ICON is a global leader in clinical research, providing outsourced development services to pharmaceutical, biotechnology, and medical device industries. With a strong focus on innovation and patient-centric solutions, ICON supports clinical trials worldwide, helping bring new treatments to market efficiently.
Job Description
We are seeking a Clinical Trial Assistant (CTA) to join our dynamic team in Bangalore. This role is ideal for professionals with 2-3 years of experience in clinical trial coordination and site payments.
Key Responsibilities:
- Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements.
- Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions.
- Support the preparation of study-related materials such as informed consent forms and case report forms.
- Collaborate with cross-functional teams to ensure smooth trial execution.
- Track and report clinical trial metrics and milestones.
Qualifications & Skills:
- Bachelor’s degree in a scientific or healthcare-related field.
- 2-3 years of experience as a Clinical Trial Assistant supporting global sponsor-initiated studies.
- 2 years of experience in Site Payments activities.
- Knowledge of clinical trial processes, regulations (ICH-GCP), and guidelines.
- Strong organizational and communication skills.
- Ability to work in a fast-paced environment with attention to detail.
Why Join ICON?
ICON offers a competitive salary and a comprehensive benefits package, including:
- Health insurance for you and your family.
- Retirement planning and life assurance.
- Flexible leave policies and well-being programs.
- Global Employee Assistance Program (EAP)Â for mental health support.
- Additional perks like childcare vouchers, gym discounts, and more.
How to Apply
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