Clinical Research Coordinator I- Mindich Child Health & Dev. Institute

Description

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).

Responsibilities

• 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.

Qualifications

Required Experience :

IC

Key Skills

EMR Systems,Employee Relations,Typing,Patient Care,Clerical Experience,HIPAA,Computer Skills,EMT Experience,Medical Terminology,Transcription,Epic,Phone Etiquette

Employment Type : Full-Time

Experience : years

Vacancy : 1