Sezzle is seeking a Principal Database Programmer to help build the foundation of clinical data operations in LATAM. You will lead the development, testing, implementation, and support of clinical databases from start-up through post-lock, partnering closely with Data Management, Project Management, EDC vendors, and clients.
What You'll Do
- Maintain responsibility for assigned projects, ensuring on-time delivery and communicating status to internal teams.
- Manage project forecasting of hours, resource requirements, and budgets, including identification of out-of-scope work.
- Provide input and guidance on the design of clinical databases to clients and internal teams.
- Build, support, and troubleshoot clinical databases and associated software.
- Develop, test, and validate programs and clinical databases for client projects and third-party applications.
- Provide system administration and advanced technical support for internally developed applications and databases.
- Develop and maintain study-specific validation documents.
- Support data management from CRF design through post-database close and archival.
- Participate in software vendor selection, EDC demonstrations, and trainings.
- Contribute to the development and maintenance of Standard Operating Procedures (SOPs) and process documentation.
- Support onboarding of new hires and provide leadership for cross-functional initiatives.
- Train data management project team members and communicate with study sponsors and vendors as needed.
- Present software demonstrations, training sessions, and project meetings.
What We're Looking For
- Minimum of 8 years’ relevant experience.
- Bachelor's degree and/or a combination of related experience.
- Professional working proficiency in English required.
- Proficiency in Microsoft Office: Word, Excel, PowerPoint, Outlook.
- Experience in Object Oriented Programming (C#, C++, VBS, etc.).
- Understanding of CDISC standards (CDASH, SDTM, ADaM, etc.).
- Experience in clinical database management system development.
- Experience in a clinical, scientific, or healthcare discipline.
- Proficiency in more than one CDMS system, including building forms, edit checks, and complex rule development.
- Awareness of CRF standards and input to maintenance of standards library.
- Ability to troubleshoot technical issues and build solutions.
- Broad knowledge of drug, device and/or biologic development and effective data management practices.
- Strong leadership, interpersonal, organizational, and communication skills.
- Able to handle a variety of clinical research tasks.
Nice to Have
- Experience in a clinical, scientific or healthcare discipline with multiple therapeutic area experience, preferably Oncology.
- Experience in utilizing various Database Programming systems.
Technical Stack
- Microsoft Office
- Object Oriented Programming (C#, C++, VBS)
- CDMS systems
Team & Environment
You will partner with Data Management, Project Management, EDC vendors, and clients.
Work Mode
This is a remote position open to candidates located in Argentina, Brazil, Chile, Colombia, Mexico, or Peru.
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
