Informed Consent Specialist
BengaluruFull-time4–8 yrsPosted 1 week ago
Senior pharma role at ICON India Clinical - in Bengaluru. Needs 4+ years.
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
- Clinical research
- Learning and development
- SOP writing
- Documentation
- Communication