
CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com
What You'll Do
· Host Sponsor audits of CTI and assure that issues from Sponsor audits are promptly communicated to the appropriate team members, assist with the development of a corrective action plan and facilitate resolution of all audit findings
· Host Regulatory Authority inspections of CTI. Assist the organization in preparation for, coordination, hosting, conduct, documentation and follow-up of regulatory inspections
· Clearly communicate and report (verbally and in writing) audit outcomes and escalating significant compliance concerns to project teams, QA and CTI management and sponsor contacts appropriately
· Prepare training materials and conducting training related to relevant QA topics for CTI staff
· Report, manage and follow deviations, complaints, issues, non-conformances and their related CAPAs
· Prepare audit plans for audits and projects and programs, as needed
· Conduct Vendor Audits, Internal System Audits, Site Audits and Computerized Systems and Database Validation Audits. Identify and follow-up on any unresolved audit findings identified in a Quality Assurance Audit
· Conduct Sponsor-contracted audits, such as: Clinical Study Report Audits, Clinical Protocol Audits, Clinical Database Audits, Investigator Site Audits, etc. on an ad hoc or scheduled basis as determined by the Sponsor and CTI management
· Assist with creation, review, revision and management of SOPs
· Provide content and/or present quality related information at capabilities presentations
· Assist with completion of RFIs related to Quality Management Systems
· Assist in the review of Quality Assurance agreements related to projects or client master service agreements
· International region-specific functions
What You'll Bring
Why CTI?
Important Note
In light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.comemail address to guide you through our interview process. Please ensure you are applying for jobs directly on our website ( www.ctifacts.com) or from our verified LinkedIn page.
Please Note

CTI Clinical Trial and Consulting Services is a global, privately held, research service organization, delivering a complete spectrum of clinical trial and consulting services throughout the lifecycle of development, from concept to commercialization. CTI’s focused therapeutic approach provides pharmaceutical, biotechnology, and medical device firms with clinical and disease area expertise in rare diseases, regenerative medicine / gene therapy, immunology, transplantation, nephrology, hematology / oncology, neurology, infectious diseases, hepatology, cardiopulmonary, and pediatric populations. CTI also offers a fully integrated multi-specialty clinical research site and complete global laboratory services. Now in its third decade, CTI is one of the 20 largest contract research organizations in the world, with associates in more than 60 countries across six continents. CTI is headquartered in the Greater Cincinnati area, with operations across North America, Europe, Latin America, MEA, and Asia-Pacific. For more information, visit www.ctifacts.com.