PHARMAFull-time
Study Support Assistant
BANGALORE (IN)HYBRIDPOSTED: 8/13/2026
PHARMAFull-time
HIRING ORGANIZATIONICONContract Research Organization (CRO) / Clinical Research / Healthcare Services
ROLE DEFINITION & RESPONSIBILITIES
Assist in the preparation, formatting, and distribution of clinical study documents, including protocols, informed consent forms, and regulatory filings.
Coordinate study-related meetings, record meeting minutes, and track project action items.
Manage study correspondence, emails, and operational documentation in compliance with regulatory standards and internal SOPs.
Support study teams with the maintenance of clinical trial master files, documentation, and tracking of trial supplies.
REQUIRED VERIFIED SKILLS
Clinical Research
Clinical Trial Administration
Study Documentation
Regulatory Submissions
Microsoft Office
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
READY TO SUBMIT?
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