Clinical Research Associate – Remote Trials

Premier Research; Poland; Remote; PLN 102,000 - 124,000; Full time

Benefits offered by this job

Health insurance

Life insurance

Retirement plan

Paid time off

Employee Assistance Program

Job summary

Premier Research is seeking a Clinical Research Associate to join our Clinical Monitoring, Site Management and SSU team. This role helps transform ideas into medicines, ensuring patient safety and high-quality data across studies.

You will plan site visits, support Phase II and III trials, and collaborate with cross-functional teams to ensure regulatory compliance. Fully or partly remote options available for applicants in Poland.

Qualifications

• Undergraduate degree or international equivalent in clinical, science, or health-related field.
• Licensed health-care professional (e.g., registered nurse) or equivalent work experience.
• 1 year of independent monitoring experience in clinical research.
• Experience across therapy areas: Neurology, Oncology, Dermatology.
• Experience supporting Phase II & III studies.

Responsibilities

• Delivers quality, timely monitoring reports per the Clinical Monitoring Plan timelines.
• Maintains submission of expenses per travel and expense requirements.
• Monitors remotely, onsite, or other approved mode with focus on data integrity and patient safety per country regulations.
• Plans day-to-day monitoring activities and sets site priorities.
• Prepares for and conducts on-site visits (qualification, initiation, interim monitoring, close-out).
• Maintains TMF/eTMF per filing guidelines and understands essential documents per ICH/GCP Section 8.
• Reviews site documents for accuracy and updates.

Skills

Clinical monitoring

Data integrity

Regulatory compliance

Cross-functional collaboration

Education

Undergraduate degree in clinical/science/health

Tools

eTMF

Job description

Premier Research is seeking a Clinical Research Associate to join our Clinical Monitoring, Site Management and SSU team. This role helps transform ideas into medicines, ensuring patient safety and high-quality data across studies.

You will plan site visits, support Phase II and III trials, and collaborate with cross-functional teams to ensure regulatory compliance. Fully or partly remote options available for applicants in Poland.