Clinical Study Assistant
Clinical Study Assistant
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Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Supports administrative operations and coordination of human subjects research studies.
Responsibilities
1. Maintain supply inventory including ordering supplemental test articles and returning unused test articles to sponsor. 2. Prepares and maintains regulatory documents. 3. Enters demographic information into a database. 4. Determines visit windows from protocol schedules subject visits and sends visit reminders. 5. Organizes and prepares area for study related equipment and supplies. 6. Schedules and coordinates prestudy and monitor site visits. 7. Transmits Case Report Form data by fax express mail or other means dictated by sponsor. 8. Ensures study visits and procedures do not conflict with existing schedules. This job description is not designed to contain or be interpreted as a comprehensive inventory of all duties responsibilities and qualifications required of employees assigned to the job. Work Environment and Level of Frequency typically required Nearly Continuously: Office environment. Seldom: Infectious disease exposure to animals oils there is air or skin exposure to oils or other cutting fluids Physical Requirements and Level of Frequency that may be required Nearly Continuously: Sitting hearing listening talking. Often: Repetitive hand motion (such as typing) walking. Seldom: Bending reaching overhead.
Minimum Qualifications
Associates degree or equivalency (one year of education can be substituted for two years of related work experience). Completion of HIPAA Privacy & Security training may be required within two to five days of hire. Demonstrated human relations and effective communication skills also required. Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description.
Employment Type
Full Time
