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Clinical Research RN - FL

Trinity, FL 34655

Posted: 01/21/2025 Industry: Healthcare Job Number: 21235

Job Description


 

Rezult Group continues to make great strides toward enhancing patient care through technology services nationwide. We are consistently looking for qualified professionals to join us in achieving success. Currently we are searching for a Clinical Research Registered Nurse to fulfill an immediate contract vacancy in Trinity, FL and Brandon, FL.

 

 

·      The Research Nurse is responsible for coordinating multiple research protocols and serving as a liaison with local investigators, clinical staff, and research personnel. Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a strong fundamental understanding of human subject research.

·      Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement”

·      During your employment with HRI you will be routinely assigned training requirements. You are expected to complete any training assignments by the due date.

·      Complete study medication order forms accurately, when needed, and has physician or appropriate designee sign orders prior to medication administration

·      Perform routine operational activities for multiple research protocols • Liaise between site research personnel, industry sponsors, and Supervisor

·      Collaborate closely with various site departments/teams, including finance, relevant hospital administrative representatives, and the local IRB, if applicable

·      Coordinate protocol schedule of assessments from initial submission of feasibility until study closeout

·      Coordinate submission and approval for the Site’s Facility Review Committee, if applicable

·      Provide instruction on research protocols to appropriate staff, including interpretation of test results, observations, and related study data to physicians, nurses, and clinical staff

·      Assess the patient and document findings at each clinic visit while on protocol

·      Document all specific tasks required by the protocol (i.e. medication forms, quality of life questionnaires, neuro exams, vital signs sheets, times of lab draws, etc.)

·      Complete the study medication order form accurately and have the physician or nurse practitioner sign orders prior to treatment

·      Ensure that all medications are approved by the appropriate designee prior to initiating treatment or when changing medication regimens

·      Accurately calculate and document the BSA, creatinine, STS calculation, or any other conversions needed, per protocol

·      Document any interaction regarding the patient that occurs while the patient is enrolled on a protocol, including follow-up and survival (this includes home health intervention, pharmacies, and patient phone calls)

·      Ensure that follow-up appointments, imaging, or any related procedures are scheduled correctly according to protocol requirements

·      Accurately complete all data requests (including queries) and submit with source documentation within the timeframe specified in the SOP

·      Generate and track drug shipments, device shipments, and supplies as needed

·      Ensure timely and accurate data completion

·      Track and report adverse events, serious adverse events, protocol waivers, deviations, and violations • Communicate all protocol-related issues to appropriate study personnel or manager

·      Re-consent patients in a timely manner and document process appropriately

 

 

We are actively speaking with applicants that have a minimum of:

 

·      1+ year of experience in patient care setting; proficient in various electronic applications, Microsoft Office, EDC, CTMS; knowledge of basic medical terminology required. Must have strong knowledge of Good Clinical Practices.

·      Registered Nurse - Currently licensed as a registered professional nurse in the state in which he or she practices, in accordance with law and regulation.

·      Knowledge of organizational policies, standard operating procedures, and systems.

·      Emerging understanding and application of ICH guidelines and the Code of Federal Regulations within the clinical research environment.

·      Working knowledge of medical and clinical research terminology.

·      Demonstrate competency in EKG acquisition, phlebotomy, and other clinical tasks within nursing scope of work, as needed per licensure.

·      Maintain HIPAA compliance knowledge and adhere to all HIPAA regulations, per HRI SOPs.

·      Schedule: Monday- Friday - 5am - 1 pm

 

 

If your background, skills, and interest match the following; please apply online to ensure your credentials are reviewed by a skilled recruiter immediately. We look forward to working with you on this opportunity. For more information on Rezult Group and a list of additional job openings, please visit our website at www.rezultgroup.com.

 

 

 
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About Trinity, FL

Ready to discover exciting job opportunities in the vibrant area surrounding Trinity, Florida? Nestled in the heart of Pasco County, this charming region offers a unique combination of urban amenities and natural beauty, making it an ideal location to grow your career. With easy access to stunning beaches like Anclote Key Preserve State Park and vibrant cultural hotspots like the Tarpon Springs Sponge Docks, Trinity boasts a diverse and enriching lifestyle. Explore job listings in this flourishing area and unlock your potential for success in a community that values both professional growth and quality of life. Join us in Trinity, FL, where career fulfillment meets captivating surroundings!

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