The Clinical Process Compliance Associate is an independent contributor who assists the Quality Control, Compliance, and/or Metrics team with the oversight of clinical trial activities based on the standards required to ensure adherence to GCP and AbbVie procedures. They are aware of both internal and external business environment requirements and escalate issues to management and develops scenarios for issue resolution.

Responsibilities:

• Responsible for compliance with applicable Corporate and Divisional policies and procedures.
• Assists in the completion of activities regarding quality control, compliance, investigational product release for clinical studies and/or data collection; including working with functional areas to ensure assigned activities are completed per plan.
• Communicates clinical-related information and escalates issues to management with possible resolutions
• Maintains the SharePoint site and other systems required to support functional activities.