Experienced Clinical Research Associate, Site Management Poland

Experteer Overview In this field-based role, you'll monitor clinical sites to ensure GCP/ICH conformance while supporting patient recruitment and study execution.
You'll work closely with sites to maintain high-quality data, manage regulatory submissions, and keep TMF/ISF documentation up to date.
You'll collaborate with cross-functional teams to drive study progress across multiple sites and protocols.
This is an opportunity to contribute to life-changing medicines and gain broad exposure to site activation and monitoring in a dynamic, sponsor-driven environment.
Compensaciones / Beneficios
• Perform site monitoring visits (initiation, monitoring, close-out) per scope and regulatory requirements
• Support site recruitment plans to align with project needs
• Provide protocol training to sites and maintain regular communication on study expectations
• Assess site practices for protocol adherence and regulatory compliance; escalate issues as needed
• Track regulatory submissions, approvals, recruitment, CRF completion, data queries; may support start-up
• Ensure TMF/ISF documentation is complete and compliant
• Document site management activities and visit findings through reports and letters
• Collaborate with study team members for project execution support
• May assist in developing site-specific recruitment plans
• May be accountable for site financial management per clinical trial agreement and invoicing requirements Responsabilidades
• life science degree educated
• experience in independent on-site monitoring
• handled multiple protocols/sites across various drug indications
• flexible with travel
• strong communication, written and presentation skills
• fluent in Polish and English Requisitos principales •