Primary Objective: Deliver High-Quality Site Monitoring Services
We are seeking experienced Contract Research Associates to ensure timely and qualitative site monitoring activities in accordance with our Site Monitoring Plan.
Main Responsibilities:
* Demonstrate comprehensive understanding of the Site Monitoring Master Plan, study protocol, and project plan to guarantee adherence to quality and timelines.
* Manage sites in compliance with the Site Monitoring Master Plan and relevant regulations to minimize Quality Assurance audit observations.
* Identify new potential sites within various therapeutic areas to expand our clinical network.
* Engage in continuous skill development, applying technical and soft skills to enhance performance and project outcomes.
Key Performance Indicators:
* Timely and high-quality execution of site monitoring activities.
* Prompt report generation and submission to stakeholders.
Essential Skills and Qualifications:
* Education: Bachelor's or Master's degree in a scientific discipline.
* Experience: 1-4 years of experience in site monitoring within clinical research.
* Skills: Strong understanding of ICH GCP and applicable clinical trial regulations; excellent verbal and written communication; ability to multitask and thrive under demanding timelines.