CRA II: Clinical Research Monitor (Remote & Onsite)

Emmes; Warszawa; Hybrid; PLN 120,000 - 170,000; Full time

Job summary

Emmes Group seeks a Clinical Research Associate II to monitor clinical study sites onsite or remotely. You will conduct visits, review informed consent and source data, ensure compliance with protocol and ICH GCP, and prepare site visit reports. Training site staff and coordinating with project teams are part of the role.

The position emphasizes collaboration, attention to detail, and adaptability across multiple studies and sites, with focus on global health impact.

Qualifications

• Bachelor's Degree in a scientific field or equivalent work experience.
• 2-3 years of on-site or remote monitoring experience.
• Proficiency with MS Office Suite and strong computer skills.
• Excellent organizational and communication skills, both oral and written.
• High attention to detail and ability to work on multiple projects.
• Self-starter, team player, and capable of cross-functional work with oversight.
• Knowledge of clinical research operations and country regulations.
• Strong problem solving, adaptability, and time management.

Responsibilities

• Schedule and conduct remote and on-site monitoring visits.
• ICF review, source data verification, and regulatory compliance reviews.
• Document observations in site visit reports.
• Facilitate action item resolution post-visit.
• Ensure visits comply with protocol, SOPs, ICH GCP and regulatory requirements.
• Provide training to site staff.
• Identify follow-up needs and report findings to supervision.
• Serve as contact for study site personnel and resolve issues.
• Assist with audits preparation and support.
• Coordinate study supplies and regulatory submissions.
• Participate in Investigator Meetings and project team meetings.
• Archive study documents and maintain records.
• Ensure adherence to policies and standards.

Education

Bachelor's Degree in Scientific discipline

Tools

MS Office Suite

Job description

Emmes Group seeks a Clinical Research Associate II to monitor clinical study sites onsite or remotely. You will conduct visits, review informed consent and source data, ensure compliance with protocol and ICH GCP, and prepare site visit reports. Training site staff and coordinating with project teams are part of the role.

The position emphasizes collaboration, attention to detail, and adaptability across multiple studies and sites, with focus on global health impact.