Assistant Clinical Research Associate

Job Summary

A company is looking for an Assistant CRA.

Key Responsibilities

• Completes study and site management activities as defined in the task matrix
• Supports site management and remote monitoring tasks in accordance with SOPs and regulatory guidelines
• Coordinates study/site supply management and logistics throughout the study phases

Required Qualifications

• 1 to 2 years of relevant experience or a combination of education and training
• Basic medical/therapeutic area knowledge and understanding of medical terminology
• Ability to work independently or as part of a team
• Advanced digital literacy, particularly with MS Office
• Knowledge of ICH GCP and applicable regulations