Clinical Trial Designer

Job Summary

Creating high-quality data collection tools for new clinical trials, the full-time EDC Clinical Trial Designer will facilitate the design, development, documentation, testing, and implementation of clinical eCRF databases while ensuring compliance with standard operating procedures and trial-specific guidelines.

Key responsibilities

• Design eCRF forms using Oracle InForm/Central Designer or Veeva CDMS/Studio based on detailed data collection requirements
• Produce annotated study books and validate study design for forms and schedules
• Conduct meetings with study teams to communicate project timelines and requirements while applying lessons learned from previous studies

Required qualifications

• BA/BS degree or equivalent experience
• Minimum of 2 years of Clinical Data Management experience using electronic data capture systems
• Familiarity with clinical research processes and CDISC/CDASH/SDTM standards is preferred
• Experience in the planning and management of clinical trials in the biopharmaceutical industry is preferred
• Strong commitment to high-quality work and customer service