IRB Specialist II - RI Scientific

Nationwide Children's Hospital•Columbus, OH

9d•Onsite

About The Position

Performs administrative functions within regulatory committees at The Abigail Wexner Research Institute (AWRI). Handles and maintains protocol submissions in a manner consistent with all federal, state, and local regulations. Ensures research activities are conducted in an ethical manner that protects the safety, rights, and welfare of participants.

Requirements

Bachelor’s Degree, required.
Three years of relevant research regulatory experience, required.
Ability to analyze and apply Federal, industry regulatory agencies and AWRI’s policies.
Effective verbal and written communication.
Working knowledge of research terminology.
Ability to work both independently and in a team-oriented environment, under minimal direction.
Proficiency with MS Office.

Nice To Haves

Master’s Degree, preferred.
Relevant certification, preferred.

Responsibilities

Provides protocol submission related technical & administrative support to Principle Investigators (PIs).
Coordinates across the organization and with multiple levels of faculty and staff to support the assembly, submission, review, and maintenance of regulatory protocols.
Serves as the primary resource for investigators regarding the organizational review requirements for research protocols.
Tracks pending applications and advises PIs on the status of submissions.
Identifies and tracks approved research protocols, including implementing procedures to assist investigators in complying with conditions imposed by the regulatory committees.
Maintains communication with PIs regarding approaching expirations of study approvals, delinquent responses, incomplete submissions, and other concerns.
Serves as super-user for the eTRAC system and contributes to the design and implementation of process improvements and business flow changes.
Provides training to PIs and staff regarding the use of the eTRAC system to submit new protocols or amend existing protocols.
Collaborates cross-functionally to ensure that researchers have completed mandatory training.
Attends and supports meetings, seminars, conferences, and workshops.
Submits minutes of meetings and drafts correspondence based on committee deliberations.
Issues approval notices based on conditions imposed by the committee.
Coordinates filing of institutional accreditation applications.
Maintains records for inspections.
Ensure the quality, content, and format of regulatory submissions to state, federal, and international agencies.
Contributes to the compliance management process and ensures timely completion of non-compliance reporting as required by federal and institutional regulatory agencies.
Attends regulatory professional meetings and identifies new or modified regulations.