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
Job Summary
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.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.
Matching Summary
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.
Skills & Requirements
Must-have
Informed Consent Form (ICF) review
ICF creation experience
ICH/GCP guidelines
country regulations
Ethics Committee (EC) queries
Institutional Review Board (IRB) queries
Competent Authority (CA) queries
Nice-to-have
Protocol interpreting and review
Subject Matter Expert (SME)
Mentoring and coaching new hires
Representing department at audits
Key Requirements
4 to 8 years of experience
Minimum 2 years of ICF writing/development
Strong English writing and communication skills
Proficient knowledge of ICH/GCP guidelines
Proficient knowledge of applicable country regulations