CRA II - Sponsor Dedicated

We are hiring an experiencedCRA II to join oursponsor‑dedicated team in Poland. In this role, you’ll work exclusively with one sponsor, gaining deep study knowledge and long‑term project ownership, with strong opportunities for career growth.
 

Key Responsibilities

• Perform site monitoring activities (initiation, routine monitoring, and close‑out visits)
• Manage clinical sites in line with project plans, SOPs, and regulatory requirements
• Ensure patient safety, data quality, and audit readiness
• Review CRFs, perform source data verification, and resolve queries
• Track and follow up onSerious Adverse Events (SAEs)
• Prepare accurate monitoring and trip reports
• Support feasibility, QC visits, investigator recruitment, and regulatory submissions
• Collaborate with sponsors, investigators, and internal teams
• Support training and mentoring of new team members
   

Requirements

• University degree inLife Sciences orNursing
• Minimum 2 years of independent monitoring experience in Pharma/CRO
• Experience ininterventional studies
• Strong knowledge ofSAE reporting
• Oncology experience is a plus (or willingness to work in Oncology)
• Fluent English and Polish
   

Why join?

• Dedicated toone sponsor
• Exposure to complex, international studies
• Clearcareer progression
• Supportive and collaborative team environment

Learn more about ourEEO & Accommodations request here.