Clinical research professional with extensive experience in clinical trial management, specializing in the coordination of trials for surgical specialties and research in aging outpatient populations. Key expertise includes:✔ Designing and developing versatile RedCap databases, ranging from simple to complex longitudinal studies.✔ Creating and customizing data entry forms (trial-specific case report forms).✔ Comprehensive project management, ensuring meticulous oversight from initiation to completion✔ Maintaining regulatory compliance throughout clinical trial management.✔ Prioritizing clear and regular communication throughout the project lifecycle.

In my role as a Clinical Research Coordinator, I specialize in managing studies from inception to completion, particularly within surgical specialties, covering both inpatient and surgical outpatient populations with in-clinic recruitment. Collaborating closely with investigators, I contribute to the setup of new studies, maintain ongoing studies, and ensure regulatory compliance. Additionally, I foster comprehensive collaboration between sponsors, other departments, and university collaborators to facilitate seamless coordination throughout the entire study lifecycle.✔ Oversee studies from setup to maintenance with meticulous attention to detail.✔ Develop and implement recruitment strategies tailored to surgical inpatients and outpatient populations.✔ Facilitate seamless collaboration between sponsors, departments, and university collaborators for effective study coordination.✔ Ensure accurate and timely entry of participant data into study databases.✔ Adhere to and maintain a high standard of regulatory compliance throughout the study lifecycle.✔ Train, lead, and guide a team of coordinators in executing study objectives.✔ Develop and refine processes to enhance study efficiency.✔ Contribute to the strategic planning of study initiatives for various clinical trials.