Sites Coordinator Role Overview
As a Sites Coordinator, you will be responsible for ensuring the timely and qualitative delivery of site monitoring activities. Your primary objective will be to manage sites according to the Site Monitoring Master Plan (SMMP) and relevant regulations to minimize Quality Assurance (QA) audit observations.
Key Responsibilities:
* Gain comprehensive understanding
* Ensure adherence to quality and timelines
* Manage sites according to SMMP and regulations
* Identify new potential sites within various therapeutic areas
* Enhance technical and soft skills
Work Relations:
* Report to Manager of Clinical Operations
* Collaborate with site monitoring team and site personnel
Value Added:
Your adherence to the quality and timelines of the monitoring plan will be crucial for the efficient delivery of our projects and overall success.
Essential Skills Experience:
* Bachelor's or Master's degree in a scientific discipline
* 1-4 years of experience in site monitoring within clinical research
* Strong understanding of ICH GCP and applicable clinical trial regulations
* Excellent verbal and written communication
* Ability to multitask and thrive under demanding timelines