Deanna Plummer Email & Phone Number

Spring Lake, Nc, Us

Raleigh-Durham-Chapel Hill Area

In my role as a Clinical Site Activation Specialist at IQVIA, I have played a pivotal role in expediting the initiation phase of clinical trials. Leveraging my in-depth understanding of regulatory requirements and industry guidelines, I have been responsible for orchestrating the timely activation of clinical sites. This has involved meticulous coordination with investigative sites, overseeing the compilation and submission of essential documents to regulatory authorities, and ensuring compliance with Institutional Review Board (IRB) protocols. I have successfully streamlined site activation processes by developing and maintaining standardized templates for regulatory submissions, fostering efficiency and consistency across multiple studies. Collaborating closely with cross-functional teams, including project managers, clinical research coordinators, and regulatory affairs professionals, I have facilitated open lines of communication to address challenges and mitigate delays. Additionally, my role has entailed conducting training sessions for site personnel, ensuring a comprehensive understanding of study protocols and regulatory requirements. Through my dedication to detail and efficient project management, I have contributed to the successful activation of clinical sites, ultimately supporting the overall progress and success of diverse clinical research initiatives at IQVIA.

Honolulu, Hawaii, United States

As a Clinical Research Coordinator at Hawaii Pacific Neuroscience, I have successfully managed and coordinated multiple clinical trials throughout their life cycles. With a keen understanding of regulatory compliance, I have ensured the timely submission of all required documentation to the Institutional Review Board (IRB), facilitating the seamless initiation and execution of studies. My responsibilities have encompassed participant recruitment, screening, and enrollment, where I have consistently maintained the highest standards for informed consent processes. Working collaboratively with cross-functional teams, including principal investigators, physicians, and study sponsors, I have fostered an environment of effective communication and teamwork. In addition, I have overseen the development and maintenance of comprehensive study documentation, including source documents and regulatory binders, ensuring accuracy and adherence to protocol requirements. Conducting monitoring visits and audits to guarantee protocol adherence and data accuracy, I have implemented and maintained electronic data capture (EDC) systems to streamline data management processes. Furthermore, my role has involved meticulous budget management, tracking expenses, and coordinating payments to vendors, contributing to the financial efficiency of each study. Overall, my experience and commitment position me as a valuable asset in facilitating the success of clinical research initiatives.

Master'S Degree, Psychology

Bachelor Of Science - Bs, Biology, General

Bachelor Of Arts - Ba, Psychology