Clinical Quality / GCP Consultant
About the Company
ProPharma is seeking an experienced Clinical Quality / GCP professional to provide specialist support as part of a Clinical SWAT resource for a medical device sponsor. This is a 3-month contract commencing in October 2026, requiring approximately 20 hours per week. The assignment requires a standard GCP-level resource and can be delivered remotely across Europe.
About the Role
The key objective is to provide an expert assessment confirming that the global quality-system overlay is sufficient, appropriately implemented, and that the relevant sites are compliant with applicable GCP requirements.
Responsibilities
Support CAPA implementation and effectiveness follow-up activities.Review the implementation of the global Clinical Quality System across multiple site locations.Assess whether the quality-system overlay provides appropriate coverage and control at site level.Evaluate site processes and practices against applicable GCP requirements.Identify any gaps, inconsistencies, or potential compliance risks.Provide practical, risk-based recommendations where required.Assess the effectiveness and sustainability of implemented CAPAs.Support the documentation and follow-up of findings and actions.Work collaboratively with Clinical Operations and Quality stakeholders to support successful implementation.
Qualifications
We are looking for an experienced Clinical Quality / GCP professional who is comfortable working in a Clinical SWAT capacity, providing focused expert support to address a defined quality and compliance requirement.
Required Skills
The ideal resource will have a strong understanding of GCP, clinical quality, CAPA, quality systems and site compliance, with the ability to independently assess processes, identify gaps and provide practical recommendations.