Clinical Research Coordinator/Registered Nurse
About The Position
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 work 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/Register Nurse Work Location: Bradenton, FL As part of this role, you will: Assist in protocol review and study start-up activities Prepare regulatory documents for IRB/EC submission and maintain approvals Recruit, screen, and enroll participants according to inclusion/exclusion criteria Obtain informed consent and ensure the participant's safety and confidentiality Collect and record study data accurately in case report forms (CRFs) and electronic systems Maintain source documents and ensure data integrity Adhere to GCP, FDA, and institutional guidelines Responsible for providing vital signs, interviewing the patient/family, and charting Collaborates with healthcare providers in assessing, planning, implementing, and evaluating the needs of patients and peers Knowledgeable and assists Providers as requested with exams, procedures, removal of sutures, etc. Completes medication and DME authorizations for patients in a timely manner Knowledgeable in walk-in triage and interventions regarding patients' age under the leadership of the Clinical Nurse Leader Knowledgeable regarding all medical forms (PE, work excuses, proof of pregnancy, etc.) Knowledgeable regarding patient-specific reports and logs
Responsibilities
- Assist in protocol review and study start-up activities
- Prepare regulatory documents for IRB/EC submission and maintain approvals
- Recruit, screen, and enroll participants according to inclusion/exclusion criteria
- Obtain informed consent and ensure the participant's safety and confidentiality
- Collect and record study data accurately in case report forms (CRFs) and electronic systems
- Maintain source documents and ensure data integrity
- Adhere to GCP, FDA, and institutional guidelines
- Responsible for providing vital signs, interviewing the patient/family, and charting
- Collaborates with healthcare providers in assessing, planning, implementing, and evaluating the needs of patients and peers
- Knowledgeable and assists Providers as requested with exams, procedures, removal of sutures, etc.
- Completes medication and DME authorizations for patients in a timely manner
- Knowledgeable in walk-in triage and interventions regarding patients' age under the leadership of the Clinical Nurse Leader
- Knowledgeable regarding all medical forms (PE, work excuses, proof of pregnancy, etc.)
- Knowledgeable regarding patient-specific reports and logs
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What This Job Offers
Career Level
Entry Level
Education Level
No Education Listed
Number of Employees
501-1,000 employees
