Research Assistant

The Research Assistant performs a variety of administrative and clinical support tasks for clinical trials, assisting in the collection and management of patient data for enrolled or prospective study participants.

• Verify and correct research study information on source documents.
• Research queries and variances, providing feedback to site data collectors.
• Input research study data into Electronic Data Capture (EDC) systems, ensuring quality, accuracy, and completeness.
• Prepare and maintain study files and regulatory documentation.
• Compile, collate, and submit study information within established deadlines.
• Schedule subject visits and generate necessary reports and documents for research subjects.
• Input visit data into Clinical Trial Management System (CTMS) to track procedures against study budgets.
• Process required lab specimens, label vials, and complete requisitions for storage or shipment according to study protocols and regulations.
• Perform administrative tasks including reception, office organization, and supply management.

• Basic knowledge of clinical trials and study procedures.
• Familiarity with departmental, protocol, and study‑specific SOPs, consent forms, and schedules.
• Basic medical terminology knowledge.
• Proficiency in Microsoft Office applications (Word, Excel, Access, Outlook).
• Excellent interpersonal and communication skills.

• BS/BA in Life Sciences or equivalent education and/or relevant clinical experience (e.g., clinical research coordinator, nurse, medical assistant).