Pharmaceutical Quality GVP Auditor – Freelance/Independent Consultant
Advarra
part-time
Posted on:
Location Type: Hybrid
Location: Wawa • United States
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Job Level
About the role
- Conduct Good Pharmacovigilance Practice (GVP) audits (planning, agenda, physical or remote audit, and report writing)
- Evaluate investigator sites, CROs, and vendor compliance or qualification
- Prepare comprehensive audit reports detailing findings and root-causes
- Provide written audit reports in English
- If required will provide corrective actions support and present findings to QA leadership and stakeholders
- Work collaboratively with clients to ensure quality standards
Requirements
- Minimum 10+ years of Clinical Quality Assurance and/or Good Pharmacovigilance Practice (GVP) experience
- Minimum 5+ years of Good Clinical Practices auditing experience
- Demonstrated experience with regulatory agency expectations (e.g., FDA, EMA) and audit readiness activities
- Demonstrated experience in developing and implementing quality assurance plans, audit programs, and corrective action plans
- Fluent English communication, verbal and written
- Bachelor's degree
Benefits
- Part-Time
- Hybrid
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
Good Pharmacovigilance Practice (GVP)Clinical Quality AssuranceGood Clinical Practices auditingregulatory agency expectationsaudit readiness activitiesquality assurance plansaudit programscorrective action plansreport writingcompliance evaluation
Soft Skills
collaborationcommunicationpresentation skillsattention to detailanalytical thinkingproblem-solvingstakeholder engagementleadershiporganizational skillswritten communication