• Managed theranostic oncology research projects, ensuring protocol adherence and regulatory compliance.• Coordinated IRB submissions and facilitated communication between research teams and regulatory bodies.• Collected and maintained accurate research data, monitoring patient outcomes and treatment responses.

• Manage the onboarding process of new employees and provide employee training to ensure a fast and smooth integration into the new function, maximizing the performance output. • QA multiple problem trials and successfully returned to excellent standing with the CRO.• Complete all forms and correspondence and reports to the CROs and sponsors in a timely manner.• Screen, enroll and follow study subjects ensuring protocol compliance and close monitoring while the subjects are on the study. • Responsible for all data collection, source documentation, developing/completing study-specific case report forms and submission of adverse experience reports. • Create study specific tools for source documentation when not provided by the sponsor.• Ensure compliance with protocol guidelines and requirements of regulatory agencies; identify problems and/or inconsistencies and monitor patients progress to include documentation and reporting of adverse events; recommend corrective action as appropriate.• Initiate studies, screen patients for study eligibility to participate as per protocol, inclusion/exclusion criteria and informed consent process. • Submit SAE reports and supporting documents. • Coordinated study protocols, schedule and perform visits, and perform drug accountability and subject recruiting