Clinical Research Associate
| Company | St. Louis University |
|---|---|
| Location | St. Louis, MO, USA |
| Salary | $Not Provided – $Not Provided |
| Type | Full-Time |
| Degrees | Bachelor’s |
| Experience Level | Junior, Mid Level |
Requirements
- Knowledge of regulations and guidelines related to clinical research
- Working knowledge of clinical research terminology and multiple medical conditions
- Knowledge of GE Centricity, EPIC, Clinical Conductor CTMS and other University Electronic Data Systems
- Ability to efficiently operate computer software for Electronic Health Record and Practice Management Systems
- Strong interpersonal and customer service skills
- Excellent time management, organizational and multitasking skills
- Ability to maintain confidentiality
- Bachelor’s degree; supplemented with two (2) years of related work experience
Responsibilities
- Screens, recruits and enrolls patients into research studies in accordance with good clinical practice.
- Schedules and conducts research study visits.
- Provides technical and administrative expertise in the preparation and administration of investigational products.
- Records and documents study visits utilizing ALCOA+ principles.
- Data entry and query resolution.
- Maintains accurate and complete study documents.
- Liaise with Clinical Trials Office, SLU Institutional Review Board, SLU Radiation Safety Committee & SSM Research Compliance Office.
- Liaise with industry sponsors, CROs and vendors.
- Attends meetings, performs other duties as assigned.
- Performs other duties as assigned.
Preferred Qualifications
- CNMT Certification