Clinical Research Associate

Location: Poland, ideally central Poland; fully remote option available

Minimum annualized starting base pay: 113,000 PLN per year

Company

hirify.global supports biotech, medtech, and specialty pharma companies in developing medicines, medical devices, and diagnostics.

What you will do

• Prepare timely, high-quality monitoring reports for sponsor approval according to Clinical Monitoring Plan timelines.
• Conduct remote and onsite monitoring focused on data integrity, patient safety, and applicable country regulations.
• Plan daily monitoring activities, set site priorities, and conduct qualification, initiation, interim monitoring, and close-out visits.
• Maintain the Trial Master File and electronic Trial Master File according to organizational filing processes.
• Review site documents for accuracy, completeness, currency, and required updates.
• Submit travel and monitoring expenses in line with company requirements.

Requirements

• Degree or international equivalent in a clinical, scientific, or health-related field, a registered healthcare qualification, or equivalent work experience.
• At least one year of independent clinical monitoring experience.
• Experience supporting Phase II and Phase III clinical studies.
• Experience in neurology, oncology, dermatology, or other relevant therapy areas.
• Ability to work remotely from Poland; applications are ideally based in central Poland.
• Knowledge of essential clinical-trial documents and ICH/GCP Section 8 requirements.

Culture & Benefits

• Flexible working arrangements designed to support work-life balance.
• Opportunities to develop skills and advance professionally.
• Health insurance, life insurance, retirement plan, paid time off, and an Employee Assistance Program may be included.
• Compensation is intended to be fair and competitive with market standards.