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Database Programmer

Alimentiv

Toronto, ON; Montreal, QC; San Diego, CA; Chicago, IL; Boston, MA; Newark, NJ; Raleigh-Durham, NC; Philadelphia, PARemotePosted 4 days ago$75,000 - $125,000/year
Full TimeEntry LevelBioinformatics & Data ScienceCRO
Original posting ↗

Summary

The Database Programmer is responsible for the design, development, testing, maintenance, and archiving of clinical study databases throughout the study lifecycle. This role will play a key part in supporting the deployment, adoption, and ongoing development of Medidata Rave EDC as Alimentiv expands its Electronic Data Capture (EDC) capabilities. The successful candidate will bring hands-on experience with Medidata Rave EDC and C# programming to develop custom functions, support database configurations, and contribute to clinical database programming activities independently. Working closely with internal project teams and sponsors, this position will help ensure successful database delivery, technical support, and continuous improvement.

Job description

Job Overview

The Database Programmer is responsible for the design, development, testing, maintenance, and archiving of clinical study databases throughout the study lifecycle. This role will play a key part in supporting the deployment, adoption, and ongoing development of Medidata Rave EDC as Alimentiv expands its Electronic Data Capture (EDC) capabilities. The successful candidate will bring hands-on experience with Medidata Rave EDC and C# programming to develop custom functions, support database configurations, and contribute to clinical database programming activities independently. Working closely with internal project teams and sponsors, this position will help ensure successful database delivery, technical support, and continuous improvement.

Key Responsibilities

  • Design, build, test, and maintain clinical study databases throughout the study lifecycle.
  • Support the deployment, implementation, and ongoing adoption of Medidata Rave EDC across clinical studies.
  • Develop, program, and test custom functions using C# to support Medidata Rave EDC functionality.
  • Create annotated electronic Case Report Forms (eCRFs) and program automated edit checks to support data validation.
  • Develop and test files required for electronic data uploads, data transfers, and integrations.
  • Program and generate clinical data listings and project tracking reports to support ongoing studies.
  • Manage database access, process change request (CR) publishing requests, and archive electronic data and documentation upon study completion.
  • Troubleshoot and resolve database programming issues, providing technical expertise and support to internal teams and sponsors.
  • Communicate database setup progress, project milestones, and technical issues to internal and external stakeholders.
  • Contribute to the development and improvement of database programming processes and departmental procedures.

Skills & Qualifications

  • A post-secondary certificate or diploma from a college, training institute, or equivalent institution. An equivalent combination of education and experience may be considered.
  • A minimum of 1–3 years of related database programming experience, with 4–6 years preferred.
  • Hands-on experience with Medidata Rave EDC, including clinical database development, configuration, and maintenance.
  • Proficiency in C# programming, with the ability to independently develop, test, and troubleshoot custom functions within Medidata Rave EDC.
  • Experience developing and maintaining electronic Case Report Forms (eCRFs) and automated edit checks.
  • Knowledge of clinical database programming processes, including data transfers, electronic data uploads, and reporting.
  • Experience generating clinical data listings and project tracking reports.
  • Strong technical troubleshooting and problem-solving skills, with the ability to independently address database programming challenges.
  • Effective communication and collaboration skills, with the ability to work with internal project teams, sponsors, and external stakeholders.
  • Strong organizational skills, attention to detail, and the ability to manage competing priorities and meet project milestones.

Requirements

  • Post-secondary certificate or diploma from a college, training institute, or equivalent institution
  • Minimum of 1–3 years of related database programming experience
  • Hands-on experience with Medidata Rave EDC, including clinical database development, configuration, and maintenance
  • Proficiency in C# programming, with the ability to independently develop, test, and troubleshoot custom functions within Medidata Rave EDC
  • Experience developing and maintaining electronic Case Report Forms (eCRFs) and automated edit checks
  • Knowledge of clinical database programming processes, including data transfers, electronic data uploads, and reporting
  • Experience generating clinical data listings and project tracking reports
  • Strong technical troubleshooting and problem-solving skills
  • Effective communication and collaboration skills
  • Strong organizational skills, attention to detail, and ability to manage competing priorities

Benefits

  • Education Reimbursement
  • Cell Phone Allowance
  • Remote Work Allowance
  • Office Setup Allowance
  • Working While Visiting Program
  • Flexible Summer Hours
  • Employee Referral Incentive
  • Alimentiv Trust
  • Mentorship Program
  • Short-Term Incentive Plan

Company overview

Alimentiv is a leading specialty gastrointestinal (GI) contract research organization (CRO) founded in 1986 and headquartered in London, Ontario, Canada. The company operates as a full-service CRO specializing in GI clinical trials, with deep expertise in inflammatory bowel disease (IBD), eosinophilic gastrointestinal diseases (EGIDs), celiac disease, and other GI disorders. Alimentiv provides comprehensive clinical research services including clinical trial management, medical monitoring, medical imaging solutions, precision medicine/biomarker services, histopathology, biostatistics, and real-world evidence generation. The company supports over 70% of all IBD compounds currently in development and maintains a global network of 5,000+ clinical trial sites across more than 60 countries. With approximately 501-1,000 employees and offices in Canada, the United States, Europe, and Australia, Alimentiv combines academic excellence with operational expertise to accelerate drug development timelines and improve clinical trial outcomes for pharmaceutical and biotechnology partners.

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