Medix
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
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