Clinical Research Coord I
Tanner Clinic
- Layton, UT
- Permanent
- Full-time
- Coordination and management of the clinical trial, generating source documents on Microsoft Word, time management, visit coordination, product dispensing and accountability, managing monitoring visits, and communication with sponsor and authorities
- Data collection and management, obtaining medical histories and vital signs, performing phlebotomy, lab processing and shipping, recording and management of AEs, completing CRFs, filing and archiving, and resolving queries
- Other duties as assigned
- Background in a medical field and/or completed college level human body related courses.
- Certifications and/or licenses are preferred but not required: CCRC, CNA, CMA, LPN
- Previous clinical research experience is preferred but not required.
- Excellent written and verbal communications skills
- Highly motivated, organized and strong attention to detail.
- Knowledge of administrative and clerical procedures and systems such as word processing, managing files and records, designing forms, and other office procedures and terminology.
- Communicating effectively in writing as appropriate for the needs of the audience.
- The ability to apply general rules to specific problems to produce answers that make sense.