Perform site monitoring visits in accordance with contracted scope of work and regulatory requirements
Work with sites to adapt, drive, and track subject recruitment plan
Administer protocol and related study training to assigned sites
Evaluate the quality and integrity of study site practices
Manage the progress of assigned studies by tracking regulatory submissions and approvals
Ensure documentation regarding site management is maintained
Collaborate and liaise with study team members for project execution support

Requires at least 12 months independent on-site monitoring experience of interventional studies
Experience across start-up, enrolment, maintenance, close-out
Digital literacy, including confidence using AI tools
Degree in scientific discipline / health care or equivalent industry experience
Good knowledge of GCP and ICH guidelines
Ability to establish and maintain effective working relationships

Clinical Research Associate II

Key skills