Das ist der Job
Auditors support compliance reviews across GCP clinical sites and vendors.
Darum lohnt es sich
Pharmaceutical Quality GCP Auditors (Consulting)
Job Category: Expert
Requisition Number: PHARM004113
• Posted: July 8, 2026
• Part-Time
• Remote
Locations
Remote - Germany
This role is open to candidates based in Germany.
Job Overview Summary
Advarra is seeking Good Clinical Practice (GCP) Auditors to join our consultant network for German-based projects.
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.
• If required will provide corrective actions support and present findings to QA leadership and stakeholders
• Work collaboratively with clients to ensure quality standards.
Basic 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
• B2 level in German communication, verbal and written
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.
