Job Details
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Job Title: Clinical Research Monitor - CTSI
Department: Health Sciences | Clinical and Translational Science Institute
The Ohio State Clinical and Translation Science Institute (CTSI) Research Monitor serves, upon sponsor request, as an independent oversight agent for clinical research trials to ensure the protection of participant safety, data integrity, and regulatory compliance. The monitor is responsible for monitoring the conduct of clinical research trials to ensure trials are conducted, recorded, and reported in accordance with protocol, US Food and Drug Administration (FDA) regulations, Good Clinical Practice (GCP), applicable regulatory requirements, and Standard Operating Procedures (SOPs).
The study monitor will assess the accuracy and completeness of the study data and essential records of their assigned trials and reports findings the Sponsor-Investigator, the site PI and their applicable research staff, and other Sponsor-Investigator agents such as the DSMB, Data Manager, Statistician, Funding Agency, and Project Manager. The monitor works in conjunction with the CTSI Training Team, Data and Safety Monitoring Board (DSMB), and the Multicenter Trials Coordination Center (MTCC) and Data Coordination Center (DCC), as applicable.
The study monitor will review and provide feedback on study related documents, such as the study protocol, consent form, case report forms, and the clinical trial monitoring plan; support the study sponsor in the development of the clinical trial monitoring plan; assess adequacy of research facilities/equipment at participating sites; conduct monitoring visits to review essential records, drug/device accountability, and source verification; assess protocol adherence, adequacy of the informed consent process; and timely recording/reporting of adverse events and other promptly reportable events; issue queries to the study team regarding monitor findings and recommend necessary steps to resolve identified compliance issues; maintain detailed records of monitoring sessions and monitoring results; complete quality and/or audit checks, assist with audit preparation and serve as a liaison during regulatory inspections; maintain detailed knowledge of applicable university, state, federal, international regulations and good clinical practice guidelines; assist CTSI leadership with writing and implementing CTSI Standard Operating Procedures (SOPs); assist CTSI leadership with developing and maintaining a monitoring framework; assist with developing and presenting research related trainings; assist CTSI leadership with completing outreach to research core services and research colleges and departments; the monitor may assist CTSI Leadership with clinical trial project management related tasks, such as clinical trial reporting, monitoring trial progress, budgets, contracts, and multi-site management.
The monitor will assist the CTSI with completing regulatory submissions and obtaining regulatory approvals, monitor regulatory progress/status, maintain essential records help coordinate study related meetings, provide regulatory status updates to CTSI Leadership, the Sponsor-Investigator, the participating study sites, and other Sponsor-Investigator agents such as the Data and Safety Monitoring Board (DSMB), Data Manager, Statistician, Funding Agency, and Project Manager.
Minimum Education & Experience Required
Candidates must hold a bachelor's degree in biological sciences, health sciences, social sciences, or another medical field, or possess an equivalent combination of education and experience. A master's degree in a relevant field is desired. A minimum of 3 years of relevant experience is required, with 4-6 years preferred. Experience in a progressively responsible clinical research or administrative capacity working in clinical research required; considerable knowledge of federal regulatory requirements pertaining to research in human subjects required; considerable clinical research, regulatory, and monitoring experience strongly preferred. Clinical research certification from an accredited certifying agency is required to be considered for the position and the certification must be maintained. Requires successful completion of a background check; qualified candidates may be asked to complete a pre-employment physical, including a drug screen. Experience using various software including Microsoft office, electronic medical records, Electronic Data Capture (EDC) systems, and clinical trial management systems; considerable knowledge of OSU research policies and procedures preferred; previous monitoring experience preferred; requires successful completion of a background check; pre-employment physical including a drug screen.
MINIMUM REQUIRED QUALIFICATIONS
Bachelor's degree or equivalent experience. An advanced degree in a relevant field may be desirable. 4 years of relevant experience required. 4-8 years of relevant experience preferred.
Function: Research and Scholarship
Subfunction: Clinical Research
Band: Individual Contributor Series-Specialized
Level: S3 Senior
Additional Information:
This position may require limited travel (<10%). It will involve extended periods of reviewing documents and data. This position may work in office and research laboratory/clinical environments. This position has hybrid working opportunities.
The monitor must maintain high standards of professional conduct and confidentiality. They will build trustworthy and reliable relationships across the research enterprise while maintaining monitoring independence and high ethical standards. The monitor may identify compliance issues and will provide practical, risk-based solutions
Location: Prior Hall (0302)
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.
Organization
About The Ohio State University
The Ohio State University, one of the biggest and most comprehensive universities in the country, creates experiences that bring together expertise, ideas and resources to improve communities locally and globally.
Ohio State is regularly honored as one of the nation's top 20 public universities. With campuses and research centers throughout the state, the institution's unrivaled depth and breadth advance innovation, health care and research within Ohio's communities. For more than 150 years, Ohio State has inspired the next generation of leaders, discovering groundbreaking medical breakthroughs and finding solutions to the problems the world is facing now.
Ohio State also has a top-rated academic medical center and a premier cancer hospital and research center.
Ohio State offers more than 200 majors and programs — plus 500 specializations — for undergraduates, in addition to more than 230 master's, doctoral and professional degree programs and an estimated 12,000 course offerings.
Join Ohio State's Community
At The Ohio State University, we connect people, ideas and resources to put knowledge into practice and create meaningful impact in people's lives. Buckeyes lead with purpose. We advance excellence and inspire people to join in and take action. Together, we'll create meaningful impact at a scale few others can match.
Explore our Extensive Benefits
Ohio State provides access to opportunities and resources for all employees. Starting your first day, Ohio State offers you a comprehensive benefits package.
- WORK-LIFE: Flexible and remote work arrangements where applicable, child care program, and access to educational, athletic and cultural events.
- RETIREMENT: State pension and alternative options with competitive employer contributions, as well as optional supplemental plans.
- HEALTH: Medical, dental, vision and prescription coverage, life insurance, flexible spending accounts and wellness programming.
- TIME OFF: Paid vacation and sick time, parental and medical leave plus 11 paid holidays. Short and long-term disability options also available.
- FINANCIAL: Tuition assistance for employees and their dependents, adoption assistance, and discounts with preferred vendors and university partners.
- WELLNESS: Lifestyle spending account, employee assistance program, health reimbursement account, and employee wellness program.
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