Regulatory Site Management Associate I – Warsaw

ICON Clinical Research; Warszawa; On-site; PLN 52,000 - 76,000; Full time

Benefits offered by this job

Annual leave

Health insurance

Retirement planning

Employee assistance program

Job summary

ICON Strategic Solutions in Warsaw, Poland, is seeking a Site Management Associate I (Regulatory) to support monitoring of clinical trial sites and ensure adherence to study protocols and GCP guidelines.

You will collaborate with cross-functional teams, manage documentation, and help prepare monitoring reports, while traveling approximately 25% of the time. Bachelor's degree in life sciences or related field is required.

Qualifications

• Bachelor's degree required in life sciences or related field.
• Experience in clinical research or site management is preferred but not mandatory.
• Strong organizational and communication skills are essential.

Responsibilities

• Assist in monitoring of clinical trial sites and adherence to protocols.
• Support site management activities including documentation and data entry.
• Collaborate with cross-functional teams to resolve site-related issues.
• Maintain accurate records of site activities and monitoring reports.
• Participate in ongoing training to enhance trial management skills.

Skills

Excellent communication skills

Strong organizational skills

Attention to detail

Team player

Willingness to travel

Education

Bachelor's degree in life sciences or related field

Job description

ICON Strategic Solutions in Warsaw, Poland, is seeking a Site Management Associate I (Regulatory) to support monitoring of clinical trial sites and ensure adherence to study protocols and GCP guidelines.

You will collaborate with cross-functional teams, manage documentation, and help prepare monitoring reports, while traveling approximately 25% of the time. Bachelor's degree in life sciences or related field is required.