Regulatory Compliance Officer - CCC | Clinical Trials Office at InsideHigherEd

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Job Title:Regulatory Compliance Officer - CCC | Clinical Trials OfficeDepartment:CCC | Clinical Trials OfficePosition SummaryThe 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.ResponsibilitiesCollaborates with investigators during study development to facilitate and confirm that appropriate regulatory safeguards have been includedConducts detailed reviews of assigned protocols and informed consent forms prior to IRB reviewEnsures timely submission of protocol documents for review by appropriate agency communicates with all CTO research projects sponsors (academic, federal, industry) to ensure complianceInterfaces with various internal and external entities to coordinate and effectively compile all appropriate data relevant to the conduct of a CTO trialDevelops IRB submission packets for protocols, including writing of abstract, submission of standard forms and drafting of informed consent formsProvides and maintains tracking system to assess progress of a protocol's review; maintains regulatory essential files on submitted and approved studiesReviews all protocol revisions and amendments; amends consent forms if needed and follows established guidelines to determine if amendments requires IRB reviewDistributes all amendments and IRB approved informed consent forms to relevant university protocol holdersActs 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 timelyAttends meetings; serves as principal contact from CTO to regulatory agencies including FDA and IRBsContinually monitors federal and sponsor rules, regulations and processes to identify and interpret new, updated or changed requirementsProvides regulatory updates and guidance to investigators and research staff of new or changed regulations; participates in audits and site visitsJob RequirementsBachelor’s Degree in biological sciences, health sciences, social sciences or other medical field or an equivalent combination of education and experience required; one 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:As one of only 50 designated comprehensive cancer centers in the nation, The Ohio State University Comprehensive Cancer Center – Arthur G. James Cancer Hospital and Richard J. Solove Research Institute is dedicated to the creation of knowledge in laboratory, clinical and population-based cancer research. We apply those discoveries to develop more effective approaches to cancer prevention, diagnosis, and therapies – providing tomorrow’s standard of care today. A Cancer-Free World Begins Here. Location:Remote LocationPosition Type:RegularScheduled Hours:40Shift:First ShiftFinal 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. As required by Ohio Revised Code section 3345.0216, Ohio State will: educate students by means of free, open and rigorous intellectual inquiry to seek the truth; equip students with the opportunity to develop intellectual skills to reach their own, informed conclusions; not require, favor, disfavor or prohibit speech or lawful assembly; create a community dedicated to an ethic of civil and free inquiry, which respects the autonomy of each member, supports individual capacities for growth and tolerates differences in opinion; treat all faculty, staff and students as individuals, hold them to equal standards and provide equality of opportunity with regard to race, ethnicity, religion, sex, sexual orientation, gender identity or gender expression.