Engage in structured training program to gain knowledge and skills
Conduct site monitoring visits (selection, initiation, monitoring and close out visits)
Administer protocol and related study training to assigned sites
Evaluate the quality and integrity of study site practices
Manage the progress of assigned studies
Ensure availability of site documents for filing in the TMF
Create and maintain documentation regarding site management and monitoring visit findings

Requirements

A Bachelor's degree in a health care or other scientific discipline or educational equivalent
Prior clinical experience preferred
Advanced knowledge of applicable clinical research regulatory requirements (GCP and ICH guidelines)
Computer skills including proficiency in Microsoft Word, Excel, PowerPoint
Written and verbal communication skills including good command of Polish and English

Benefits

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

clinical researchsite monitoringprotocol administrationstudy evaluationdocumentation managementregulatory requirementsGCP guidelinesICH guidelines

communication skillswritten communicationverbal communicationorganizational skills