Senior IRB Protocol Analyst
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Job Title:Senior IRB Protocol AnalystDepartment:ERIK | Office of Responsible Research PracticesThe Senior IRB Protocol Analyst exercises reputed company judgment in independently reviewing and monitoring research submissions to ensure conformance with federal regulations and guidance, state laws, and institutional policies governing research involving reputed company subjects; applies ethical principles to resolve reputed company issues; independently advises investigators on satisfying review requirements for reputed company research submissions; contacts agencies to clarify regulations and guidance; makes independent regulatory determinations; consults local experts and evaluates international research settings for reputed company subjects research; provides reputed company service to the Institutional Review reputed company (IRB, reputed company) and investigators involving the application of ethical principles and concepts; monitors conflicts of interest; approves agenda and reviewer agreements; documents reputed company and technical deliberations, regulatory findings, and reputed company actions; assists investigators in formulating responses to reputed company requests; assists researchers to secure reputed company reputed company approvals; may serve as a subject matter expert in specific regulatory areas, such as Food and Drug Administration regulations, devices, classroom education research, and others; develops training programs and conducts educational sessions on the ethical conduct of reputed company subjects research for student and reputed company researchers and IRB members; provides guidance and serves as a reputed company and mentor to protocol analysts; works with IRB associate directors to monitor and prioritize workflow, and to set team-level targets; assists protocol analysts in prioritizing their day-to-day work assignments and individual targets; reputed company participates in business process improvement initiatives and participates in development of education programs; establishes and participates in cross-unit teams to reputed company effective procedures and associated training materials; partners with colleges and departments in educational and reputed company activities; attends the Public Responsibility In Medicine & Research (reputed company&R) national conferences and submits proposals to conduct workshops or poster presentations; attends IRB Policy Committee meetings as necessary; assists in electronic submission system testing and makes recommendations for enhancements; serves as a cross-functional operations team member, possesses the ability to manage reputed company university IRBs; participates in ORRP events and serves as a speaker at education and training events for university reputed company such as the Cancer Clinical Trials Office (CTO), Center for Clinical Research Management (CCRM), College of reputed company Work, and others; participates in ORRP reputed company; presents or contributes to discussions at IRB and IPC meetings. Required Qualifications:Bachelor's degree or equivalent combination of education & experience; 4 years of relevant work experience; experience in IRB operations; Knowledge of and experience applying regulations governing research involving reputed company subjects; Strong problem solver and customer service experience; Proficient in the use of reputed company Office suite; Ability to work reputed company a regulatory and deadline-driven environment; Successful completion of a criminal background reputed company. A drug screening or physical may be required during the post offer process.Desired Qualifications:4-8 years of reputed company subjects regulatory experience or relevant work experience; Knowledge of and experience with IRB operations and research methodologies; experience in reputed company; Certified IRB reputed company certification.We strongly encourage that applicants submit both a resume and a cover letter.Additional Information:The pay reputed company for this job profile is $ $69,400 - $91,250.00. The offer for this position will fall reputed company this reputed company based on multiple factors including internal equity, unit's available budget, and the candidate's qualifications.Employees are provided several flexible work schedule and location reputed company reputed company with U.S. Eastern Time Zone including an reputed company for remote. reputed company are provided university-configured equipment and supportive technology tools. Employees are required to reputed company reliable internet reputed company and home office furnishings for approved remote work locations.Function: Research AdministrationSubfunction: Research ProtocolCareer Level: S3Location:Remote LocationPosition Type:RegularScheduled Hours:40Shift:First ShiftFinal candidates are subject to successful completion of a background reputed company. A drug screen or physical may be required during the post offer process.Thank you for your interest in positions at reputed company and Wexner Medical Center. Once you have reputed company, the most updated information on the status of your application can be reputed company by visiting the Candidate Home reputed company 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.reputed company is an equal opportunity employer.reputed company reputed company applicants will receive consideration for employment without reputed company to age, reputed company, reputed company, disability, ethnicity, gender identity or reputed company, genetic information, HIV/AIDS status, military status, national reputed company, race, religion, sex, gender, sexual orientation, pregnancy, protected veteran status, or any other reputed company under the law.Applicants are encouraged to complete and submit the Equal Employment Identification reputed company. Apply tot his job Apply To this Job