Clinical Research Coordinator
| Company | Hospital Sisters Health System |
|---|---|
| Location | O’Fallon, IL, USA |
| Salary | $28.14 – $42.21 |
| Type | Full-Time |
| Degrees | Bachelor’s |
| Experience Level | Junior, Mid Level |
Requirements
- Bachelor’s degree in a nursing, science or healthcare related field is required.
- 2 years healthcare or clinical research experience is required.
- Healthcare-related license if applicable.
- Human Subject Protection and Good Clinical Practices Training through the Collaborative Institutional Training Initiative (CITI) required within 30 days of hire.
Responsibilities
- Management of multiple clinical research trials.
- Selection and analysis of potential patients for study participation.
- Obtaining informed consent.
- Documentation of all study required case report forms.
- Identifying potential adverse events and reporting them to FDA/IRB/Study Sponsor as applicable.
- Ensuring that site/principal investigator is compliant with approved protocols.
- Acting as a liaison between patients, their families and other healthcare professionals during their participation in a research trial.
Preferred Qualifications
- Master’s degree in healthcare, research, business or related discipline is preferred.
- 2 years of experience in research is preferred.
- Clinical research professional certification (i.e., Certified Clinical Research Coordinator (CCRC) is preferred within 3 years of employment).