Clinical Research Coordinator/Registered Nurse (RN)
MCR Health, Inc, Bradenton, FL, United States
We are seeking a Clinical Research Coordinator.
Work Location: Bradenton, FL.
As Part Of This Role, You Will
Coordinate daily operational activities for assigned clinical trials.
Support participant recruitment coordination, consent logistics, and visit scheduling.
Maintain communication with Sponsors and CROs.
Transcribe and verify study data from source documentation into electronic data capture (eCRF) systems.
Coordinate data query resolution and support data integrity processes.
Maintain study files and assist with site-level regulatory documentation.
Support preparation for monitoring visits and administrative aspects of audits.
Assist with study close‑out activities and documentation organization.
Requirements
Bachelor’s degree in life sciences or related field.
Experience in clinical research coordination preferred.
Knowledge of Good Clinical Practice (GCP) principles.
Strong organizational and communication skills.
Current BLS Certification through the American Heart Association, American Red Cross, or American Safety and Health Institute is required.
Microsoft Office – Word, Excel, Outlook, PowerPoint proficiency preferred.
Minimum 3 years of clinical research experience required; CCRC or equivalent certification preferred.
Summary
The Clinical Research Coordinator (CRC) is a non‑clinical research role responsible for coordinating operational aspects of clinical trials and supporting data management activities. The CRC supports study execution under the supervision of the Principal Investigator and clinical team, ensuring adherence to protocol requirements and operational workflows.
MCR Health is a drug‑free workplace. All job applicants selected for employment must submit to a pre‑employment drug test and background check.
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Work Location: Bradenton, FL.
As Part Of This Role, You Will
Coordinate daily operational activities for assigned clinical trials.
Support participant recruitment coordination, consent logistics, and visit scheduling.
Maintain communication with Sponsors and CROs.
Transcribe and verify study data from source documentation into electronic data capture (eCRF) systems.
Coordinate data query resolution and support data integrity processes.
Maintain study files and assist with site-level regulatory documentation.
Support preparation for monitoring visits and administrative aspects of audits.
Assist with study close‑out activities and documentation organization.
Requirements
Bachelor’s degree in life sciences or related field.
Experience in clinical research coordination preferred.
Knowledge of Good Clinical Practice (GCP) principles.
Strong organizational and communication skills.
Current BLS Certification through the American Heart Association, American Red Cross, or American Safety and Health Institute is required.
Microsoft Office – Word, Excel, Outlook, PowerPoint proficiency preferred.
Minimum 3 years of clinical research experience required; CCRC or equivalent certification preferred.
Summary
The Clinical Research Coordinator (CRC) is a non‑clinical research role responsible for coordinating operational aspects of clinical trials and supporting data management activities. The CRC supports study execution under the supervision of the Principal Investigator and clinical team, ensuring adherence to protocol requirements and operational workflows.
MCR Health is a drug‑free workplace. All job applicants selected for employment must submit to a pre‑employment drug test and background check.
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