In-House Clinical Research Associate (Poland)

Site Management:

• Serve as contact for project team and investigative sites.
• Manage and file site specific documents in (e) TMF.
• Monitor site performance and implement action plans.

General Monitoring Responsibilities:

• Perform onsite visits as co-monitor if needed.
• Supports preparation for audit and required follow-up actions.

Site Setup and Startup Support:

• Support patient recruitment providing guidance to site teams of inclusion/exclusion criteria.
• Coordinate the movement and delivery of trial materials, samples, tests, and forms.

Training and Development:

• Support and observe primary assigned CRAs at both onsite and remote visits.
• Participate in all study related activities, including training, team meetings and provide any necessary updates to the study team.