Senior Clinical Research Associate

• Monitor and own the progress of clinical studies at investigative sites
• Ensure clinical studies are conducted, recorded, and reported according to protocol, SOPs, ICH-GCP, applicable regulations, and standards
• Coordinate activities required to set up and monitor studies
• Identify investigators
• Help prepare regulatory submissions
• Conduct pre-study and initiation visits
• Handle appropriately sized clinical trials
• Support Project Managers on larger-scope trials
• Train and mentor junior staff members
• Interact directly with clients
• Initiate payments
• Participate in proposal activities, including development and client presentations

• 4-year college degree or equivalent experience
• 3+ years of independent monitoring experience within the CRO or pharmaceutical industry
• Experience managing oncology studies
• Availability for domestic travel including overnight stays, approximately 50–60% travel commitment
• International travel may be required for some senior-level positions
• Fluency in Polish and English
• Candidates must be legally authorized to work in the country of employment without employer sponsorship
• Preferred: graduate or postgraduate degree in a scientific or healthcare discipline
• Preferred: experience managing CAR-T/phase I studies
• Preferred: study start-up activities experience
• Preferred: understanding of financial management

• Fully home-based work option
• Reasonable travel and improved work/life balance
• Direct line management support
• Opportunity to train and mentor junior staff members
• Employee input and ideas valued and nurtured
• Equal opportunity employment
• Reasonable accommodation support during the application process