IRB Research Protocol Consultant

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Prior to submitting your application, please review and update (if necessary) the information in your candidate profile as it will transfer to your application. Job Title:

IRB Research Protocol Consultant

Department:

ERIK Office of Responsible Research Practices

Position Overview

The IRB Research Protocol Consultant serves as a principal liaison between the university, IRBs, senior institutional leaders, and other applicable internal and external institutional areas. The IRB Research Protocol Consultant:

Exercises sound judgment in independently monitoring research analytics to ensure screening timeliness and conformance with federal regulations and guidance, state laws, and institutional policies governing research involving human subjects under the direction of the associate director, IRB operations.

Applies ethical principles to resolve complex issues; provides guidance and oversight in the review requirements for complex research submissions; guides ORRP staff and IRB members in making regulatory determinations.

Provides professional service to the Institutional Review Board (IRB, Board) and investigators involving the application of ethical principles and concepts.

Provides convened meeting training on developing agendas and reviewer assignments, complex and technical deliberations, regulatory findings, and Board actions.

Guides protocol analysts to effectively help investigators formulate responses to IRB requests; assists researchers to secure timely IRB approvals.

Serves as a leader and subject matter expert in specific regulatory and operational areas, such as collaborative and multi-site research, research review and approval processes, overseeing the management of convened IRB meetings, or applying analytics/metrics to manage staff workflow.

Oversees the development and implementation of other human research programs.

Supervises review/training activities; monitors and prioritizes workflow, and provides metrics to set team-level targets.

Leads business process improvement initiatives and participates in development of applicable education programs; partners with colleges and departments in outreach activities; attends the Public Responsibility In Medicine & Research (PRIM&R) national conference through the conduct of workshops or poster presentations.

Oversees electronic submission system testing and makes recommendations for enhancements.

Represents ORRP at events and serves as a speaker at education and training events for university units, including the Comprehensive Cancer Center Clinical Trials Office (CCC-CTO), Center for Clinical Research Management (CCRM), College of Nursing, Clinical and Translational Science Institute, and others.

Identifies opportunities for continued ORRP staff education and/or training, providing recommendations and feedback to ORRP leadership.

Performs education and/or training as needed for junior level staff.

Participates in the development of training for senior level staff.

Manages new staff recruitment, onboarding, mentoring, and training.

Supervises junior level protocol analysts, including providing direction of daily activities, evaluating performance, and setting clear expectations on responsibilities. This search is recruiting for three openings.

Required Qualifications

Bachelor's degree or an equivalent combination of education and experience.

6 years of relevant work experience.

Experience in IRB operations.

knowledge of and experience applying regulations governing research involving human subjects.

Strong problem solving and customer service experience.

Proficient in the use of Microsoft Office suite.

Ability to work within a regulatory and deadline-driven environment;

Certified IRB Professional certification. Desired Qualifications

8-12 years of human subjects regulatory experience or relevant work experience.

Knowledge of and experience with IRB operations and research methodologies.

Experience in projects. Application Materials

A resume and cover letter are required Additional Information:

Salary

The pay range for this job profile is $75,700.00 - $98,900.00. The offer for this position will fall within this range based on multiple factors including internal equity, unit's available budget, and the candidate's qualifications

ERIK Overview

Join the Enterprise for Research, Innovation and Knowledge (ERIK) at The Ohio State University and become a part of a dynamic, forward-thinking team dedicated to pushing the boundaries of discovery and innovation. ERIK positions Ohio State to expand curiosity-driven research and creative expression, further develop our research community of faculty, staff, and students, and grow the innovation ecosystem to address big challenges and improve communities locally and globally. We are seeking passionate individuals who are committed to making a meaningful impact through collaboration, innovation, and excellence. To learn more about our mission and work, please visit

Position Mapping

Function: Research Administration

Sub-function: Research Protocol

Career Band and Level: S4 Consultant

Location:

Mount Hall (0311)

Position Type:

Regular

Scheduled Hours:

40

Shift:

First Shift

Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.

Thank you for your interest in positions at The Ohio State University and Wexner Medical Center. Once you have applied, the most updated information on the status of your application can be found by visiting the Candidate Home section of this site. Please view your submitted applications by logging in and reviewing your status. For answers to additional questions please review the frequently asked questions.

The university is an equal opportunity employer, including veterans and disability.