The Research Coordinator performs a vital role for the Clinical Research Office (CRO) by coordinating various components of multiple clinical research studies at any time. This position reports to the CRO Associate Directors.
Primary responsibilities of the Research Coordinator include, but are not limited to:
- Undertake coordinating tasks of clinical research studies. Resolve queries in a timely manner. Generate accurate reports.
- Guide day-to-day operations of assigned studies, assuring adherence to protocol.
- Generate IRB approved materials for distribution to study subjects to promote project enrollment and retention of enrolled subjects.
- Oversee implementation of research studies, generation of qualitative and quantitative data and data collection forms and surveys.
- Manage the day-to-day operations of the assigned project including development and implementation of research procedures and systems.
- Assist Principal Investigator with administration of clinical trial protocols, including obtaining informed consents and screening subjects, maintaining research records and research subject records, managing correspondence, researching medical records, recording data, and attending training sessions.
Minimum Qualifications
- Bachelor’s degree and 2 years of clinical research-related experience, or an equivalent combination of education and experience.
- Applicants must be familiar with clinical research procedures and methodology.
Preferred Qualifications
- Nursing degree preferred but not required.
Salary Range
$55,000 – $90,000
