Clinical Research Coordinator (HS)- Neurology
Core
Coordinate and perform daily clinical research activities for stroke and neurocritical care protocols, including patient recruitment, consent, data collection, and regulatory compliance.
Role type
Clinical Research Coordinator (IC)
Builds
Clinical research protocols and data for stroke and neurocritical care studies
Domain
Healthcare / Clinical Research / Neurology
Required skills
Patient recruitment and enrollment, Informed consent administration, Clinical data collection and coding, Adverse event monitoring, Protocol compliance, Biological sample processing, Standardized scoring of diagnostic/behavioral testing, Report generation
Preferred skills
Stroke and cerebrovascular disease knowledge, Inpatient unit experience, Fast-paced environment experience, Medical terminology knowledge, Clinical research certification, Microsoft Office proficiency
Technologies
Microsoft Office applications
Responsibilities
Recruit, interview, and enroll patients; Obtain informed consent; Coordinate patient appointments and diagnostic testing; Collect, process, and evaluate biological samples; Administer and score diagnostic/behavioral tests; Monitor patients for adverse reactions; Document and report unfavorable responses; Evaluate patient compliance; Collect and analyze clinical research data; Ensure compliance with IRB, FDA, and sponsor regulations; Participate in developing new research protocols.
Seniority
Individual contributor, specialized