CRA II - Sponsor Dedicated

Fortrea; Warszawa; On-site; PLN 60,000 - 80,000; Full time

Benefits offered by this job

Clear career progression

Supportive and collaborative team environment

Job summary

A global biopharmaceutical company in Poland is seeking an experienced CRA II to manage site monitoring activities for one sponsor. In this role, you will perform various site monitoring responsibilities, ensuring patient safety and data quality. Candidates should have a degree in Life Sciences or Nursing and at least 2 years of experience in independent monitoring, fluent in English and Polish. The company offers clear career progression and a supportive team environment.

Qualifications

• Minimum 2 years of independent monitoring experience in Pharma/CRO.
• Experience in interventional studies required.
• Willingness to work in Oncology preferred.

Responsibilities

• Perform site monitoring activities including initiation and close‑out visits.
• Manage clinical sites per project plans and regulatory requirements.
• Prepare accurate monitoring and trip reports.

Skills

Independent monitoring experience

Knowledge of SAE reporting

Collaboration

Fluent in English

Fluent in Polish

Education

University degree in Life Sciences or Nursing

Job description

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

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