What are the responsibilities and job description for the Clinical Research Coordinator/Registered Nurse (RN) position at MCR Health, Inc?
Brief Description
Why MCR Health?
A career at MCR Health offers exciting opportunities with one of the largest Healthcare companies in the areas we serve. Now, more than ever, we are looking for exceptional people to support our passion to provide "Exceptional Care to Everyone, Every Time" and to support our Mission to serve everyone. Whether you provide direct patient care or in other areas of our Company, you can find a home here. We invite you to be part of our community, where you can grow your career and serve with your heart.
In our time of Company growth, we are seeking a Clinical Research Coordinator
Work Location: Bradenton, FL
As Part Of This Role, You Will
What you need to bring to this role:
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.
Why MCR Health?
A career at MCR Health offers exciting opportunities with one of the largest Healthcare companies in the areas we serve. Now, more than ever, we are looking for exceptional people to support our passion to provide "Exceptional Care to Everyone, Every Time" and to support our Mission to serve everyone. Whether you provide direct patient care or in other areas of our Company, you can find a home here. We invite you to be part of our community, where you can grow your career and serve with your heart.
In our time of Company growth, 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.
What you need to bring to this role:
- 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.
- 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 Products-Word, Excel, Outlook, PowerPoint proficiency preferred
- Minimum 3 years of clinical research experience required CCRC or equivalent certification preferred
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.