job title: CDC 2 (Icon)

7/9/20251 min read

What you will be doing 

  • Assist Data Management Study Lead in maintenance of eCRF, Data Validation Specifications, and Study Specific Procedures.

  • Manage clinical and third-party data reconciliation based on edit specifications and data review plans.

  • Tracks and communicates status of study and task metrics to clinical data scientist, project team, and functional management.

  • Address data related questions and recommend potential solutions.

  • Identify root cause to systematically resolve data issues.

Your profile 

  • Bachelor's degree in a relevant field, such as Life Sciences or Healthcare.

  • Intermediate kNwledge of clinical data management within the pharmaceutical or biotechNlogy industry.

  • Familiarity with data management software and systems (e.g., Medidata, Oracle RDC, or similar).

  • Strong attention to detail and the ability to work effectively in a fast-paced environment.

  • Excellent communication skills and the ability to collaborate with cross-functional teams.

  • Knowledge of regulatory guidelines and standards (e.g., ICH-GCP) is a plus