Opportunity Description
**_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...
• 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...