MAIN PURPOSE OF THE 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
Education
Education Level Major/Field of Study or Equivalent
High School Diploma / GED
Experience/Background
Experience Experience Details
No Experience
The base pay for this position is
N/AIn specific locations, the pay range may vary from the range posted.