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Precision Medicine Group
Start Up Specialist
Remote · Hungary, Poland + more · Full time · Mid level
About the role
Join as a Start Up Specialist to support clinical trial start-up activities across multiple countries. Manage submissions, communications, and regulatory compliance for clinical trials.
What you’ll do
• Prepare Clinical Trial Application Forms and submission dossiers. • Interact with Competent Authorities and Ethics Committees. • Maintain project plans and regulatory intelligence tools. • Customize patient information and consent forms. • Support site activation and document collection.
What you’ll bring
• Bachelor’s degree in life sciences or related field. • Experience as Regulatory or Start Up specialist in CRO or pharma. • Fluent in Hungarian and English. • Strong communication and organizational skills. • Experience with computerized information systems.
Life at Precision Medicine Group
Equal Opportunity Employer with commitment to diversity and inclusion. Support for applicants with disabilities.
About Precision Medicine Group
Precision Medicine Group enables precision medicine through clinical trial design, operational expertise, and biomarker analytics focused on rare diseases and oncology.