Administrative Skills, Budget Management, Clinical Research, Clinical Trial, Communication Skills, Customer Support/Service, Data Collection, Data Entry, Detail Oriented, Expense Tracking, Federal Laws and Regulations, File Maintenance, Grant Administration/Management, Maintain Compliance, Medical Record System, Medical Terminology, Microsoft Excel, Microsoft Office, Microsoft PowerPoint, Microsoft Word, Obstetrics and Gynecology, Operations Research, Organizational Skills, Presentation/Verbal Skills, Purchasing/Procurement, Research Grants, Research Protocols, State Laws and Regulations, Team Player, Technical Support, Technical Writing, Women's Health, Writing Skills
Seeking motivated individual who enjoys multidisciplinary projects that involve collaboration and teamwork. The position holder will work closely with faculty in Obstetrics and Gynecology and in the Center for Inherited Oncogenesis to support clinical research studies. Experience in women's health will be an asset, but is not essential for candidates with other relevant experience.
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.
Responsibilities:
- 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.
Education:
- Can take 7 years of research coordination/related experience in lieu of Bachelors Degree.
U
UT Health San Antonio School of Dentistry