Experienced professional with over 5.5 years in Clinical Operations and Central Monitoring, specializing in multi-phase clinical trials across diverse therapeutic areas, demonstrates robust expertise in regulatory compliance, site monitoring, and project management within Pharmaceutical and CRO settings. Holds a Bachelor of Pharmacy, augmenting clinical understanding with a strong foundation in pharmacy sciences. Skilled in handling critical functions such as CAPA tracking, deviation management, and compliance tracking while ensuring adherence to international standards and protocols. Proficient in multiple clinical data management systems and regulatory frameworks, complemented by proven stakeholder collaboration and mentoring abilities within high-stakes environments. Career objectives center on leveraging clinical and operational insights to enhance trial efficiency and data integrity in challenging roles.
· Collaborating with stakeholders in the Medical Content Approval (MCA) process as a reviewer and approver of crucial medical content
· Leading the migration projects for Adobe Experience Manager (AEM)
· Developing Permission Managed Content (PMC) to ensure regulatory compliance and content security
· Conducting training sessions and providing mentorship to enhance team capabilities and performance