[Hiring] Pharmaceutical Quality GCP Auditors Freelance/Independent (Consulting) @Advarra

Role Description

Advarra is seeking Good Clinical Practice (GCP) Auditors to join our consultant network for United Kingdom-based projects. Auditors support compliance reviews across GCP clinical sites and vendors.

Job Duties & Responsibilities

• Conduct Good Clinical Practice (GCP) 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, provide corrective actions support and present findings to QA leadership and stakeholders.
• Work collaboratively with clients to ensure quality standards.

Qualifications

• Minimum 10+ years of Clinical Quality Assurance and/or Good Clinical Practice (GCP) 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.
• B2 level in English communication, verbal and written.
• Bachelor's degree.

Preferred Qualifications

• Strong interpersonal and client interaction skills.
• Excellent analytical, problem-solving, communication, and report-writing skills.
• Ability to work collaboratively across departments and interact with internal and external stakeholders.