PHARMAFull-time
Clinical Trial Associate
By Admin · Clinical Research & Clinical Operations
CHENNAI (IN)HYBRIDPOSTED: 8/27/2026
PHARMAFull-time
HIRING ORGANIZATIONICONContract Research Organization (CRO) / Clinical Research / Healthcare Services
ROLE DEFINITION & RESPONSIBILITIES
Role Overview
Full-time Clinical Trial Associate position based in Chennai, India, with an Office With Flex working arrangement.
The posting body refers to the role as Clinical Trial Administrator and describes responsibilities supporting clinical trial coordination and administration.
ICON is a global healthcare intelligence and clinical research organisation focused on accelerating the development of medicines and treatments.
Core Responsibilities
Assist with coordination and administration of clinical trials.
Ensure trial activities comply with approved protocols and regulatory requirements.
Maintain and organize clinical trial documentation, including study files and essential documents.
Support regulatory submissions and associated documentation.
Assist with preparation of study-related materials, including informed consent forms and case report forms.
Work with cross-functional teams to facilitate communication and support smooth clinical trial execution.
Track and report clinical trial metrics and milestones.
Clinical Research & Regulatory Standards
Apply knowledge of clinical trial processes, regulations, and guidelines.
Support protocol-compliant clinical trial administration.
Maintain accurate, organized, and complete study documentation.
Support regulatory documentation and submission activities.
Maintain close attention to detail throughout trial administration and documentation activities.
Collaboration & Operational Skills
Work collaboratively with cross-functional clinical research teams.
Facilitate effective communication between stakeholders involved in trial execution.
Operate effectively in a fast-paced environment.
Maintain strong organization and accuracy while supporting multiple trial activities.
Required Qualifications
Bachelor's degree in a scientific or healthcare-related field.
Prior clinical research experience or a strong interest in clinical research.
Knowledge of clinical trial processes, regulations, and guidelines.
Excellent organizational skills.
Excellent communication skills.
Ability to work collaboratively.
Strong attention to detail.
Rewards & Benefits
ICON describes its total rewards package as competitive and comprehensive, supporting health, wellbeing, and career development.
Benefits may include competitive base salary and performance-related incentives.
Health and wellbeing programmes may include medical, dental, and vision coverage where applicable.
Retirement and pension plans may be available depending on role and location.
Life assurance and disability coverage may be provided.
Employee assistance programmes and wellbeing resources may be available.
Learning and development opportunities include structured training and career pathways.
Benefits vary by role and location.
Inclusion & Accessibility
ICON is an equal opportunity employer committed to an inclusive and accessible workplace.
Reasonable accommodations are available during recruitment where required.
Applicants must have the legal right to work in the country where the position is based.
REQUIRED VERIFIED SKILLS
Clinical Trial Coordination
Clinical Trial Administration
Clinical Research
Clinical Trial Documentation
Essential Documents
Regulatory Submissions
Clinical Trial Protocols
Informed Consent Forms
Case Report Forms
Clinical Trial Metrics
Clinical Trial Milestones
Clinical Research Regulations
Clinical Research Guidelines
Organizational Skills
Communication Skills
Attention to Detail
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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