Conversion Rate Optimizer

• Monitor the progress of clinical studies at investigative sites or remotely
• Ensure clinical trials are conducted, recorded, and reported according to the protocol, SOPs, ICH-GCP, and applicable regulatory requirements
• Conduct site qualification, initiation, monitoring, and close-out visits according to the monitoring plan and applicable guidelines
• Participate in investigators’ meetings
• Prepare site visit reports and follow-up letters to investigators
• Build productive relationships with investigators and site staff to achieve study objectives and patient recruitment targets
• Perform source data verification
• Ensure on-site study drug storage, dispensing, and accountability are adequate
• Ensure data collection and regulatory document collection are adequate
• Take on other responsibilities when appropriately experienced, qualified, and/or trained

Conversion Rate Optimizer jobs in Australia

Freelance CRA, Dermatology/Rheumatology