Provide site support to study teams and ensure regulatory compliance (ICH/GCP, GPP).
Coordinate investigator site files and document management.
Schedule internal and external meetings and manage logistics.
Maintain data in CTMS and ensure timely EDC data entry.
Serve as site liaison for inquiries and issue escalation.
Assist with site visits and remote review of documents.

🎯 Requirements

Bachelor's degree or international equivalent in healthcare/science.
Minimum of 2 years of relevant clinical research experience.
MS Office proficiency (Outlook, Word, Excel, PowerPoint).
Fluent in Serbian and English (written and spoken).
Working knowledge of the drug development process.
Ability to travel as needed.

🎁 Benefits

Remote work environment.
Equal Opportunity Employer.

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