Clinical Trial Associate

Roles & Responsibilities:

• Assist in coordination and administration of clinical trials as per protocol and regulatory requirements
• Maintain and organize essential clinical trial documents and study files
• Support Ethics Committee (EC) and Institutional Review Board (IRB) submissions
• Assist in preparation of study documents such as Informed Consent Forms (ICF) and Case Report Forms (CRF)
• Collaborate with cross-functional teams for smooth trial execution
• Track, monitor, and report clinical trial milestones and metrics

Qualification:

• Bachelor’s degree in a scientific or healthcare-related discipline

Experience:

• 2-4 years of clinical research experience
• Hands-on experience with CTMS
• Knowledge of NDCT rules and Indian regulatory requirements
• Experience in EC / IRB submissions

Skills:

• Strong understanding of clinical trial processes and ICH-GCP guidelines
• Excellent documentation, organizational, and communication skills
• Ability to work effectively in a fast-paced CRO environment
• Strong coordination and problem-solving abilities

About the Company:

ICON plc is a global leader in clinical research and drug development services, partnering with pharmaceutical, biotechnology, and medical device companies to bring innovative therapies to patients worldwide.