The Site Coordinator is responsible for the effective management and conduct of clinical trials under the supervision of the Principal Investigator. This role includes planning daily activities and ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). Facilitates communication between the clinical trial site, sponsor, and internal and external stakeholders, ensuring the secure collection of study data, protection of subject safety, and compliance with regulatory authorities.  

The Business Analyst supports the organization’s strategic objectives by conducting data-driven analyses that enhance internal processes and drive market-oriented growth strategies. This role collaborates cross-functionally to monitor key performance indicators, generate insights, and contribute to informed decision-making. The Business Analyst also supports research activities in areas such as pricing, regulatory analysis, and cost-benefit evaluations.