Clinical Research Coordinator - 245352 Job at Medix™, Hialeah, FL

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  • Medix™
  • Hialeah, FL

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,

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