Regulatory Compliance Officer Job at The Ohio State University, Columbus, OH

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  • The Ohio State University
  • Columbus, OH

Job Description

Screen reader users may encounter difficulty with this site. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions. Current Employees and Students: If you are currently employed or enrolled as a student at The Ohio State University, please log in to Workday to use the internal application process. Welcome to The Ohio State University's career site. We invite you to apply to positions of interest. In order to ensure your application is complete, you must complete the following: Ensure you have all necessary documents available when starting the application process. You can review the additional job description section on postings for documents that may be required. 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: Regulatory Compliance Officer Department: CCC | Administrative Office The Regulatory Compliance Officer assures that research protocols of the OSUCCC Clinical Trials Office (CTO) are in compliance with University, state and federal regulations; ensures timely submission of all appropriate paperwork for review by appropriate agency. Responsibilities Collaborates with investigators during study development to facilitate and confirm that appropriate regulatory safeguards have been included Conducts detailed reviews of assigned protocols and informed consent forms prior to IRB review Ensures timely submission of protocol documents for review by appropriate agency communicates with all CTO research projects sponsors (academic, federal, industry) to ensure compliance Interfaces with various internal and external entities to coordinate and effectively compile all appropriate data relevant to the conduct of a CTO trial Develops IRB submission packets for protocols, including writing of abstract, submission of standard forms and drafting of informed consent forms Provides and maintains tracking system to assess progress of a protocol's review; maintains regulatory essential files on submitted and approved studies Reviews all protocol revisions and amendments; amends consent forms if needed and follows established guidelines to determine if amendments requires IRB review Distributes all amendments and IRB approved informed consent forms to relevant university protocol holders Acts as main point of contact for the dissemination of all approved study material and works collaboratively with various internal and external departments to ensure relevant updates are communicated effectively and timely Attends meetings; serves as principal contact from CTO to regulatory agencies including FDA and IRBs Continually monitors federal and sponsor rules, regulations and processes to identify and interpret new, updated or changed requirements Provides regulatory updates and guidance to investigators and research staff of new or changed regulations; participates in audits and site visits Minimum Education Required Bachelor's Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required. Qualifications 1 year experience in research or administrative capacity working on research projects; knowledge of research regulations, guidelines and compliance issues required; experience developing informed consent documents and preparing regulatory documents desired; experience and knowledge of IRB and federal or industry sponsor processes and requirements preferred. Additional Information: The OSUCCC - James is the only cancer program in the United States that features a National Cancer Institute (NCI)-designated comprehensive cancer center aligned with a nation-ally ranked academic medical center and a freestanding cancer hospital on the campus of one of the nation's largest public universities. Location: Remote Location 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. The Ohio State University

Job Tags

Remote job, Shift work, Day shift,

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