International conference on harmonization (ich) guidelines
Site monitoring visit execution
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Ivivamedical is seeking an experienced Clinical Research Associate in Israel to handle site monitoring and management tasks, ensuring compliance with study protocols and regulations. The ideal candidate should have at least two years of on-site monitoring experience and possess strong organizational and communication skills.
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Job Summary
The role involves performing site monitoring visits including selection, initiation, monitoring, and close-out in accordance with regulatory requirements.
Candidates must work with sites to adapt and drive subject recruitment plans while ensuring the integrity of study data.
The position requires maintaining accurate documentation for the Trial Master File and Investigator's Site File according to GCP standards.
Matching Summary
Match Score: 75
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Ivivamedical is seeking an experienced Clinical Research Associate in Israel to handle site monitoring and management tasks, ensuring compliance with study protocols and regulations. The ideal candidate should have at least two years of on-site monitoring experience and possess strong organizational and communication skills.
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Skills & Requirements
Must-have
Good Clinical Practice (GCP) knowledge
International Conference on Harmonization (ICH) guidelines
Site monitoring visit execution
Subject recruitment plan management
Trial Master File maintenance
Nice-to-have
Strong organizational and problem-solving skills
Effective time and financial management
Proficiency in Microsoft Office suite
Ability to establish client relationships
Key Requirements
At least 2 years of on-site monitoring experience
High School Diploma or equivalent Degree in scientific discipline