OPS - Clinical Research Coordinator
University of Florida - Chemical Engineering Masters Program · Gainesville, FL · Today
Research$21.1/hrPart-time
Job Description
Career Activities include the following:
- screen, recruit and consent eligible participants
- work with clinical team to collect and enter patient data
- perform chart review
- attend relevant trainings and meetings
- coordinate communication for the study team
Additional activities include:
- managing data and performing quality assurance checks for the Informed Consent and other relevant study documents
- working with clinical research study team to prepare for study visits
- preparing study questionnaires, scheduling patient visits and coordinating communication
- labeling and processing clinical samples as needed
- managing data queries
- assisting with projects to support related clinical initiatives
- maintaining accurate records within OnCore
- running reports as requested
- maintaining up-to-date study records
Qualifications
Required Qualifications:
- Associate’s degree or an allied health professional degree in an appropriate area and one year of relevant experience
- or an equivalent combination of education and experience
Preferred Qualifications:
- Experience Working In a Clinical Setting
- Preferred Experience working within UF’s clinical research system preferred
- Multi-media capabilities strongly preferred
- Proficiency with Microsoft Office such as Word, PowerPoint and Excel
Benefits
Not specified
Pay
$21.10 hourly
Schedule
Not specified
Skills
Not specified
Benefits
Not specified
Contact Information
To apply, you must upload your cover letter and resume. Applications must be submitted by 11:55 p.m. (ET) of the posting end date.
Health Assessment Required: Yes