serp_jobs.filters_job_card.part_time Editor serp_jobs.h1.location_city

A company is looking for an Editor I to support the IRB Services department in reviewing submissions and preparing informed consent forms for human subject research. Key Responsibilities Conduct pre-reviews of consent forms for regulatory compliance and adherence to document standards Edit consent forms and apply sponsor language as required by client agreements Collaborate with stakeholders and stay updated on regulations and guidelines related to human subject protections Required Qualifications Minimum of 2 years of experience in technical or medical writing and / or editing Associate degree is preferred Completion of standard Human Subjects Research Training, such as CITI Ability to attend IRB meetings and complete organizational training as required Familiarity with U.S. and / or Canadian regulations in human subject research