CDC II

Role & responsibilities

• 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.

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