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).

• Bachelors degree in sciences or related field.
• 2 years of clinical research

 

Compensation Statement

 

 

• 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.