Clinical Research Coordinator (Psychiatry/CNS)

Clinical Research Coordinator (Psychiatry/CNS)

Location: Boynton Beach, FL
Job Type: Full-Time, Permanent
Schedule: Monday-Friday | 8:00 AM - 4:30 PM
Setting: Outpatient Clinical Research

Position Overview

We are seeking an experienced and motivated Clinical Research Coordinator (CRC) to join a growing outpatient clinical research team. This opportunity is ideal for a clinically experienced professional with prior research experience who is passionate about patient care, organization, and advancing medicine through clinical trials.

The ideal candidate will be bilingual in English and Spanish, possess strong clinical skills, and thrive in a fast-paced research environment. This role offers the opportunity to work closely with physicians, sponsors, and study participants while contributing to innovative Psychiatry/CNS research studies.

Responsibilities
• Coordinate and manage clinical research studies within Psychiatry/CNS therapeutic areas.
• Conduct patient visits and perform study-related procedures, including vital signs, ECGs, phlebotomy, lab processing, and specimen handling.
• Recruit, screen, consent, and enroll study participants.
• Administer and/or assist with protocol-required psychiatric rating scales and clinical assessments.

Qualifications

Required
• Prior clinical research experience.
• Bilingual in English and Spanish.
• Experience administering Psychiatry/CNS clinical rating scales and assessments is required, including experience with some or all of the following:
• MADRS (Montgomery-Åsberg Depression Rating Scale)
• CGI-S (Clinical Global Impression - Severity Scale)
• CHRT-C (Concise Health Risk Tracking Scale - Clinician)
• SCID-5 (Structured Clinical Interview for DSM-5 Disorders)
• ATRQ (Antidepressant Treatment Response Questionnaire)
• MGH ATRQ (Massachusetts General Hospital Antidepressant Treatment Response Questionnaire)
• BTRQ (Bipolar Disorder Treatment Response Questionnaire)
• Strong knowledge of medical terminology and clinical laboratory procedures.
• Understanding of GCP guidelines and FDA regulations.
• Excellent organizational, communication, and multitasking skills.

Preferred
• MA, LPN, or RN certification/licensure.
• Experience with EMR systems.
• Experience with EDC systems, eSource, and clinical research documentation.
• Prior experience coordinating Psychiatry, CNS, Depression, Bipolar Disorder, or Mood Disorder clinical trials.

Benefits
• Medical Insurance
• Dental Insurance
• Vision Insurance
• 401(k) Retirement Plan
• Career Growth Opportunities
• Supportive and Collaborative Team Environment
• Opportunity to Work on Cutting-Edge Clinical Trials

If you're interested or want more details, feel free to call me at(469) 272-6319 or email me at [email protected]. Looking forward to connecting!

#INDPRO