Clinical Research Coordinator I-Pathology, Molecular and Cell Based Medicine

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Prepares tissue samples for analyses. 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, including sample preparation using standard immunological techniques; maintains data/results of all experiments.

• Bachelors or Masters degree in Science or closely related field.
• No experience required. One year of research experience preferred.

Preferred

• 1-2 years of previous clinical research experience
• Excellent written and oral communication skills
• Exceptional attention to detail