Informed Consent Specialist

ICON plc

Bangalore, India
Icf review and creation experience
Proficient knowledge of ich/gcp guidelines
Strong english writing and communication skills
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

  • ICF review and creation experience
  • Proficient knowledge of ICH/GCP guidelines
  • Strong English writing and communication skills

Nice-to-have

  • Ability to work collaboratively
  • Strong analytical and problem-solving skills
  • Mentorship and coaching abilities

Key Requirements

  • 4 to 8 years of experience
  • Minimum 2 years of experience in ICF writing
  • Protocol interpreting & review preferred

Work Rights

Not specified

Tailored Resume

Cover Letter