- Providing freelance site monitoring services for multiple clinical studies across diverse therapeutic areas with a particular focus on oncology, ensuring compliance with GCP and regulatory requirements- Collaborating with investigators and site staff to resolve issues, ensuring smooth conduct of clinical trials.- Delivering customized monitoring services tailored to sponsor requirements, leveraging experience with global CROs and local expertise.- Supporting regulatory submissions by ensuring timely and accurate collection of essential site documents for Ethics Committee and Competent Authority approvals

- Under ClinOps Model, working with multiple sponsors- Research Areas of Oncology, Thoracic Diseases- Managing 18 sites in 3 different studies, with different indications with varying phases from II to IV

Under FSP model of IQVIA, dedicated to the single sponsor of Alexion Pharmaceuticals Inc. / AstraZeneca Rare Disease Unit. Coordinated and scheduled protocol-related visits and requiredtesting to demonstrate vigilance in patient safety, protocol compliance and data quality. Assisted in investigator selection and qualification process to provide capable investigators with adequate resources to properly conduct trials. Set up, initated and activated trial study centers to manageclinical study activities for 20 sites across 4 different studies.