CRA II - Sponsor Dedicated

We are hiring an experienced CRA II to join our sponsor‑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 on Serious 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 in Life Sciences or Nursing
• Minimum 2 years of independent monitoring experience in Pharma/CRO
• Experience in interventional studies
• Strong knowledge of SAE reporting
• Oncology experience is a plus (or willingness to work in Oncology)
• Fluent English and Polish

Why join?

• Dedicated to one sponsor
• Exposure to complex, international studies
• Clear career progression
• Supportive and collaborative team environment

Learn more about our EEO & Accommodations request here .