Informed Consent Specialist

A company is looking for a Remote Contract Analyst.

Key Responsibilities

Act as the primary contact for informed consent (IC) activities related to assigned clinical studies

Ensure timely and compliant completion of the IC approval process by coordinating with stakeholders

Create and maintain accurate IC files and perform periodic audits to ensure completeness

Required Qualifications

Bachelor's degree in Clinical Research, Biology, or Chemistry

Minimum of 2 years of experience in consent / Informed Consent (IC) / contracts within clinical research

Experience in document management and following standard operating procedures

Ability to manage relationships with diverse teams and stakeholders

Familiarity with clinical processes, regulations, and compliance guidelines