Clinical QC Compliance Associate III

Lake County, IL, US
Mar 30, 2019
Required Education
Bachelors Degree
Position Type
Full time
  • Responsible for compliance with applicable Corporate and Divisional policies and procedures.
  • Coordinates the activities of a cross-functional team to ensure completion of one or more projects are done on time, with quality and within budget (if applicable)
  • Lead project activities such as QC planning and implementation, metrics development and preliminary interpretation, compliance assessment and system updates, scientific publication compliance activities, QC planning to ensure demand is met, quality updates to standard documents and process enhancements.
  • Identify issues that potentially impact evaluable study data, ethical study conduct and ICH and AbbVie compliance and identify potential interventions or solutions to manage the issues .

Level will be based on education and years of experience.

  • Bachelor's degree (or equivalent ex-US) is required, typically in nursing or scientific field. An Associate's degree/R.N. (or equivalent ex-US) with relevant experience is acceptable.
  • Must have 4+ years of Pharma-related/ clinical research related experience.
  • Must have demonstrated a high level of core and technical competencies.
  • Possesses good communication skills.
  • Competent in application of standard business procedures (SOPs, ICH, Global Regulations, Ethics and Compliance).
  • Preferred exposure to clinical research from study initiation through study completion .