Assist with RAS research compliance, Responsible Conduct of Research, and Research Integrity web page maintenance and updates with program, policy, and resources.
November 23, 2022
Review FAS/SEAS submitted annual fCOI disclosures for 1500+ faculty and lecturers in order to determine whether there is a significant conflict that requires managing.
January 03, 2023
Communicate with research sites regarding the distribution and review of site essential documentation.
January 08, 2023
Draft proposal language and protocol guidance regarding human subject protections.
January 18, 2023
Works with the IRB staff to facilitate throughput of studies through the review process.
March 18, 2023
Provide technical support for research compliance systems (especially fCOI) to include responding to inquiries from users, testing the application prior to new releases, and reporting and following up on any bugs or enhancement requests.
March 24, 2023
Manages departmental work flow processes and activities pertaining to IRB submission, review and approval of protocols involving human subjects submitted by researchers.
April 08, 2023
Participate in University and/or school-level committees and working groups as necessary.
April 13, 2023
Stay abreast of requirements and changes in the regulatory environment and assist with interpretation and distribution of emerging MGH and Partners policies as well as local, state, and federal laws and regulations as it relates to research compliance.
April 25, 2023
Obtains and processes safety reports from both cooperative groups and pharmaceutical companies and prepares memos to Principal Investigators (PI) for review and signature.
May 19, 2023
