Clinical Research Coordinator Position

6 days ago


Staten Island, New York, United States Medix™ Full time

Clinical Research Coordinator Opportunity

Medix is seeking a skilled Research Professional to join our team in Staten Island, NY. As a Clinical Research Coordinator, you will play a crucial role in the success of our clinical trials.

Key Responsibilities:

  • Coordinate all aspects of the study, including recruitment, consent, screening, scheduling, and tracking.
  • Collect and enter data into study case report forms and/or electronic data capture system, and respond to queries in a timely manner.
  • Submit study-related documents, study protocols, and study protocol amendments to the IRB per policy and procedure.
  • Ensure procedural documentation is accurate, complete, and in compliance with institutional, local, state, and federal guidelines and regulations related to clinical research.
  • Collect, process, and ship potentially biohazardous specimens.
  • Administer structured tests and questionnaires according to research study protocols, and utilize study-related technology and equipment as part of assessment procedures.
  • Provide ongoing study status updates, respond to questions, and create summary reports for distribution to PI, Administrator, Office of Research Affairs, Sponsor, and Compliance.
  • Organize and participate in auditing and monitoring visits.

Requirements:

  • High School Diploma or equivalent; College degree preferred.
  • Two to four years of experience or certification as a Clinical Research Coordinator.
  • Psych experience preferred.

Details:

Location: Staten Island, NY.

Pay: $24/hr-$30/hr (dependent on background and years of experience).

Hours: Monday - Friday; Normal Business Hours; Onsite 5 Days a Week.

Duration: ~6 month (1,040 Hours) contracted probationary period into direct hire/permanent position.



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