Principal Database Programmer

3 hours, 11 minutes ago
Full-time
Lead
Software Development
Precision Medicine Group

Precision Medicine Group

Precision Medicine Group specializes in precision medicine, utilizing targeted expertise and data insights to accelerate drug development and enhance the commercialization of next-generation medical products for the pharmaceutical and life sciences ind...

Pharmaceuticals
251-1K
Founded 2012

Description

  • Manage assigned projects, including delivery timelines, scope, budgets, forecasting, and resource requirements.
  • Design, build, maintain, test, and validate clinical databases, applications, and third-party integrations.
  • Provide database administration, advanced technical support, troubleshooting, and issue resolution.
  • Support data management activities from CRF design through database close and archival.
  • Develop and maintain study-specific validation documentation, SOPs, and process documentation.
  • Lead operational study and programming teams and provide training to end users, junior staff, and data management team members.
  • Collaborate with clients, sponsors, vendors, project managers, data management teams, and EDC providers to gather requirements and communicate status.
  • Conduct EDC demonstrations, software trainings, project presentations, and vendor selection activities.
  • Ensure activities comply with SOPs, regulatory requirements, government guidelines, and industry standards.
  • Support onboarding and cross-functional or organization-wide initiatives as needed.

Requirements

  • At least 8 years of relevant experience and a bachelor’s degree or equivalent related experience.
  • Strong clinical database programming and clinical database management system development experience.
  • Strong experience with Rave and Veeva, plus proficiency in more than one CDMS.
  • Experience building forms, edit checks, complex rules, and maintaining CRF standards libraries.
  • Experience with object-oriented programming languages such as C#, C++, or VBS.
  • Understanding of CDISC standards, including CDASH, SDTM, and ADaM.
  • Strong oncology experience; autoimmune disease experience preferred.
  • Experience in a clinical, scientific, or healthcare discipline and across multiple therapeutic areas preferred.
  • Proficiency with Microsoft Word, Excel, PowerPoint, and Outlook.
  • Strong leadership, communication, organization, prioritization, interpersonal, negotiation, and client relationship skills.
  • Ability to work independently, manage time, create project plans, and collaborate effectively with minimal direction.
  • Professional proficiency in written and spoken English; willingness to travel occasionally.

Benefits

  • Fully remote work from European locations.
  • Full-time, permanent employment.
  • Equal opportunity employer with reasonable accommodation support for applicants with disabilities.

Interested in this position?

Apply directly on the company website

Apply Now

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