Clinical Programmer
Covington, KY · On-site +1
A Clinical Programmer will support the design, development, and validation of clinical trial ... In this role, you will build and test study databases using platforms such as Medidata Rave or ...
Clinical Programmer
Covington, KY · On-site +1
A Clinical Programmer will support the design, development, and validation of clinical trial ... In this role, you will build and test study databases using platforms such as Medidata Rave or ...
Clinical Programmer
Covington, KY · On-site +1
A Clinical Programmer will support the design, development, and validation of clinical trial ... In this role, you will build and test study databases using platforms such as Medidata Rave or ...
Clinical Programmer
Covington, KY · On-site +1
A Clinical Programmer will support the design, development, and validation of clinical trial ... In this role, you will build and test study databases using platforms such as Medidata Rave or ...
Remote Medidata Rave Programmer information
What are the key skills and qualifications needed to thrive as a Remote Medidata Rave Programmer, and why are they important?
To thrive as a Remote Medidata Rave Programmer, you need a solid background in clinical data management, database programming, and a relevant scientific or technical degree. Expertise in Medidata Rave EDC systems, eCRF design, and familiarity with CDISC standards or certifications are typically required. Strong attention to detail, problem-solving ability, and effective remote communication skills set outstanding programmers apart. These competencies ensure accurate, compliant, and efficient clinical trial data capture, which is critical for successful drug development and regulatory submissions.
What are the main challenges faced by Remote Medidata Rave Programmers, and how can candidates prepare for them?
Remote Medidata Rave Programmers often encounter challenges such as navigating complex study build requirements, ensuring data integrity, and effectively collaborating with cross-functional teams in a virtual environment. Staying organized, maintaining clear communication, and regularly updating stakeholders are essential for success. Familiarity with Medidata Rave’s tools and participating in ongoing training can help you stay current with platform updates and industry standards.
What is a Remote Medidata Rave Programmer?
A Remote Medidata Rave Programmer is a specialized professional who works from a remote location to design, develop, and maintain electronic data capture (EDC) systems using the Medidata Rave platform. They create and configure study databases, build electronic case report forms (eCRFs), and ensure data integrity in clinical trials. Their work supports the collection, validation, and management of clinical trial data, helping pharmaceutical and biotech companies comply with regulatory requirements. These programmers often collaborate with data managers, clinical teams, and other stakeholders to deliver efficient and accurate solutions.
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Full-time
Medical, PTO
Posted 22 days ago
Job description
A Clinical Programmer will support the design, development, and validation of clinical trial databases. In this role, you will build and test study databases using platforms such as Medidata Rave or OmniComm TrialMaster, program validation checks, and ensure all data structures align with approved CRFs and study specifications. You will perform comprehensive user acceptance testing, support data cleaning through query management, and maintain complete documentation in accordance with SOPs. This position requires strong analytical skills, accuracy, and the ability to collaborate effectively with Clinical Data Managers and crossfunctional study teams to deliver highquality, auditready clinical data on time and within budget
What You'll Do:
- 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
What You'll Bring:
- 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
- Database experience with OmniComm TrialMaster or Medidata Rave is preferred
Why CTI?
- Advance Your Career – We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.
- Join an Award-Winning and Valued Team – We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.
- Make a Lasting Impact – We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.
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.com email 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
- We will never communicate directly with you via Microsoft Teams Messaging or by text message
- We will never ask for your bank account information at any point during the recruitment process
Equal Opportunity Employer/Veterans/Disabled