Remote Regional CRA II - Monitor & Ensure Data Integrity

Warman O'Brien; Polska; Hybrid; PLN 67,000 - 100,000; Full time

Benefits offered by this job

Company car or car allowance

Structured onboarding programme

Ongoing support and development

Job summary

Warman O'Brien is seeking a Clinical Research Associate II to join a growing clinical research team within a global biopharmaceutical company (FSP model). This remote regional role in Poland offers 70% of sites within 250 km of your home and ~8-10 monitoring days per month, with potential to manage up to five protocols.

As CRA, you will monitor trials, ensure protocol compliance, patient safety and data integrity per ICH-GCP standards, performing site qualification, initiation, routine

Qualifications

• BA/BS/BSc in Life Sciences, Healthcare or a related field.
• At least 1 year of independent monitoring experience preferred for CRA I/II.
• Fluent Polish and advanced English.
• Valid driving licence and willingness to travel.

Responsibilities

• Monitor clinical trials and ensure protocol compliance.
• Perform site qualification, initiation, routine monitoring and close-out visits.
• Review source data and resolve queries to ensure data integrity.
• Collaborate with investigators and site teams to support study delivery.

Skills

Organisation

Communication

Problem solving

Remote collaboration

Education

Bachelor's degree in Life Sciences/Healthcare

Job description

Warman O'Brien is seeking a Clinical Research Associate II to join a growing clinical research team within a global biopharmaceutical company (FSP model). This remote regional role in Poland offers 70% of sites within 250 km of your home and ~8-10 monitoring days per month, with potential to manage up to five protocols.

As CRA, you will monitor trials, ensure protocol compliance, patient safety and data integrity per ICH-GCP standards, performing site qualification, initiation, routine