Site Monitoring Associate
We are seeking a skilled Site Monitoring Associate to ensure the timely and qualitative delivery of site monitoring activities in alignment with our Site Monitoring Plan (SMP).
Gain a comprehensive understanding of the SMS Master Plan, study protocol, and project plan to ensure adherence to quality and timelines.
1. Deliver on the SMS Master Plan: Conduct thorough reviews of the master plan to identify areas for improvement and implement changes as needed. Ensure that all site staff are trained on the revised plan.
2. Manage Sites: Oversee the management of sites according to the SMS Master Plan and relevant regulations to minimize Quality Assurance (QA) audit observations.
3. Identify New Sites: Assist in identifying new potential sites within various therapeutic areas to expand our clinical network.
Requirements:
* 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 skills.