**MAIN PURPOSE OF ROLE** • Individual contributor representing the most common entry point for this career stream. • Works under direct supervision. **MAIN RESPONSIBILITIES** • Primary responsibility is ensuring implementation of quality plan at every stage of the Clinical Trial process/operations. • Implement quality assurance regulations. • Write and revise standard operating procedures. • Support and facilitate audits and regulatory inspections. • Support Quality Assurance Manager in supervision of all quality control aspects of the process (laboratories studies, clinical research, testing, operations). • Ensure that standards are met and report potential issues either with quality or reliability of testing procedures. • Lead implementation of new regulations. • May support quality training. **QUALIFICATIONS** High School Diploma / GED An Equal Opportunity Employer Abbot welcomes and encourages diversity in our workforce. We provide reasonable accommodation to qualified individuals with disabilities. To request accommodation, please call 224-667-4913 or email corpjat@abbott.com