Knowledge of good clinical practice gcp guidelines
This structured training program prepares candidates to independently conduct clinical monitoring visits in accordance with study protocols and regulatory requirements
Job Summary
This structured training program prepares candidates to independently conduct clinical monitoring visits in accordance with study protocols and regulatory requirements.
The role involves performing site monitoring visits, managing study progress, and ensuring the quality and integrity of site practices under close supervision.
Candidates will collaborate with study teams to support project execution, manage recruitment plans, and maintain essential trial documentation.
Matching Summary
This structured training program prepares candidates to independently conduct clinical monitoring visits in accordance with study protocols and regulatory requirements.
Skills & Requirements
Must-have
Bachelor's Degree in scientific discipline
Proficiency in Microsoft Word Excel PowerPoint
Knowledge of Good Clinical Practice GCP guidelines
Nice-to-have
Prior clinical research experience preferred
Strong written and verbal English communication skills
Ability to establish effective working relationships
Key Requirements
Bachelor's Degree in scientific or healthcare field
2 years clinical experience (if required by organization)