CRA II

Description

• Site monitoring from site selection to study close out
• Monitor the progress of assigned clinical trials and escalate any protocal deviation, SAE, risk to timely completion of study milestones
• Submit monitoring visit report to Clinical Trial Manager on time
• Cross functional collaboration with site staff, PI, CTM, CTA, contracts and SSU team
• Monitoring in global oncology studies, including on site and remote monitoring visit
• Approx 50% travel, hybrid office based

Qualifications

• Tertiary degree qualified in Life Sciences
• 2+ years independent site monitoring experience
• Ideally previous exposure to Oncology trials
• Excellent communication and presentation skills
• Experience working within CRO/Pharma industry is essential