POL-HB-CTAAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a cooperative environment where your work contributes to the development of treatments that benefit patients worldwide.
As a Clinical Trial Associate at ICON, you will assist with the design and analysis of clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
What You Will Do:
We are currently seeking a Clinical Trial Associate to join our diverse and dynamic team. Working as a Clinical Study Associate, exclusively assigned to a Pharmaceutical Company, you will perform tasks related to the planning and execution of clinical studies.
Key responsibilities include:
• Provide support for critical day-to-day clinical study activities, including regulatory inspection readiness,
in accordance with established protocols under the general supervision of the Functional Service Provider (FSP) Manager and in collaboration with FSP CTA Manager(s)
• Collaborate with Clinical Operations/Study Manager, study teams, and Clinical Research Organizations (CROs) to support clinical study activities as defined by the clinical trial operating model
• Perform departmental tasks as needed
Accountabilities:
• Review of study documentation, including essential document packets, study plans, informed consent forms
• Supporting/oversight of risk-based monitoring
• Attendance of key team meetings as required, including Minutes for selected studies
• Supporting regulatory inspection readiness (e.g. SOP Lists, storyboard collation)
• Support clinical trial systems (e.g. CTMS/TMF) and associated activities for selected studies
• Supporting vendor contract administration as required
• Support study close-out activities, e.g. financial reconciliation
• Supporting additional ad-hoc acti
📌 Clinical Study Associate (Chennai)
🏢 ICON
📍 Chennai