CLINICAL STUDY COORDINATOR- 6-9 month contract
SUMMARY:
Clinical Research Coordinator needed to support critical care clinical research.
DUTIES & RESPONSIBILITIES:
* Clinical document review
* Document redactions
* EDC document uploads and related data-entry
* Other duties, as required
QUALIFICATIONS & REQUIREMENTS:
* 3 years of relevant experience as a clinical study coordinator
* Proficient in EPIC EHR software
* Good quality control, and written, verbal and interpersonal communication skills and computer and EDC proficiency
* Critical care research experience and perioperative experience are preferred
LOCATION:
Work will be performed onsite in the greater Boston, Massachusetts area
