JOB DESCRIPTION
The Clinical Research Coordinator assists the daily activities of the clinical research studies, obtains informed consents; collects, maintains and organizes study information. Assists in preparing grant applications and documents (for e.g. Institutional Review Board, Grants and Contracts Office).
Duties and Responsibilities:
1.	Collects and records study data. Inputs all information into database.
2.	Obtains informed consent under minimal supervision of the investigator(s) and educates participants regarding study requirements.
3.	Assists in the activities related to clinical research studies including but not limited to: answering phone calls, screen participants for eligibility, registering subjects with sponsoring agency, administering lifestyle questionnaires.
4.	Assists in preparing grant applications, IRB/GCO for submission and filings. 
5.	Maintains source documents and subject files in accordance with hospital procedures. Ensures accurate and complete compilation of subject data through charts reviews. 
6.	Secures, delivers and ships clinical specimens as required by the protocol. 
7.	Prepares for monitoring visits.
8.	Performs other related duties.
JOB QUALIFICATIONS
Education:
Bachelor’s in Science or closely related field
Skills: 
Excellent written and oral communication skills, team player, 2 year commitment 
Exception attention to detail and accuracy

If interested please direct your cover letter and CV to [log in to unmask]