Informed Consent Specialist

About the role

As an ICF Specialist at ICON, you'll be crucial in ensuring the accuracy, compliance, and timely approval of informed consent forms for clinical trials. Your role will directly contribute to the ethical conduct of clinical research and the successful initiation of studies.

What you'll do

• Developing and reviewing ICFs: Preparing, reviewing, and approving Subject Information Sheets (SIS) and Informed Consent Forms (ICF) for global master templates
• Be crucial in ensuring the accuracy, compliance, and timely approval of informed consent forms for clinical trials

What you need

• 4–8 yrs of experience
• Clinical research
• SOP writing
• Documentation
• Communication
• Any graduate

Good to have

• Two-wheeler