Sr Research Nurse

Are you passionate about the patient experience? At HCA Healthcare, we are committed to caring for patients with purpose and integrity.

HCA Healthcare Research Institute is the multispecialty clinical research arm of HCA Healthcare. Our expert physicians work with trusted pharmaceutical and biotechnology partners to unlock insights from real-world data and conduct clinical studies leading to breakthroughs in science, medicine and care for all people. Today's research paves the way for tomorrow's breakthroughs. Consider joining our HCA Healthcare Research Institute today!

Senior Research Nurse is responsible for coordinating multiple research protocols; serving as a liaison withlocal investigators and local research personnel; and acting as a central resource for assigned research projects. This individual seeks to demonstrate a moderate to advanced level of independence when performing research coordination duties and can apply skills to a broad range of study types.
This role is hospital based.

What you will do in this role:

• 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)
• Maintain a strong understanding of state guidelines and regulatory standards
• 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
• Re-consent patients in a timely manner and document process appropriately Site Development:
• Work with site personnel and local investigators to assess site feasibility and performance
• Regularly meet with physician investigators, when applicable, to assess study performance and site satisfaction
• Create and support a climate of trust, openness and honest communication
• Collaborate with other departments (non-invasive, finance, laboratory, etc.) to develop and implement processes in support of the research activities
• Facilitate continuing education and training to investigators, as applicable
• Practice and adhere to the “Code of Conduct” philosophy and “Mission and Value Statement”
• Ability to satisfy all responsibilities of the Research Nurse Job Description

What qualifications you will need:

• Bachelor’s Degree required
• Active RN License required
• 3+ years of relevant research experience preferred
• Knowledge of federal regulations, good clinical practices (GCP)
• Knowledge of medical and research terminology
• Computer skills including use of clinical trial database, electronic data capture, and MS Word or Excel
• Excellent Verbal and written communication skills
• Excellent interpersonal skills
• The ability to communicate