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Precision Medicine Group
Cra II/ Scra
Remote · Poland · Full time · Mid level
About the role
Manage and monitor investigative sites independently from initiation through close-out. Ensure study compliance with protocols, SOPs, and regulatory requirements.
What you’ll do
• Manage and monitor investigative sites independently. • Partner with CTMs and study teams to resolve issues. • Ensure studies comply with protocol and regulations. • Interact with clients and support site payments. • Mentor less experienced CRAs and contribute expertise.
What you’ll bring
• 3+ years independent monitoring experience. • Experience in oncology clinical trials. • Availability for up to 60% domestic travel. • Fluency in Polish and English. • Graduate degree in scientific or healthcare discipline preferred.
Life at Precision Medicine Group
High CRA retention rates and a smaller CRO environment with autonomy. Supportive culture valuing employee contributions.
About Precision Medicine Group
Precision Medicine Group specializes in precision medicine, combining clinical trial design, biomarker analytics, and expertise to advance cancer therapies.