**Job Title:** Clinical Research Associate
We are seeking a skilled Clinical Research Associate to ensure the timely and qualitative delivery of site monitoring activities.
Responsibilities:
* Deliver on the Site Monitoring Plan: Gain a comprehensive understanding of the Site Monitoring Master Plan, study protocol, and project plan to ensure adherence to quality and timelines.
* Site Management Compliance: Manage sites according to the Site Monitoring Master Plan and relevant regulations to minimize Quality Assurance audit observations.
* Site Identification: Assist in identifying new potential sites within various therapeutic areas to expand our clinical network.
* Continuous Skill Development: Regularly enhance both technical and soft skills, applying them to elevate performance and project outcomes.
Key Qualifications:
* 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.