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Transparency Specialist - Document Anonymization

Gsk Plc
GSK plc
6-9 years
Not Disclosed
Bengaluru, India
10 March 19, 2026
Job Description
Job Type: Full Time Education: M.Sc./M.Pharm/PhD 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

Transparency Specialist - Document Anonymization

Company: GlaxoSmithKline (GSK)
Location: Bengaluru, India
Job Type: Full-Time
Experience: 6–9 Years
Qualification: Master’s Degree (Life Sciences / Pharmacy / Clinical Research)


Job Overview

This is a clinical data transparency and anonymization role where you lead the preparation, anonymization, and review of clinical trial documents to ensure regulatory compliance and ethical data sharing.

You will work with cross-functional teams and external vendors to manage anonymization processes and ensure timely delivery of high-quality clinical documents.


Key Responsibilities

Document Anonymization & Compliance

Handle anonymization of clinical documents as per regulatory guidelines like EMA Policy 0070 and Health Canada PRCI

Ensure removal of PII (Personally Identifiable Information) and CCI (Commercially Confidential Information)

Maintain compliance with global regulatory requirements


Process Management & Strategy

Lead anonymization operations and ensure timelines and quality standards are met

Develop and improve anonymization processes and SOPs

Monitor industry trends and implement best practices


Stakeholder & Vendor Management

Coordinate with internal teams and external vendors

Ensure quality delivery and alignment with business expectations

Act as SME for document anonymization


Quality & Documentation

Maintain proper documentation for audits and inspections

Ensure adherence to SOPs, regulatory standards, and internal policies

Support continuous improvement initiatives


Required Skills

Clinical trial lifecycle understanding

Document anonymization & regulatory knowledge

Stakeholder management

Attention to detail

Communication & collaboration

Process improvement mindset