparency standards
You’ll also be joining a culture that puts people first—from patients to employees—driven by the belief that caring and discovery go hand in hand.
Join the Mission
If you’re detail-oriented, passionate about science, and eager to play a part in the future of ethical clinical research, this role offers the opportunity to grow your career while making a meaningful difference.
Apply today and become part of a team dedicated to improving lives through transparency, innovation, and scientific excellence.
🔗 Visit Lilly Careers to Apply
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