Sara E. Email & Phone Number

As a dedicated professional with extensive experience in clinical research coordination and trial management, I have consistently demonstrated my commitment to ensuring the highest standards of quality and compliance. With a proven track record as a Lead Clinical Research Coordinator and experienced Clinical Trial Assistant, I bring a wealth of expertise to every project I undertake.In my previous role as a Lead Clinical Research Coordinator, I spearheaded the coordination of numerous clinical trials, overseeing all aspects of study implementation from initiation to closeout. My responsibilities included protocol development, participant recruitment and enrollment, regulatory compliance, and data collection and management. Leveraging my strong organizational skills and attention to detail, I successfully managed multiple concurrent trials, ensuring adherence to study timelines and objectives.Additionally, I have substantial experience in managing Electronic Trial Master File (eTMF) systems, playing a pivotal role in maintaining document integrity and compliance throughout the trial lifecycle. My proficiency in utilizing eTMF platforms has enabled me to streamline document management processes, facilitate audits and inspections, and ensure compliance with regulatory requirements and ALCOA-C guidelines.

• 

  State University Of New York College At Cortland

  Bachelor'S Degree