CRA II - Sponsor Dedicated

Fortrea; United States; Remote; USD 39,000 - 55,000; Full time

Job summary

Fortrea is 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 include monitoring site visits (initiation, routine, close‑out), managing clinical sites, ensuring patient safety and data quality, reviewing CRFs, and SAE reporting.

Qualifications

• Independent monitoring experience in Pharma/CRO (minimum 2 years)
• Oncology experience is a plus
• Fluent English and Polish required

Responsibilities

• Perform site monitoring visits (initiation, routine monitoring, close-out)
• Manage clinical sites per project plans, SOPs and regulatory requirements
• Ensure patient safety, data quality and audit readiness
• Review CRFs, perform source data verification, resolve queries
• Track and follow up on SAEs
• Prepare 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

Skills

Monitoring experience

English proficiency

Site management

Education

Life Sciences degree

Nursing degree

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

Learn more about our EEO & Accommodations request here.