|
|
|
Index/Position No.:
229205(50%) and 255973(50%)/217250
Level 6
Position Title:
Institutional Review Board (IRB) Coordinator
Department:
Research and Sponsored Programs
Expectations for All Employees
Function of Position
This position is responsible to the Director of Human Subjects Research
Protection Program for reviewing all submissions to the Institutional Review
Board (IRB) to ensure that IRB members have all the requisite information to
review human subject research; enabling the IRB board members, including the IRB
Chairs, to perform their review tasks by providing the necessary documents and
education; acting as intercessory between the boards, researchers and other
involved institutions; and performing other related duties as assigned.
Essential Functions
-
Reviews complex scientific research protocol documents and identifies regulatory
issues and communicates those issues to Institutional Review Board (IRB) Chairs,
members and study staff with the goal of resolution.
-
Reviews all applications to the IRB, including informed consent, to
determine completeness and consistency with federal guidelines and institutional
requirements.
-
Prepares items for review by IRB Chairs, obtaining any needed information
and material.
-
Determines and compiles meeting agendas to meet distribution deadline,
disseminates meeting agendas and packets, coordinates and attends meetings.
-
Records the decision making process of the IRB in official minutes,
capturing and documenting summarization of any
controverted issues and their
resolution, clearness about the actions of the IRB and exactly what the IRB
approved, clear specification of any
modifications required to obtain approval, degree of risk, specific required
determinations, members present at the meeting, members entering and leaving the
meeting, alternate members attending and for whom they are substituting, votes
on actions, names of IRB members who abstain, names of IRB members who absent
themselves due to conflict of interest, attendance at the meeting for each
action, basis for IRB requiring change in research, basis for disapproval of
research, the rationale for significant or non-significant risk determinations,
approval periods, and other regulatory requirements.
-
Provides guidance and training to investigators and research staff
regarding procedural requirements for submission to the IRB.
-
Interfaces with other ETSU departments and other institutions, including
problem-solving at institutional levels in addition to the individual
investigator level.
-
Verifies that appropriate documentation is obtained before final IRB
approval is issued, including ensuring presence of education requirements for
all study staff, required documentation for all external performance sites, and
required documentation for investigational drug or device numbers.
-
Assists with revisions and implementation of IRB forms, Policies and
Procedures, as well as other resources for the research community.
-
Ensures that protocols undergo continuing review within current approval
period and issues expiration letters for those whose approval lapses.
-
Communicates results of IRB reviews to Principle Investigator and drafts
other correspondence as needed in an organized, clear, concise manner.
-
Interacts positively with research participants, and the research
community, and appropriately addresses issues, including complaints.
-
Maintains and audits IRB records and files.
-
Gathers information and material in response to inquiries, and responds
to requests for information regarding IRB review.
-
Leads special projects as assigned by Director.
-
Assists in identifying areas of focus for education topics and presents
workshops for the university community and affiliates on IRB Policies and
Procedures.
-
Maintains strict confidentiality.
Secondary Functions:
-
Prepares IRB annual report.
-
Maintains office filing system and databases.
-
Assists in arranging accommodations for site visitors and guest speakers.
-
Assists the Vice Provost for Research and the Director for Human Research
Subjects Protection Program as needed in review of accusation of scientific
misconduct and production and dissemination of material regarding federal
regulations and university policy regarding scientific misconduct related to
research involving human subjects.
-
Participates in required human subject training.
-
Assists with supervision of student workers.
-
Performs other related duties as assigned
Knowledge and Abilities
-
Ability to prioritize and organize multiple tasks in a detail-oriented
environment
-
Ability to guide the research community members, communicating detailed
information professionally and with brevity, both orally and in writing
-
Ability to extrapolate requirements from regulation and IRB Policies and
Procedures and provide guidance for the research community.
-
Ability to plan and present educational sessions to diverse groups of
students, faculty, staff and other constituencies
-
Ability to adapt to new, various software and applications
-
Ability to work effectively under deadlines, often in a high-pressure
environment
-
Ability to work and make decisions independently, as appropriate
-
Ability to work effectively with all university constituents and
affiliates
Supervision Given and Received
Performs under general supervision. Determines own methods of performing
assigned work.
Minimum Qualifications
Bachelor’s degree; knowledge of
human subjects regulatory compliance; exceptional computer skills including word
processing, database and presentation skills; one to two years of administrative
experience in academic research required.
May 2008
|