Under general supervision, responsible for providing specialized administrative support in a laboratory and/or clinical research environment.
- Provides routine technical/administrative assistance in performing assigned and delegated tasks in support of research projects to ensure continuous clinical research operations.
- Knowledge in grant administration, research coordination, data collection, and/or facilitating the patient experience in research projects (reviewing patient charts for eligibility, scheduling, consenting etc.).
- Coordinates 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.
- 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.
- Working knowledge with electronic health record systems and familiarity.
- 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.
Required Skills
Three (3) years of progressive experience in grant administration, research coordination, data collection, and/or facilitating the patient experience in research projects is required.
