Clinical Research Coordinator II-Neurosurgery
Full-time
Internal Medicine
Description
Under minimal supervision coordinates the clinical assessments of the study subjects; analyzes and assists in interpreting moderately complex clinical research data. Prepares grant applications and documents and assists in protocol submissions (for e.g. Institutional Review Board Grants and Contracts Office).
Responsibilities- Analyzes moderately complex clinical research data; Assists in interpreting clinical research data.
- Coordinates the clinical assessments of the study subjects including but not limited to screening and evaluation of the study subjects.
- Prepares and ensures grant applications IRB/GCO documents are submitted.
- Ensures accurate and complete compilation of subject data through chart reviews.
- Assists the Principal Investigator and regulatory staff in the preparation of new protocol submissions protocol amendments and renewals of ongoing clinical trials.
- Obtains informed consent under supervision of the Principal Investigator Clinical Research Manager or Senior Clinical Research Coordinator for studies enrolling vulnerable subjects and for studies involving genetic tests.
- Independently obtains informed consent for other clinical studies.
- Mentors Clinical Research Coordinators in training.
- Performs other related duties.
- Bachelors degree in sciences or related field.
- 2 years of clinical research
Compensation Statement
Required Experience:
IC
Vacancy posted 1 day ago
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