Site Coordinator, Data Entry

Responsibilities Perform accurate and timely data entry into study systems in line with protocols and SOPs Support query resolution and ensure data quality and completeness Assist with Serious Adverse Event reporting activities Maintain and update Investigator Site Files and study documentation Support Ethics Committee submissions and regulatory documentation Assist with study drug accountability logs and tracking Support monitoring visits, audits, and inspections when required Manage patient expense documentation and administrative follow up Provide general administrative support to the study team as needed Requirements Bachelor’s degree in Life Sciences or similar field, or equivalent relevant experience Previous experience with data entry, administrative support, or clinical research activities Strong attention to detail and ability to manage structured data accurately Good organizational skills with the ability to prioritize and manage multiple tasks Good communication skills in English, both written and verbal Ability to work independently in a flexible, part time setup Willingness to travel on site in Maryland for approximately 20 hours per month #J-18808-Ljbffr Jobtailor