Under general supervision, responsible for providing specialized administrative support in a laboratory and/or clinical research environment.

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• Knowledge in grant administration, research coordination, data collection, and/or facilitating the patient experience in research projects.
• Working knowledge with electronic health record systems and familiarity with medical terminology.
• Strong written and verbal communication skills to include the ability to generate high quality, technical writing and written/oral presentations.
• Proficient in using Microsoft Office (Word, Excel, PowerPoint) and databases.
• Detail oriented with meticulous planning, organizational and customer service skills.

EDUCATION:

Bachelor's Degree degree in a related field is required.

PREFERRED:

Bilingual (English/Spanish)

Clinical Research Certification

Phlebotomy experience

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• Coordinates multiple research protocols and grant submissions. Assists with monitoring budgets, spending, purchasing and participant payments.
• Creates, completes and tracks forms and reports for study sponsors.
• Schedules on-site visits or meetings and prepares agendas as indicated.
• Provides routine technical/administrative assistance in performing assigned and delegated tasks in support of research projects to ensure continuous clinical research operations.
• Maintains research subject files for each clinical study and enters all subject data into research database.
• Monitors ongoing activities on various research studies to ensure compliance with local, state & federal regulations.
• Performs all other duties as assigned.