Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Associate -Clinical Trial Registry Writing

Lilly
Lilly
2+ years
Not Disclosed
10 Oct. 8, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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

  • Global healthcare leader headquartered in Indianapolis, Indiana

  • Focused on discovering and delivering life-changing medicines

  • Emphasizes philanthropy, volunteerism, and putting people first


🎯 Role Purpose

  • Support the development and implementation of Clinical Trial Registry (CTR) systems and processes

  • Ensure global transparency regulations and requirements are implemented

  • Collaborate with cross-functional, multidisciplinary teams to ensure accurate and timely posting of clinical trial protocol information and study results


🧪 Key Responsibilities

Clinical Trial Registry and Results

  • Develop, maintain, and implement policies and procedures for CTR and results database workflows

  • Identify studies requiring registry and results postings, and notify responsible teams of deadlines

  • Collaborate with biostatistics, medical, and clinical trial management teams to obtain necessary data

  • Manage access rights to CTR systems

  • Serve as subject matter expert on CTR database requirements

  • Develop and deliver education and training to internal teams

  • Define and monitor metrics to support compliance

  • Stay updated on CTR regulations and guidelines

  • Exhibit flexibility to work across therapeutic areas and compounds

Project Management / Influence / Knowledge Sharing

  • Support CTR systems and processes to ensure consistent global practices

  • Provide input to deliver innovative solutions and prevent recurring issues

  • Escalate issues timely and appropriately

  • Evaluate and communicate CTR process changes

  • Share key learnings to drive simplification and replicate best practices


🎓 Basic Requirements

  • Bachelor’s degree in a scientific, health, communications, or technology field
    Or a Bachelor’s degree in any field with 2+ years of clinical development experience

  • High-level proficiency in MS Office (Word, Excel, PowerPoint, etc.)

  • Excellent written and spoken English


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 skills

  • Project and time management capabilities

  • Ability to work independently and in teams, take initiative, and follow through

  • Comfortable with ambiguity and managing conflicting priorities

  • Experience working across medical, regulatory, and legal functions

  • Strong interpersonal, negotiation, and influence skills

  • Broad knowledge of medical research processes throughout all development phases

  • Ability to work across cultures and time zones

  • Willingness to travel as required


💰 Compensation & Benefits

  • Actual compensation depends on education, experience, skills, and location

  • Eligible for company bonus and benefits


🔖 #WeAreLilly

  • Equal Opportunity Employer

  • Accommodations available for individuals with disabilities