As a Clinical Trial Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. **What You Will Be Doing:** + Assisting in the monitoring of clinical trial sites, ensuring adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. + Supporting site management activities, including documentation preparation, data entry, and tracking site performance metrics. + Collaborating with cross-functional teams to facilitate communication and address site-related issues effectively. + Maintaining accurate records of site activities and contributing to the preparation of monitoring reports. + Participating in training and development initiatives to enhance knowledge and skills in clinical trial management. **You Are** + Bachelor’s degree in a relevant field such as life sciences, healthcare administration, or clinical research is highly preferred. + Some experience in clinical research, site management, or related administrative roles is preferred but not mandatory. + Strong organizational skills and attention to detail, with the ability to manage multiple tasks effectively. + Basic knowledge of clinical trial processes and regulatory requirements is a plus. + Excellent communication and interpersonal skills, with the ability to work collaboratively within a team environment.