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
Associates Degree (± 13 years)
Experience/Background
Experience
Experience Details
Minimum 1 year
Licenses and Certifications
Language Proficiency
Language
Proficiency
