PHARMAFull-time
Medical Writer I
BANGALORE (IN)REMOTEPOSTED: 8/14/2026
PHARMAFull-time
HIRING ORGANIZATIONICONContract Research Organization (CRO) / Clinical Research / Healthcare Services
ROLE DEFINITION & RESPONSIBILITIES
Perform Trial Master File (TMF) Quality Control (QC) to ensure inspection readiness and ICH/GxP compliance.
Support clinical study report (CSR) lifecycles, narrative coordination, appendices management, and document formatting.
Conduct rigorous QC checks of regulatory documents against source data using Microsoft Word and Adobe Acrobat tools.
Maintain EndNote libraries and literature references to support ongoing medical writing deliverables.
Manage document workflows, uploads, version control, and approvals in Electronic Document Management Systems (EDMS) like Veeva Vault.
REQUIRED VERIFIED SKILLS
Medical Writing
Quality Control (QC)
Clinical Study Reports (CSR)
Veeva Vault EDMS
MS Word
Adobe Acrobat
ICH-GCP
TMF
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
ORGANIZATION CONTEXT & CULTURE
ICON plc is a global provider of outsourced drug development and commercialization services to pharmaceutical, biotechnology, medical device, and government organizations. The company specializes in a broad range of clinical research services, from Phase I-IV studies to consulting and data solutions. ICON helps its clients accelerate the development of drugs and devices through comprehensive scientific and operational expertise.
TEAM SIZE: 41,100+ employees
INDUSTRY: Contract Research Organization (CRO) / Clinical Research / Healthcare Services
RECOMMENDED TRAINING
1/5
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