RN Clinical Researcher

We’ve made a lot of progress since opening the doors in 1942, but one thing has never changed - our commitment to serve, heal, lead, educate, and innovate. We believe that every award earned, every record broken and every patient helped is because of the dedicated employees who fill our hallways. At Ochsner, whether you work with patients every day or support those who do, you are making a difference and that matters. Come make a difference at Ochsner Health and discover your future today! This position evaluates, initiates, and maintains all activities related to the conduct of clinical trials in assigned area(s) of responsibility in coordination and collaboration with principal investigators. The role involves communications with external funding agencies, sponsors, departments, and patients to ensure compliance with requirements of conducting and participating in clinical trials. The incumbent organizes and manages patient care requirements, provides patient care and assessment as determined necessary by the clinical trial, and coordinates all aspects of trial logistics in partnership with care providers. Education Associate degree in nursing (required). Work Experience 3 years of experience in area of assigned clinical specialty, including 2 years performing clinical research, or 2 years of relevant research experience in a clinical setting with ACRP, SOCRA, or relevant professional nursing certification. Certifications Current registered nurse license in state of practice (required). Basic Life Support (BLS) from the American Heart Association (required). Knowledge, Skills, and Abilities Effective verbal and written communication skills, presenting information clearly and professionally to varying levels of individuals throughout the patient care process. Working knowledge of ICH guidelines for ethical conduct of research. Strong problem‑solving and critical‑thinking skills, ability to work independently and in a team environment. Ability to follow and provide critical feedback on the investigational plan. Training junior staff on standard operating procedures and other related research activities. Strong organizational and time‑management skills, ability to multitask, pay close attention to detail, and learn new techniques. Knowledge of the requirements and regulations associated with the conduct of clinical trials and other related research activity. Ability to interpret and carry out all aspects of a protocol, including patient eligibility, assessing adverse events, dose modifications, treatment plans, required tests and procedures, and all other protocol requirements. Execution of the nursing process to assess toxicities from investigational therapies and coordination with investigators in management of adverse events. Working knowledge of computers, software, and web‑based applications, including Epic. Willingness to travel within and between facilities and work a flexible schedule, including on‑call, weekend, and night shifts as required. Job Duties Participate in clinical trial selection with research leadership, organize strategies for recruiting study participants, and screen participants for eligibility via telephone, in clinic, and other settings. Use the nursing process to ensure protocol compliance, including patient recruitment, informed consent, patient education, oversight of investigational drug administration schedule, and conduct daily activity in accordance with Good Clinical Practice Guidelines. Coordinate and oversee patient activity related to research and clinical trials, serve as liaison for patients and investigators, monitor patients for safety and adverse events during medical procedures, and administer parenteral investigational agents as needed. Assist in the disbursement of oral investigational drugs, provide patient teaching on administration, and educate patients and families about protocol risks, benefits, potential side‑effects, and self‑administration. Complete and/or supervise staff in completing case report forms on assigned protocols within required time frames, and collaborate with regulatory team to maintain credentialing, training, and regulatory documents according to SOP and regulations. Oversee or conduct basic laboratory duties, including centrifuging, aliquoting, storing, and shipping study specimens. Enter data into sponsor‑specific data entry systems, support data coordinators, resolve queries, and transcribe information across internal and external electronic data systems. Train less senior team members and interns, identify professional development needs, and seek resources to meet those needs. Adapt communication style to specific patient populations, respecting privacy and tailoring explanations of services or procedures. Perform other related duties as assigned. Physical & Environmental Demands Medium work: moving light to moderate weight objects occasionally or frequently. Exposure to blood, body fluids, and tissue. Work in a patient care area with potential exposure to communicable diseases and hazardous medications or waste. Suitable for individuals with the ability to perform these tasks. Equal Opportunity Employer Ochsner Health is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, or disability status. #J-18808-Ljbffr Council of State and Territorial Epidemiologists