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Precision for Medicine is a specialized CRO focused on precision medicine, biomarker-driven clinical trials, and oncology research. The company is known for high CRA retention rates and a culture that values autonomy, manageable study portfolios, and reasonable travel expectations.
You will independently manage and monitor investigative sites throughout the clinical trial lifecycle, from initiation through close-out. Your responsibilities include:
• Independently monitor investigative sites, taking ownership of site performance, quality, and risk identification
• Partner closely with Clinical Trial Managers (CTMs) and study teams to anticipate issues and drive timely resolution
• Ensure studies are conducted, recorded, and reported in accordance with protocol, SOPs, ICH-GCP, and applicable regulatory requirements
• Identify emerging risks early, escalate appropriately, and bring solutions to the table
• Build credible relationships with investigators and site teams while confidently addressing difficult or sensitive issues
• Manage competing priorities across your sites without compromising quality
• Communicate clearly with CTMs and study teams, representing the site perspective in project discussions
• Interact directly with clients and support site payment activities
• Depending on experience, mentor less experienced CRAs and contribute expertise to study-level discussions and process improvements
Precision for Medicine combines novel clinical trial designs, industry-leading operational and medical expertise, advanced biomarker and data analytics solutions, and deep specialization in rare diseases and oncology. The company is revolutionizing cancer research by using biomarkers to link specific mutations to specific treatments and designing targeted, adaptive clinical trials.
This is a fully home-based position with significant travel requirements (50–60% domestic travel with occasional overnight stays and potential international travel).
**Requirements:**
Minimum Required:
• 3+ years of independent monitoring experience within a CRO or pharmaceutical industry
• Independent monitoring experience in oncology clinical trials
Other Required:
• Availability for domestic travel, including overnight stays (approximately 50–60% travel commitment); occasional international travel may be required
• Fluency in Polish and English
Preferred:
• Graduate or postgraduate degree with a concentration in a scientific or healthcare discipline
• Experience monitoring complex early-phase oncology studies, including Phase I and/or CAR-T trials
