CTI Clinical Trial and Consulting Services · 8 hours ago
Clinical Programmer
Covington, KY
Full-time
Hybrid
Entry Level
1+ years expCTI Clinical Trial and Consulting Services is a company focused on advancing medicine by supporting clinical trials. The Clinical Programmer role involves designing, developing, and validating clinical trial databases, ensuring data accuracy, and collaborating with cross-functional teams to deliver high-quality clinical data.
BiotechnologyConsultingPharmaceutical
Responsibilities
Act as a primary database architect for client clinical databases using Medidata Rave, OmniComm TrialMaster, or other database applications as needed for Clinical Trials
Create database entry screens based on approved case report form (CRF) casebook
Perform internal testing of entry screens prior to user acceptance testing
Work with lead CP or Study Clinical Data Manager to implement system edits on built entry screens
Program validation procedures, in conjunction with the Sr. CP or CP II, for clinical studies and other billable projects. Validation procedures are programming code that output edit failures in CTI systems when checking the data against expected values. These expected values could be acceptable ranges or form flow edits/visit progression
Maintain necessary study build documentation as required by CTI SOPs
Meet all project deadlines on time and on budget
Ensure accuracy of clinical databases as compared to the CRF; perform user acceptance testing (UAT) of database and provide feedback to study team regarding any discrepancies
Perform UAT on programmed edits in the clinical database; ensure accuracy of edits in database as compared to edit specifications documents; provide feedback to study team on functioning of edits. The UAT the CP I performs is comprehensive and in conjunction with the Sr. CP or CP II direction. The programmers are to test the forms they have built as well as any edits or derivations that they have programmed
Perform review and issue queries for CRF data, based on automated edit checks, manual review, post-hoc data listings, and sponsor requirements
Maintain all necessary data review documentation to support accurate data cleaning
Qualification
Required
Bachelor's degree or equivalent experience in Computer Science/Information Technology or a technical degree in a related field
1+ years of experience working with databases in a complex clinical data management (CDM) environment, and/or equivalent combination of education and experience
Preferred
Database experience with OmniComm TrialMaster or Medidata Rave
Benefits
Career progression through a structured mentoring program
Leadership courses
Tuition reimbursement
Dedicated training department
Generous health benefits
Vacation packages
Hybrid work from home opportunities
Paid parental leave
CTI Cares program
Company
CTI Clinical Trial and Consulting Services
CTI is a full-service contract research organization (CRO), delivering a complete spectrum of clinical trial and consulting services.
1001-5000 employees
H1B Sponsorship
CTI Clinical Trial and Consulting Services has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2023 (1)
2020 (1)
Funding
Current Stage
Late StageLeadership Team
Timothy Schroeder
Chairman & CEO | Founder
Recent News
Medidata Solutions, Inc.
2025-11-04
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