Clinical Compliance Operations Specialist

📋 Description

• Facilitate and manage GCP project audits
• Ensure adherence to Veeva processes
• Promote GCP compliance across products and services
• Author GxP records and project audit reports
• Review project deliverables and manage incidents
• Collaborate with cross-functional teams globally

🎯 Requirements

• Bachelor’s degree or equivalent experience
• 3+ years in Clinical QA in Life Sciences
• Experience with Quality Management Systems
• Knowledge of ISO 9001 or GCP/QA guidelines
• Strong technical writing skills
• Excellent communication and time management

🎁 Benefits

• Remote work with UK/EU flexibility
• Work Anywhere culture