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Clinical Research Coordinator (RN)

  • Clinical Research Coordinator (RN) job type Posted on: Oct 31, 2026
  • Clinical Research Coordinator (RN) experience level NRx Pharmaceuticals, Inc.
  • Clinical Research Coordinator (RN) employment type West Palm Beach, Florida
  • Clinical Research Coordinator (RN) salary Salary: $42 per hour
  • Clinical Research Coordinator (RN) employment type Onsite
  • Clinical Research Coordinator (RN) salary Part-time

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Job Title :

Clinical Research Coordinator (RN)

Job Type :

Part-Time

Job Location :

West Palm Beach Florida United States

Remote :

No

Jobcon Logo Job Description :

This position sits with NRx Defense Systems and is performed on-site at HOPE Therapeutics in West Palm Beach, Florida. HOPE Therapeutics is a clinical subsidiary of NRx Pharmaceuticals (Nasdaq: NRXP) and operates an interventional psychiatry clinical network across Florida. We're launching a pivotal Phase III depression trial and hiring an experienced RN to lead study operations at this site. The role starts part-time and is planned to grow to full-time as enrollment ramps up.The roleYou'll be the face and voice of the site: the main contact for patients, sponsors, CROs and monitors. You'll work under the direct oversight of the Principal Investigator. She will delegate clinical tasks to you, so she needs to be able to rely on your clinical judgment and your documentation. Success means three things: patients are enrolled on target, participants stay in the study and are managed safely, and the site is ready for an FDA inspection at all times.What you'll doReview medical records to find, pre-screen and enroll eligible patients against sponsor targetsAssess eligibility, obtain informed consent and manage participants through every study visitCarry out clinical tasks the PI delegates to you, including phlebotomy, specimen processing and shipping to labs, and study procedures as trainedKeep patients in the study with reminder calls, visit-prep instructions and ongoing follow-upIdentify and report AEs and SAEs within protocol timelinesKeep EDC data, TMF/ISF and source documents current and ready for inspectionHelp the PI keep the site compliant with ICH-GCP, including the delegation log, IRB submissions, deviations and IP accountabilityLead the site through monitoring visits, audits and FDA inspections, including CAPA responsesWhat you bringActive RN license eligible to practice in Florida (Florida license or eNLC multistate)Experience as Lead or Primary Study Coordinator on pharma-sponsored trials5+ years of hands-on patient evaluation and managementExperience caring for mental health patientsPhlebotomy skills and experience handling specimensWorking knowledge of ICH-GCP, 21 CFR, EDC and TMF systemsStrongly preferredTrial experience in MDD, TRD, suicidal ideation and behavior, or bipolar depressionExperience with MADRS, HAM-D or C-SSRS, or rater certificationTMS, ketamine or esketamine experience (TMS training is a plus)Phase III or registrational trial experience, including FDA inspectionsCCRC or ACRP-CP certificationCompensation & benefits$42–52/hour, depending on experience and certification. Medical, dental, vision, 401(k), PTO, and support for licensure and research certification.NRx Defense Systems, HOPE Therapeutics and NRx Pharmaceuticals are equal opportunity employers.

Jobcon Logo Position Details

Posted:

Oct 31, 2026

Reference Number:

10440_4471494526

Employment:

Part-time

Salary:

$42 per hour

City:

West Palm Beach

Job Origin:

APPCAST_CPC

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This position sits with NRx Defense Systems and is performed on-site at HOPE Therapeutics in West Palm Beach, Florida. HOPE Therapeutics is a clinical subsidiary of NRx Pharmaceuticals (Nasdaq: NRXP) and operates an interventional psychiatry clinical network across Florida. We're launching a pivotal Phase III depression trial and hiring an experienced RN to lead study operations at this site. The role starts part-time and is planned to grow to full-time as enrollment ramps up.The roleYou'll be the face and voice of the site: the main contact for patients, sponsors, CROs and monitors. You'll work under the direct oversight of the Principal Investigator. She will delegate clinical tasks to you, so she needs to be able to rely on your clinical judgment and your documentation. Success means three things: patients are enrolled on target, participants stay in the study and are managed safely, and the site is ready for an FDA inspection at all times.What you'll doReview medical records to find, pre-screen and enroll eligible patients against sponsor targetsAssess eligibility, obtain informed consent and manage participants through every study visitCarry out clinical tasks the PI delegates to you, including phlebotomy, specimen processing and shipping to labs, and study procedures as trainedKeep patients in the study with reminder calls, visit-prep instructions and ongoing follow-upIdentify and report AEs and SAEs within protocol timelinesKeep EDC data, TMF/ISF and source documents current and ready for inspectionHelp the PI keep the site compliant with ICH-GCP, including the delegation log, IRB submissions, deviations and IP accountabilityLead the site through monitoring visits, audits and FDA inspections, including CAPA responsesWhat you bringActive RN license eligible to practice in Florida (Florida license or eNLC multistate)Experience as Lead or Primary Study Coordinator on pharma-sponsored trials5+ years of hands-on patient evaluation and managementExperience caring for mental health patientsPhlebotomy skills and experience handling specimensWorking knowledge of ICH-GCP, 21 CFR, EDC and TMF systemsStrongly preferredTrial experience in MDD, TRD, suicidal ideation and behavior, or bipolar depressionExperience with MADRS, HAM-D or C-SSRS, or rater certificationTMS, ketamine or esketamine experience (TMS training is a plus)Phase III or registrational trial experience, including FDA inspectionsCCRC or ACRP-CP certificationCompensation & benefits$42–52/hour, depending on experience and certification. Medical, dental, vision, 401(k), PTO, and support for licensure and research certification.NRx Defense Systems, HOPE Therapeutics and NRx Pharmaceuticals are equal opportunity employers.

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