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Associate -Clinical Trial Registry Writing

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