Site Activation & Regulatory Docs Specialist

ICON; Warszawa; On-site; PLN 163,000 - 237,000; Full time

Job summary

A leading healthcare intelligence organization is seeking a FSA-Site Specialist to support site activation tasks and manage critical regulatory documents. The role involves collaboration with Site Partners, ensuring compliance with regulations, and maintaining high standards of quality. Candidates should have a Bachelor's degree and 3-6 years of clinical research experience. The position offers a competitive salary and a range of benefits in Warsaw, Poland.

Benefits

Annual leave entitlements

Health insurance offerings

Retirement planning

Employee Assistance Programme

Flexible optional benefits

Qualifications

• 3-6 years of experience in a Clinical Research environment.
• Ability to support other Site Specialists as needed.
• Demonstrate ability to identify study and site risks.

Responsibilities

• Support preparation and tracking of regulatory documents.
• Collaborate with Site Partners for successful site activation.
• Ensure accuracy of the Critical Document Package.

Skills

Organizational skills

Task prioritization

Communication skills

Education

Bachelor's Degree

Tools

Microsoft Office

Job description

A leading healthcare intelligence organization is seeking a FSA-Site Specialist to support site activation tasks and manage critical regulatory documents. The role involves collaboration with Site Partners, ensuring compliance with regulations, and maintaining high standards of quality. Candidates should have a Bachelor's degree and 3-6 years of clinical research experience. The position offers a competitive salary and a range of benefits in Warsaw, Poland.