Poland CRA: Site Monitoring & Study Oversight

IQVIA; Warszawa; On-site; PLN 133,000 - 280,000; Full time

Job summary

IQVIA is seeking experienced CRAs for our Site Management Team in Poland. You will perform site monitoring visits across multiple protocols and sites, ensuring GCP/ICH compliance and timely data capture. Travel to sites will be required, and you will collaborate with study teams to support recruitment plans and trial milestones.

Fluency in Polish and English is essential. Join IQVIA to contribute to high-quality clinical research services and patient outcomes across a dynamic multi-sponsor

Qualifications

• Life sciences degree required.
• Independent on-site monitoring experience expected.
• Experience across multiple protocols/sites and drug indications.
• Willingness and ability to travel.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per contracted scope and GCP/ICH.
• Collaborate with sites to drive and track subject recruitment.
• Administer protocol training and maintain lines of communication with sites.
• Evaluate site practices for protocol conduct and regulatory adherence.
• Track regulatory submissions, recruitment, CRF completion and data queries.
• Maintain TMF/ISF documentation per regulatory requirements.
• Document site management activities and submit visit reports.

Skills

Strong communication

Polish language

English language

Education

Life science degree

Job description

IQVIA is seeking experienced CRAs for our Site Management Team in Poland. You will perform site monitoring visits across multiple protocols and sites, ensuring GCP/ICH compliance and timely data capture. Travel to sites will be required, and you will collaborate with study teams to support recruitment plans and trial milestones.

Fluency in Polish and English is essential. Join IQVIA to contribute to high-quality clinical research services and patient outcomes across a dynamic multi-sponsor