Sr. CRA – Site Management (Poland)

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

Benefits offered by this job

Health and welfare benefits

Job summary

IQVIA is seeking experienced CRAs for our Site Management Team in Poland. You will perform site monitoring visits across contracted scope in accordance with GCP and ICH guidelines, ensuring quality and regulatory compliance, and manage site communications.

Responsibilities include tracking recruitment, training sites, escalating issues, maintaining TMF/ISF documentation, and collaborating with the study team to support start-up activities and overall project execution.

Qualifications

• Life science degree required.
• Experience in independent on-site monitoring.
• Experience with multiple protocols/sites across drug indications.
• Flexibility to travel.
• Strong communication, written and presentation skills.
• Fluent in Polish and English.

Responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close-out) per contracted scope and GCP/ICH guidelines.
• Drive and track subject recruitment plans to enhance predictability.
• Administer protocol training and establish regular site communication to manage expectations.
• Evaluate site practices for protocol conduct and regulatory compliance.
• Escalate quality issues as appropriate.
• Track regulatory submissions, recruitment, CRF completion and data queries.
• Maintain TMF/ISF documentation and generate visit reports.
• Collaborate with study team for project execution and start-up support.

Skills

On-site monitoring

Communication skills

Travel flexibility

Multitasking

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 contracted scope in accordance with GCP and ICH guidelines, ensuring quality and regulatory compliance, and manage site communications.

Responsibilities include tracking recruitment, training sites, escalating issues, maintaining TMF/ISF documentation, and collaborating with the study team to support start-up activities and overall project execution.