We are seeking an experienced Clinical Study Coordinator to join our growing team and work closely with the Principal Investigator on clinical trials. This role involves coordinating all aspects of study operations, including participant recruitment, data management, regulatory documentation, and study visit coordination.

QUALIFICATIONS

• Prior experience as a Clinical Research Coordinator required.
• Strong attention to detail and excellent interpersonal communication skills.
• Highly motivated, organized, and able to work independently.
• Proficiency in written and spoken English.
• Phlebotomy skills required (impeccable technique).
• Mental health research experience preferred.
• Experience as a rater for psychometric scales preferred.

• Collaborate with the Principal Investigator to ensure smooth study execution in compliance with protocols and regulations.
• Recruit and screen participants for clinical trials.
• Perform and document study procedures, including phlebotomy.
• Manage study data and maintain accurate regulatory and source documentation.
• Administer and score various psychological rating scales (training can be provided if needed).