Circulating RN, PRN
CenExel
Summary
With moderate oversight, the Clinical Research RN I is responsible for overseeing the implementation of daily clinical study activities. Serving as a liaison between the investigative site and the Sponsor. Responsible for accurately and ethically documenting all information obtained throughout the clinical research process.
Job description
Job Summary
With moderate oversight, the Clinical Research RN I is responsible for overseeing the implementation of daily clinical study activities. Serving as a liaison between the investigative site and the Sponsor. Responsible for accurately and ethically documenting all information obtained throughout the clinical research process.
Essential Responsibilities and Duties
- Prepares the OR and verifies that equipment and supplies are available
- Confirms the patient, procedure, consent, and surgical site
- Helps position and prepare the patient for surgery
- Monitors patient safety throughout the procedure
- Coordinates with the surgeon, Surgical Tech, and anesthesia team
- Documents the surgery and nursing care
- Obtains additional supplies or equipment as needed
- Helps perform sponge, needle, and instrument counts
- Assists with transferring the patient to the PACU after surgery
- Maintains adequate inventory of all data and supplies
- Regularly attends training meetings, staff meetings, initiation meetings, study start-up meetings, and other meetings as assigned
- Observes, documents, reports, and follows up on adverse events and serious adverse events
- Conducts the informed consent process, per CenExel Standard Operating Procedures
- Follows up appropriately on all laboratory results
- Maintains safety standards when performing job responsibilities
- Maintains study logs and site relations
- Ensures proper collection, processing, and shipment (if applicable) of laboratory specimens
- Assists with quality assurance activities and completes queries, as applicable
- Obtains Principal Investigator signatures on necessary documents
- Oversees or coordinates the administration of investigational medication and follows subjects throughout the study stay, per protocol
- Ensures accountability and adequate supply for study and clinical drugs
- Supports and ensures strictest adherence to best practices, FDA Code of Federal Regulations, ICH, GCP, CenExel standard operating procedures, site working Practices, protocol, and company guidelines and policies
- Assumes other duties and responsibilities as assigned
Education/Experience/Skills
- Must be a Registered Nurse with a current license in Florida, and not have any disciplinary action on the license
- Must be BLS or ACLS certified or able to obtain
- 0-1 year of experience is required
- Must be IV certified, depending on site
- Must be capable of performing all clinical tasks relevant to licensure and/or training
- Must be able to clearly communicate verbally with patients
- Must have good interpersonal skills, demonstrated through interactions with patients, staff, Sponsor representatives, etc
- Must be self-motivated and able to perform tasks independently
- Ability to react calmly and effectively in emergency situations
- Must reflect the professional image of the company, upholding the company vision in actions and demeanor
- Must be able to effectively communicate verbally and in writing
- Must be able to work night Shift – 5:30 pm to 6 am (potential for an occasional day shift but the focus is the night shift)
- Bilingual (English - Spanish) - preferred
- Clinical Research background a plus
Requirements
- Must be a Registered Nurse with a current license in Florida, and not have any disciplinary action on the license
- Must be BLS or ACLS certified or able to obtain
- 0-1 year of experience is required
- Must be IV certified, depending on site
- Must be capable of performing all clinical tasks relevant to licensure and/or training
- Must be able to clearly communicate verbally with patients
- Must have good interpersonal skills, demonstrated through interactions with patients, staff, Sponsor representatives, etc
- Must be self-motivated and able to perform tasks independently
- Ability to react calmly and effectively in emergency situations
- Must reflect the professional image of the company, upholding the company vision in actions and demeanor
- Must be able to effectively communicate verbally and in writing
- Must be able to work night Shift – 5:30 pm to 6 am (potential for an occasional day shift but the focus is the night shift)
- Bilingual (English - Spanish) - preferred
- Clinical Research background a plus
Company overview
CenExel is a leading integrated clinical research site network operating across major metropolitan areas throughout the United States. Founded in 2018 and headquartered in Salt Lake City, Utah, the company operates 18 Centers of Excellence that collectively represent over 40 years of clinical research experience. CenExel specializes in providing comprehensive clinical trial services to pharmaceutical companies, biotechnology firms, and clinical research organizations, with particular expertise in central nervous system (CNS) disorders and early-phase clinical research. The company's nationwide network delivers deep scientific expertise, premium data quality, operational efficiencies, and exceptional patient engagement to drive successful clinical trial outcomes. With more than 1,200 employees across its network, CenExel focuses on accelerating the development of life-changing therapies through its patient-centered approach and commitment to research excellence. The company serves as a strategic partner for sponsors seeking to optimize clinical trial performance, from site selection through study close-out, while maintaining rigorous standards for patient care and scientific integrity.