Job Title: Medical QC Editor (Clinical Research)
Location: Bangalore, India (Remote)
Job Type: Full-Time
Job ID: 26448
Posted: 3 Days Ago
Application Deadline: February 15, 2026
Job Category: Medical Writing / Quality Control / Clinical Research / Pharmacovigilance
Job Overview
We are seeking an experienced Medical QC Editor to review and quality-check clinical and regulatory documents within a clinical research environment. This role focuses on ensuring accuracy, consistency, regulatory compliance, and linguistic quality across a wide range of clinical documentation.
The selected candidate will collaborate closely with medical writers and cross-functional teams to maintain high editorial standards in accordance with regulatory requirements, client specifications, and internal templates.
Experience Required
Minimum 3+ years of clinical research experience
At least 3+ years of experience at Associate Medical QC Editor level or equivalent
Proven experience reviewing clinical study documentation
Key Responsibilities
Review and quality-check the following documents for accuracy, clarity, grammar, formatting, and consistency:
Clinical Study Reports (CSRs)
Patient Safety Narratives
Appendices
Informed Consent Forms (ICFs)
Clinical Protocols and Amendments
Ensure alignment with source documents, templates, and client-specific requirements
Complete quality review checklists within defined timelines
Identify discrepancies, omissions, and errors and provide detailed feedback to medical writers
Understand project scope, deliverables, and budgeted hours for assigned tasks
Participate in staff meetings, client meetings, and project update discussions as required
Assist in updating departmental templates and documentation standards
Support continuous quality improvement initiatives
Required Qualifications
Associate degree or Bachelor’s degree (BS/BA) in a relevant discipline
Strong understanding of medical, pharmacokinetic, and statistical principles
Ability to perform basic mathematical computations
Excellent command of written and spoken English
Strong knowledge of editing standards, grammar rules, and proofreading conventions
Proficiency in Microsoft Office tools (Word, Excel, PowerPoint)
Preferred Qualifications
High level of attention to detail and accuracy
Strong organizational and time management skills
Knowledge of medical terminology
Ability to work independently in a remote environment
Work Environment
Fully remote (home-based) position
Collaborative engagement with cross-functional clinical research teams
Why Apply?
This role offers an excellent opportunity for experienced medical quality control professionals to contribute to high-impact clinical documentation and regulatory submissions. The position provides exposure to global clinical research projects while maintaining flexibility in a remote working environment.
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