Senior IRB Analyst, School of Medicine, Clinical Research
The Sr. IRB Analyst provides administrative and regulatory support for the IRB staff, the IRB Chairs, the IRB Board members and the institution’s researchers. Additionally, will be responsible for processing IRB submissions and serving as an alternate voting member on the IRB. The Sr. Analyst is designated by the IRB Chair as an Expediter to sign off on IRB expedited reviews. The IRB Chairs and Board members rely heavily on the regulatory knowledge and expertise of the Senior IRB Analysts to guide their reviews and decisions. The incumbent will work independently under the general supervision of the IRB Director.
Additional responsibilities include, but are not limited to:
Performs regulatory analysis and administrative review of IRB submissions to ensure compliance with Federal research regulations and institutional policies (including new submissions, renewals, amendments, AEs and deviations)
Maintains documentation in accordance with Federal regulations and institutional policies.
3-5 years of experience and Bachelor's degree required. Master's degree preferred.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability status, protected veteran status, or any other characteristic protected by law. We are a VEVRAA Federal Contractor.
Boston, Massachusetts, United States