Clinical Site Activation Specialist

Experis to światowy lider rekrutacji specjalistów i kadry zarządzającej w kluczowych obszarach IT.

• Bachelor’s degree in life sciences or a related field
• Minimum 3 years of clinical research experience, including 1 year in a coordination or leadership role
• Strong knowledge of GCP/ICH guidelines and local regulatory requirements
• Excellent communication, negotiation, and organizational skills
• Ability to manage multiple projects and work independently
• Experience with clinical trial systems and document management
• Fluency in English

• Serve as the Single Point of Contact (SPOC) for assigned studies at the site level
• Prepare, review, and track regulatory and contractual documents
• Ensure timely site activation in line with project timelines and quality standards
• Maintain internal systems and databases with accurate project-specific information
• Collaborate with Site Activation Managers, Project Managers, and other departments
• Provide local regulatory expertise and support during planning and execution
• Perform quality control of site documents and ensure compliance with GCP/ICH guidelines
• Monitor site performance metrics and contribute to continuous improvement initiatives