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Clinical Study Coordinator
2 months ago
This is a full-time workload for the first month, and should average 20 hours per week, up to 80 hours per month
CLINICAL STUDY COORDINATOR
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
- Perioperative surgery experience and experience with Critical Care Research involving data collected in ICU settings are big pluses.
LOCATION:
Work will be performed onsite in the greater Boston, Massachusetts area