Specialist/Snr Specialist Study Start Up and Regulatory Affairs
Ergomed · Other
Forrás: Himalayas
This role’s source listing does not include Hungary as an eligible location.
The Senior Specialist coordinates study start-up and regulatory affairs activities within Czechia, ensuring compliance and timely delivery of clinical milestones.
This role manages regulatory documentation, clinical site agreements, and study initiation readiness for medium-complexity projects. You will act as a key liaison between internal teams and external stakeholders, providing strategic regulatory input while maintaining compliance with ICH-GCP standards.
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A cégről
Ergomed is a specialist clinical research organization focusing on rare disease and oncology indications. They partner with small to mid-sized biotech companies to facilitate clinical trials and drug development globally.