Dally J.

Led the planning, initiation, and execution of clinical trials in compliance with international regulations, ICH-GCP guidelines, and company SOPs Managed third-party vendors (e.g., central labs, imaging) to support trial activities, ensuring they adhered to quality standards and timelines Collaborated with data management teams to ensure accurate and timely data collection, cleaning, and database lock Oversaw the timely reporting of adverse events and serious adverse events to regulatory authorities and sponsors Reviewed site visit reports and ensured monitoring (i.e., scheduling and scope) was executed per the clinical monitoring plan and that all protocol deviations were accurately logged Prepared study sites and study teams for internal and external audits and regulatory inspections Maintained regular communication with sponsors, addressing their concerns and providing updates on trial progress.

Coordinated and managed daily clinical trial activities per study protocols. Recruited, screened, and enrolled study participants. Obtained informed consent from study participants. Ensured accurate and timely data entry and documentation. Monitored participants for adverse events and reported findings to investigators. Scheduled and conducted study visits and follow-ups with monitors. Maintained regulatory binders and ensured compliance with regulatory requirements.

• Ensured the accurate and timely dispensing of prescription medications to patients, maintaining a 99% accuracy rate. • Managed inventory and stock levels, reducing overstock and minimizing expired medications by 15%. • Collaborated with healthcare providers to optimize patient care through medication therapy reviews, leading to improved patient outcomes. • Supported the implementation of pharmacy services to enhance patient care and improve operational efficiency. • Maintained compliance with pharmacy regulations and quality standards, ensuring a safe and efficient pharmacy operation.