Upvote
Downvote
Clinical Research Coordinator I, II, And III. IMPACTS
Share Job
- Suggest Revision
- Summary The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials in cardiovascular and chronic kidney diseases.
- The Clinical Research Coordinator assists the investigator team to develop study protocols and manuals of procedures.
- The Clinical Research Coordinator screens, enrolls and follows study participants, conducts data collection and entry, and performs noninvasive cardiovascular tests according to study protocols.
- The Clinical Research Coordinator is also responsible for keeping all data and source documentations, adverse event reporting, and IRB regulatory files.
- Required Knowledge, Skills, and Abilities •Must be able to interact well with patients and the general public•Ability to acquire and maintain all required CITI training certificates•Ability to acquire and maintain credentialing at all required institutions Required Education and/or Experience The education required for each level is listed below:Clinical Research Coordinator I (Pay Grade 23)
Active Job
Updated TodaySimilar Job
Relevance
Active