CRA II/ SCRA

The role

You will independently manage and monitor investigative sites from initiation through close-out. You will partner with CTMs and study teams to ensure studies follow protocols, SOPs, ICH-GCP, and regulatory requirements.

What you will do

• Independently manage and monitor investigative sites
• Take ownership of site performance, quality and risk identification
• Partner with CTMs and study teams to anticipate issues and drive resolution
• Ensure studies are conducted, recorded and reported in accordance with protocol, SOPs, ICH-GCP and regulatory requirements
• Interact directly with clients
• Support site payment activities
• Mentor less experienced CRAs
• Contribute to study-level discussions and process improvements

Required qualifications

• 3+ years of independent monitoring experience within the CRO or pharmaceutical industry
• Independent monitoring experience in oncology clinical trials
• Availability for domestic travel, including overnight stays, which may constitute up to approximately 50–60% travel commitment
• Occasional international travel may be required
• Fluency in Polish and English

Nice to have

• 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

Before you apply

• Candidates must be legally authorized to work in the country of employment without employer sponsorship
• Please, apply in English

About the company

Precision for Medicine is a CRO that combines novel clinical trial designs, operational and medical experts, and advanced biomarker and data analytics solutions. The company focuses on precision medicine, rare diseases, and oncology.