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Senior Consultant - Clinical Data Programming

🕒 3 days ago
EDC Clinical SoftwareData ManagementClinical Trial ProcessesSAS

📜 Description

  • Act as a trusted advisor to customers and clinical sites, ensuring trial designs are configured to meet their goals, and providing training and mentorship.
  • Work with customers to interpret clinical protocol requirements and project specifications, applying industry and Veeva best practices.
  • Lead database development activities per the project plan, coordinating with sponsors, CROs, and other vendor teams.
  • Coordinate with clinical data providers to configure data transfers.
  • Configure forms, rules, and other study items in Vault CDMS, and build custom SQL-based listings for data cleaning needs.
  • Run user acceptance testing, managing feedback and issue resolution.

🛠️ Requirements

  • 5+ years of experience with EDC clinical software, covering end-to-end data management.
  • Solid understanding of clinical trial processes, particularly around data collection and review.
  • Programming experience in languages such as SAS, R, JSON, Python, or SQL.
  • Background in the life sciences industry with experience in project assessment, planning, development, training, and implementation.
  • Experience in a customer-facing role within software professional services or consulting.
  • Strong verbal and written communication, interpersonal, and presentation skills.

Benefits

  • Private health insurance
  • Flexible paid time off plus local public holidays
  • Pension / retirement plan contributions

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