RN Clinical Researcher

Job Overview 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 communicates with external funding agencies, sponsors, departments, and patients to ensure understanding of the requirements of conducting and participating in clinical trials. It organizes and manages all patient care requirements and provides patient care and assessment as determined necessary. Education Associate degree in nursing. Work Experience 3 years of experience in 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. Basic Life Support (BLS) from the American Heart Association. Knowledge, Skills, and Abilities (KSAs) Effective verbal and written communication skills and ability to present 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 and ability to work independently and in a team environment. Ability to follow and provide critical feedback on the investigational plan. Ability to train junior staff members on standard operating procedures and other related research activities. Strong organizational and time management skills and ability to multi‑task, pay close attention to detail, and learn new techniques. Strong working 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 and dose modifications, treatment plan, associated required tests and procedures, and all other aspects of the protocol as required. Knowledge and execution of the nursing process to assess toxicities from investigational therapies and work with the investigator in management of these adverse events. Working knowledge in using computers, software, and web‑based applications, including Epic. Ability to travel throughout and between facilities and work a flexible work schedule, including on‑call, weekend, and night shifts, as required. Job Duties Participates in clinical trial selection with research leadership and organizes strategies for recruiting study participants and screening study participants for eligibility on the telephone, in the clinic, and other settings as required. Uses the nursing process to ensure protocol compliance including but not limited to patient recruitment, engaging in informed consent, patient education, & oversight of investigational drug administration schedule and conducts daily work and clinical trial activity in accordance with Good Clinical Practice Guidelines. Coordinates and oversees patient (study participant) activity as it relates to the conduct of research and clinical trials, serving as a liaison for both patient and the private investigator (PI) and monitors patients for safety and adverse events during medical procedures, including administration of parenteral investigational agents depending on area of assignment. Assists in disbursement of oral investigational drugs, provides patient teaching regarding administration, and educates patients and family members about protocols including risks and benefits of participation, potential side‑effects, and self‑administration of drugs. Completes and/or supervises staff for the completion of case report forms on assigned protocols within the time frame required by the study and works in partnership with regulatory team to ensure appropriate credentialing, training, and maintenance of regulatory documents in accordance with SOP and applicable regulations. Oversees and/or conducts basic lab duties including centrifuging, aliquoting, and storing and shipping of study specimens. Completes data entry into sponsor‑specific data entry systems and/or supports data coordinator, including query resolution and transcribes information across various internal and external electronic data systems. Trains less senior team members and interns and identifies ongoing professional development needs and seeks resources and opportunities to meet those needs. Adapts behavior to the specific patient population, including but not limited to respect for privacy, method of introduction to the patient, adapting explanation of services or procedures to be performed, requesting permissions and communication style. Performs other related duties as assigned. Physical and Environmental Demands Medium work: Exerting 20 to 50 pounds of force occasionally, and/or 10 to 25 pounds of force frequently, and/or greater than negligible up to 10 pounds of force constantly to move objects. Duties involve walking or standing for significant periods and the possibility of pushing or pulling objects. Exposure to blood, body fluid and tissue and communicable disease risk is inherent to the role. Potential exposure to hazardous medications or waste, including receipt, transport, storage, preparation, dispensing, administration, cleaning and disposal, exists and may vary by specific duties. EEO Statement The employer 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 Ochsner Health