Editor I, Consent Form Development

This is a fully remote position, open to applicants in United States.

📋 Description

• Assists the IRB Services department with the assessment of incoming submissions and the drafting of informed consent forms (ICFs).

• Performs a thorough pre-review of new and updated consent forms to ensure compliance with regulations.

• Edits both new and revised consent forms to guarantee adherence to regulatory standards.

• Works collaboratively with Board members and staff to incorporate all necessary revisions into the consent form.

• Stays informed about U.S. and/or Canadian Regulations and Guidelines pertaining to Human Subject Protections.

• Completes standard Human Subjects Research Training, including CITI certification.

• Participates in one IRB meeting each month to deepen knowledge and understanding of IRB processes.

⛳️ Requirements

• A minimum of 2 years of experience in technical and medical writing and/or editing.

• An Associate's degree is required.

🏝️ Benefits

• Health coverage.

• Paid holidays.

• Variable bonus.