Clinical Research Coordinator, Part-Time-Psychiatry

Benefits

Responsibilities

• •The Clinical Research Coordinator, Part-time performs all the regular duties of a Clinical Research Coordinator, but due to abbreviated hours doesn't qualify for exemption
• •This is an hourly position which is eligible for overtime only intended to be used for part-time employees
• •The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information
• •Assists in preparing grant applications and documents (for e.g., Institutional Review Board, Grants and Contracts Office)
• •Collects and records study data
• •Inputs all information into database
• •Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements
• •Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screening participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires
• •Assists in preparing grant applications, IRB/GCO for submission and filings
• •Maintains source documents and subject files in accordance with hospital procedures
• •Ensures accurate and complete compilation of subject data through chart reviews
• •Secures, delivers and ships clinical specimens as required by the protocol
• •Prepares for monitoring visits
• •Performs other related duties
• •11 more items(s)