Exciting Opportunity for Clinical Trial Associate at ICON

Jobs On The Way; Chennai District; On-site; INR 550,000 - 750,000; Full time

Job summary

ICON plc in Chennai, India, is seeking a Clinical Trial Associate to join our dynamic team. You will support coordination of clinical trials, ensure regulatory compliance, and contribute to the advancement of innovative therapies.

The role requires a science/healthcare degree, strong interest in clinical research, and proficiency with MS Office, especially Excel. You will work with cross-functional teams and maintain essential study documentation.

Qualifications

• Bachelor’s degree in a scientific or healthcare-related field.
• Prior experience or strong interest in clinical research.
• Knowledge of clinical trial processes, regulations, and guidelines.
• Excellent organizational and communication skills; ability to work collaboratively in a fast-paced environment.

Responsibilities

• Coordinate and administer clinical trials in compliance with protocols.
• Maintain and organize trial documentation and regulatory submissions.
• Prepare study materials such as informed consent forms and case report forms.
• Collaborate with cross-functional teams to facilitate trial execution.
• Track and report clinical trial metrics and milestones.

Skills

Organizational skills

Communication skills

Teamwork

Education

Bachelor’s degree in science/healthcare

Tools

MS Office Suite

Excel

Job description

Are you a motivated and detail-oriented individual looking for a career in clinical research? ICON plc is hiring a Clinical Trial Associate to join their dynamic team in Chennai, India. This is a great opportunity to work with a world-leading healthcare intelligence and clinical research organization and contribute to the advancement of innovative treatments and therapies.

About ICON

ICON plc is a global leader in healthcare intelligence and clinical research, providing innovative solutions and services to the pharmaceutical, biotechnology, and medical device industries. With a mission to shape the future of clinical development, ICON fosters an inclusive environment that drives innovation and excellence.

Job Responsibilities

• Clinical Trial Coordination: Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
• Documentation: Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
• Study Materials: Support the preparation of study-related materials, such as informed consent forms and case report forms.
• Collaboration: Work with cross-functional teams to facilitate communication and ensure smooth trial execution.
• Metrics and Reporting: Contribute to the tracking and reporting of clinical trial metrics and milestones.

Requirements

• Education: Bachelor’s degree in a scientific or healthcare-related field.
• Experience: Prior experience or strong interest in clinical research.
• Knowledge: Knowledge of clinical trial processes, regulations, and guidelines.
• Skills: Excellent organizational and communication skills, ability to work collaboratively in a fast-paced environment.
• Technical Skills: Highly proficient in MS Office Suite, with strong capability in Excel.

What We Offer

• Competitive Salary: A competitive salary package.
• Annual Leave: Various annual leave entitlements.
• Health Insurance: A range of health insurance offerings to suit you and your family’s needs.
• Retirement Planning: Competitive retirement planning offerings to maximize savings.
• Employee Assistance Program: Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of independent specialized professionals.
• Life Assurance: Life assurance benefits.
• Optional Benefits: Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, and more.

Why ICON?

• Diverse Culture: A diverse culture that rewards high performance and nurtures talent.
• Career Growth: Opportunities for career growth and professional development.
• Inclusive Environment: An inclusive environment that drives innovation and excellence.
• Tailor Your Resume: Make sure your resume highlights your relevant experience and skills.
• Show Enthusiasm: Demonstrate your passion for clinical research and your ability to work in a team.
• Be Prepared: Be prepared to discuss your experience and qualifications.

Don’t miss this opportunity to join ICON and contribute to the advancement of innovative treatments and therapies.