This is a fully remote position, open to applicants in Poland.

📋 Description

• Accountable for overseeing remote site monitoring tasks to guarantee that sites are executing the study(ies) and submitting study data in accordance with the study protocol, relevant regulations and guidelines, and the sponsor's expectations.

• May engage in on-site monitoring and/or co-monitoring as required.

• Conducts Site Identification (Site ID) and/or Site Start-Up (SSU) activities as necessary.

• Collaborates effectively with various functional teams, including Clinical Operations Lead (COL), Project Management, Regulatory Start-Up (RSU), and Epidemiology.

• Completes the necessary therapeutic, protocol, and clinical research training to fulfill job responsibilities.

⛳️ Requirements

• 2 - 3 years of relevant prior experience.

• Intermediate understanding of the principles, theories, and concepts within the job area, typically acquired through advanced education complemented by experience.