Author: Lori Jennex
Date: 08-26-10 12:16
Mount Sinai School of Medicine is hiring for an IRB Analyst position in the Program for Protection of Human Subjects (PPHS) office. The person in this position will:
•Review submissions for regulatory and ethical compliance;
•Compose and distribute correspondence to investigators on behalf of the Board, Director, or Chairs;
•Prepare approval documentation in compliance with departmental policy;
•Maintain documentation and records in accordance with requirements and ensure that all records are secured and properly archived;
•Maintain computerized database for tracking purposes;
•Assist Board Manager as needed for meeting preparation;
•Take notes regarding assigned projects and postings reflective of Board meeting determinations and discussions;
•Arrange and monitor quorum at Board meetings, track IRB attendance, report significant absences under direction of the IRB Managers;
•Maintain required information about Board members for regulatory compliance;
•Coordinate the dissemination of information to Board members and the processing of responses/queries;
•Prepare agendas for Boards meetings;
•Prepare complete, high-quality, and regulatory compliant minutes from Board meetings;
•Prepare materials to distribute to Board Members or Chairs as instructed;
•Attend Board meetings, help facilitate resolution of disputed issues, assist in the preparation of minutes and post meeting communications with researchers;
•Help facilitate the orientation training and the continuing education of IRB members as instructed;
•Special projects as necessary
ABOUT MOUNT SINAI SCHOOL OF MEDICINE: Located in Manhattan, Mount Sinai School of Medicine is internationally recognized for ground-breaking clinical and basic-science research, and innovative approaches to medical education.
QUALIFICATIONS:
BA/BS; 1-2 years of experience and knowledge directly related to IRB issues and human subjects research protection or equivalent combination of experience and education (typical experience might include ethics, clinical trial performance -industry or sponsor-investigator, and/or experience in an academic health center or medical school IRB), knowledge of applicable federal regulations related to IRB and clinical research; demonstrated administrative skills; must be able to work independently with minimal supervision; excellent written and oral communications skills; excellent customer service skills. Certification as an IRB professional (CIP) is highly desirable or will be required within 12 months of employment.
To learn more, contact: Lori Jennex, Associate Director, PPHS at lori.jennex@mssm.edu.
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