Clinical Database Programmer @ Antal

Polsko

Required Qualifications:


  • Medidata Rave EDC Certified Study Builder
    • OR an equivalent combination of:
      • Medidata Rave Study Design and Build Essentials – Data Managers
      • Medidata Rave Study Design and Build Essentials – Data Validations


  • Hands-on experience building and validating Rave EDC systems in clinical trial settings.
  • Familiarity with GCP, GDP, and regulatory compliance processes.
  • Strong understanding of clinical data flow, SDTM mapping, and EDC best practices.
  • Excellent communication skills and ability to work collaboratively in cross-functional teams.
  • Experience working with SOPs and within a regulated environment.

? Nice to Have:


  • Experience with integration to enterprise data warehouses.
  • Prior exposure to medical device studies (e.g., Boston Scientific).
  • Experience with Rave Migration and Version Management tools.

Medidata Rave EDC Study Builder / Clinical Data Programmer


? Location: Poland / Remote
Employment Type: Full-time
? Contract Type:  B2B
? Industry: Clinical Research / Pharma / CRO

? Role Overview:


We are seeking a skilled Medidata Rave EDC Study Builder / Clinical Data Programmer to join our clinical data team. In this role, you will be responsible for developing and maintaining clinical trial databases using Medidata Rave EDC, ensuring compliance with Good Clinical Practice (GCP) and Good Documentation Practice (GDP). You will collaborate closely with Data Managers, Study Teams, Vendors, and Site Staff throughout the clinical study lifecycle.

,[Develop, test, validate, and maintain Medidata Rave EDC clinical trial databases., Create EDC design specifications: data dictionary, event definitions, eConsent, edit checks, branching logic, advanced query rules, calculated fields, dynamic forms, and event rules., Collaborate with Data Managers and Study Teams to design and build the database using global eCRF libraries., Configure and optimize user interfaces for various data collection methods (eCOA, EDC)., Develop test scripts and coordinate User Acceptance Testing (UAT) of the EDC system., Coordinate database go-live activities and manage production deployments., Perform batch data imports and support secondary data source transfers (e.g., lab or site data)., Support internal and external audits and inspections as a subject matter expert., Ensure adherence to company SOPs, guidelines, and regulatory standards (GCP/GDP)., Contribute to the development of EDC design standards to improve quality and efficiency.] Requirements: Rave EDC, GCP, GDP, Data warehouses

Kategorie

data

  • Podrobné informace o nabídce práce
    Firma: Antal
    Lokalita: Práce v Polsku
    Odvětví práce: data
    Pracovní pozice: Clinical Database Programmer @ Antal
    Směnnost práce fulltime - 40 hours per week
    Nástup do práce od: IHNED
    Nabízená mzda: neuvedeno
    Nabídka přidána: 7. 8. 2025
    Pracovní pozice aktivní
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Práce Clinical Database Programmer @ Antal: Často kladené otázky

👉 V jakém městě se nabízí nabídka práce Clinical Database Programmer @ Antal?

Práce je nabízena v lokalitě Remote, Warszawa.

👉 Jaká firma nabírá na tuto pozici?

Tato nabídka práce je do firmy Antal.

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