Clinical Research Coordinator I, Psychiatry

About the Role

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.

Key Responsibilities

• Collects and records study data. Inputs all information into database.
• Obtains informed consent under minimal supervision and educates participants regarding study requirements.
• Assists in clinical research study activities including: answering phone calls, screening participants for eligibility, registering subjects, 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.

Requirements & Tech Stack

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