Emily Malott Email & Phone Number

Raleigh, Nc, Us

-Screen potential study participants according to protocol inclusion and exclusion criteria by asking study-specific questions.-Review, enter, and edit patient information into clinical trial management software to maintain accurate records.-Schedule patient appointments, ensuring all entries in site schedulers are precise and up to date.-Understand and articulate the purpose and inclusion/exclusion criteria for each clinical trial protocol.-Respond to all leads within a 24-hour timeframe to facilitate timely engagement.-Identify suitable study opportunities for interested volunteers, leveraging knowledge of clinical trials and local options.-Develop problem-solving strategies and contingency plans to optimize enrollment rates.-Communicate the importance of research participation effectively to volunteers, fostering understanding and interest.-Provide an exceptional patient experience by building positive rapport and maintaining consistent follow-up.-Strive to meet personal and team targets, contributing to overall recruitment goals.-Adhere to strict confidentiality protocols in all communications, including electronic, written, and verbal forms.-Ensure high-quality, accurate work by properly organizing and filing all administrative documentation.-Self-motivated and capable of organizing workload to ensure effective delivery of delegated tasks and projects.-Demonstrate business curiosity that aligns with ICON values, contributing to a collaborative work environment.

Post, Clinical Research

Bachelor Of Science - Bs, Zoology/Animal Biology