Remote Clinical Research Associate II (Poland)

Premier Research Group; Polska; Remote; PLN 128,000 - 170,000; Full time

Benefits offered by this job

Health insurance

Retirement plan

Paid time off

Employee Assistance Program

Job summary

Premier Research is seeking a Clinical Research Associate II in Poland to join our Clinical Monitoring, Site Management and SSU team. The role may be fully remote, ideally based in central Poland, and offers a path to grow within a globally respected CRO.

You will monitor trials to ensure data integrity and patient safety, manage TMF/eTMF, and coordinate site activities across Phase II/III studies with diverse therapeutic areas.

Qualifications

• Undergraduate degree or its international equivalent in clinical, science, or health-related field
• A licensed health-care professional or equivalent work experience
• At least 1 year of independent monitoring experience
• Experience in Neurology, Oncology, or Dermatology preferred
• Experience supporting Phase II & III studies

Responsibilities

• Delivers quality, timely monitoring reports for sponsor approval per plan timelines
• Maintains expenses submission per travel guidelines
• Monitors remotely or onsite with focus on data integrity and patient safety
• Plans day-to-day monitoring activities and prioritizes sites
• Prepares for on-site visits and conducts qualification, initiation, interim, and close-out monitoring
• Maintains TMF/eTMF per guidelines and understands essential documents per ICH/GCP
• Reviews site documents for accuracy and completeness

Skills

Clinical monitoring

Data integrity

Patient safety

Regulatory compliance

Education

Bachelor's degree in clinical/science/health-related field

Tools

eTMF

ICH/GCP

Job description

Premier Research is seeking a Clinical Research Associate II in Poland to join our Clinical Monitoring, Site Management and SSU team. The role may be fully remote, ideally based in central Poland, and offers a path to grow within a globally respected CRO.

You will monitor trials to ensure data integrity and patient safety, manage TMF/eTMF, and coordinate site activities across Phase II/III studies with diverse therapeutic areas.