Florin Popilean

Managed end-to-end clinical research projects in multiple therapeutic areas according to time, quality/scope, and cost constraints. Oversaw clinical research conduct, acted as a liaison with the client, and managed contractual deliverables and modifications. Communicated project status, escalated issues, and troubleshooted to ensure client satisfaction.

• Successfully delivered 5 clinical trials resulting in a 95% sponsor satisfaction rate

• Managed cross-functional teams and third-party vendors, ensuring timely project delivery and adherence to local regulations, ICH GCP guidelines, SOPs, and project-specific plans

• Prepared and delivered study-related updates, dashboards, and reports to study teams, senior management, and sponsors/vendors/partners

Coordinated and managed clinical trial activities in compliance with local regulations, ICH GCP guidelines, and study-specific protocols. Worked with cross-functional teams to ensure successful project delivery and client satisfaction. Collaborated with investigators and research coordinators to ensure efficient conduct of clinical trials.

• Managed clinical trial conduct, including study start-up, enrollment, execution, and close-out resulting in a 90% patient retention rate

• Collaborated effectively with internal and external stakeholders, communicated project status, escalated issues, and troubleshooted

• Managed study-related essential documents, coordinated IRB/IEC correspondence and communication, and ensured that study supplies and equipment were procured and delivered to patients and/or sitesCoordinated and managed clinical trial activities in compliance with local regulations, ICH GCP guidelines, and study-specific protocols. Worked with cross-functional teams to ensure successful project delivery and client satisfaction. Collaborated with investigators and research coordinators to ensure efficient conduct of clinical trials.

• Managed clinical trial conduct, including study start-up, enrollment, execution, and close-out resulting in a 90% patient retention rate

• Collaborated effectively with internal and external stakeholders, communicated project status, escalated issues, and troubleshooted

• Managed study-related essential documents, coordinated IRB/IEC correspondence and communication, and ensured that study supplies and equipment were procured and delivered to patients and/or sites

Managed and coordinated clinical research studies, including subject recruitment and screening, data collection and analysis, and regulatory compliance.

Collaborated with investigators, research staff, and study sponsors to ensure the successful conduct of clinical trials. Assisted in the development and implementation of study protocols and procedures.

• Coordinated and managed clinical research studies, resulting in a 80% enrollment rate

• Assisted in the development and implementation of study protocols and procedures

• Maintained study-related essential documents and ensured compliance with regulatory requirements