Job Description
Job Title: Clinical Research Coordinator – Psychiatry
Location: Miami Lakes (On-site)
Employment Type: Full-Time
Schedule: Monday–Friday, standard business hours; some weekend availability may be required based on study needs
Pay: Dependent on experience, range is $60,000-$80,000 annual
Job Description:
We are seeking a Clinical Research Coordinator (CRC) with a minimum of 4 years of experience to join a leading multi-site research facility specializing in psychiatric and central nervous system (CNS) clinical trials. The CRC will play a key role in managing the day-to-day execution of outpatient clinical trials and must be comfortable working with complex patient populations in a high-volume, fast-paced environment.
Key Responsibilities:
- Coordinate and manage assigned clinical trials in accordance with study protocols, GCP, ICH guidelines, and site SOPs
- Screen, recruit, and consent eligible study participants, including thorough explanation of study procedures
- Conduct study visits and assessments, including administering psychiatric rating scales (training provided if needed)
- Collect and record vital signs, ECGs, and assist with specimen collection as needed
- Maintain accurate, timely, and complete source documentation and case report forms
- Ensure timely data entry and resolution of queries within EDC platforms
- Prepare for and participate in sponsor and monitor visits, audits, and inspections
- Maintain regulatory documentation and assist with IRB submissions, updates, and essential document tracking
- Work collaboratively with investigators, research staff, and clinical operations team
- Handle investigational product (IP) accountability in compliance with study protocols
Qualifications:
- Minimum of 4 years of experience as a Clinical Research Coordinator
- Experience in psychiatric or CNS clinical trials required
- Strong knowledge of clinical trial regulations, GCP, and protocol adherence
- Comfort working with vulnerable or high-acuity patient populations (e.g., depression, schizophrenia, bipolar disorder)
- Experience with electronic data capture (EDC) systems such as Medidata, Veeva, or similar
- Ability to manage multiple studies concurrently in a dynamic environment
- Excellent written and verbal communication skills
- Phlebotomy and lab processing experience is a plus
- Bilingual (English/Spanish) preferred but not required
Job Tags
Full time, Weekend work, Monday to Friday,