💼 About This Role

You'll monitor clinical studies at investigative sites in Bulgaria, ensuring compliance with protocols and regulations. You'll coordinate site setup activities and support project managers on larger trials. This role offers lower travel and higher work-life balance compared to industry averages.

🎯 What You'll Do

• Monitor clinical studies at investigative sites for compliance with protocols and regulations.
• Coordinate site setup activities including investigator identification and regulatory submissions.
• Support project managers on larger-scope clinical trials.
• Train and mentor junior clinical research staff.

📋 Requirements

• 3+ years of CRA experience in CRO or pharmaceutical industry.
• Availability for domestic travel up to 50-60%.
• Fluency in Serbian, English, and Bulgarian languages.
• 4-year college degree or equivalent experience.