Sr RN Clinical Research - Oncology

Ochsner Health; New Orleans (LA); On-site; USD 75,000 - 110,000; Full time

Job summary

Ochsner Health in New Orleans seeks an experienced Clinical Trial Nurse to evaluate, initiate, and maintain all activities related to the conduct of clinical trials. You will communicate with sponsors and staff to ensure understanding of trial requirements and coordinate patient care.

The role requires an RN license, an Associate degree in nursing with 5 years of clinical specialty experience including 3 years in clinical research, and BLS certification.

Qualifications

• RN license required in state of practice.
• Associate degree in nursing required; bachelor's preferred.
• 5 years in area with 3 years in clinical research or 4 years with relevant nursing certification (ACRP/SOCRA).

Responsibilities

• Participates in clinical trial selection with research leadership and evaluates strategies for recruiting study participants.
• Uses the nursing process to ensure protocol compliance including patient recruitment, informed consent, and education.
• Coordinates and oversees patient activity related to research, serving as liaison for patients and investigators and monitoring safety.
• Mentors junior staff and assists with onboarding and inter-department communication.
• Performs data entry into sponsor systems and supports data coordinators.
• Actively participates in quality improvement efforts and ensures data integrity.
• Adapts behavior to patient populations and maintains privacy.
• Performs other duties as assigned.

Skills

Nursing

Clinical Research

Leadership

Communication

Education

Associate degree in nursing

Bachelor's degree in nursing

Tools

Epic

Job description

Exceptional care starts with exceptional people. For us, this is more than a job– it’s a calling. It’s waking up each day, looking for ways to make a difference with a compassionate, inclusive and talented team. Ochsner empowers you to discover your passion, reach your potential, and Pursue Your Purpose. Exceptional care starts with exceptional people and teams. Together we are leading the way. This job evaluates, initiates, and maintains all activities related to the conduct of clinical trials. Communicates with external funding agencies, sponsors, departmental staff, and patients to ensure the understanding of the requirements of conducting and participating in clinical trials. Independently organizes and manages all patient care requirements of the company. Serves as an escalation point for junior level departmental staff for problem resolution and support, and typically coordinates trials that are the most complex and/or the greatest number of trials. To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential duties. This job description is a summary of the primary duties and responsibilities of the job and position. It is not intended to be a comprehensive or all-inclusive listing of duties and responsibilities. Contents are subject to change at the company’s discretion.

Education

Required - Associate degree in nursing.

Work Experience

Preferred - Bachelor's or degree in nursing

Required - 5 years of experience in area of assigned clinical specialty including 3 years performing clinical research, or 4 years of relevant research experience in a clinical setting with ACRP, SOCRA, or relevant professional nursing certification.

Certifications

Required - Current registered nurse (RN) 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.
• Expert understanding of ICH guidelines for ethical conduct of research.
• Ability to follow and provide critical feedback on the investigational plan.
• Familiarity with and understanding of lean management principles.
• Ability to mentor junior staff members on the requirements and regulations associated with the conduct of clinical trials and other related research activities.
• 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.
• Expertise in using computers and web-based applications including working knowledge of Epic (Super-Users).
• Strong foundation with respect to regulatory processes and requirements for all phases of research.
• Strong interpersonal and leadership skills and ability to mentor junior staff members on the requirements and regulations associated with the conduct of clinical trials and other related research activity.
• Ability to travel throughout and between facilities and work a flexible work schedule, including on-call, weekend, and night shifts, shifts depending on area of assignment.

Job Duties

• Participates in clinical trial selection with research leadership and evaluates competing 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.
• 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 PI and monitors patients for safety and adverse events during medical procedures, including administration of parenteral investigational agents depending on area of assignment and with appropriate training and certification.
• Coordinates special projects related to workflow optimization, periodically reviews, and provides constructive feedback on standard operating procedures and communicates clinical information and work with stakeholders to create best practice tools.
• Provides mentorship, professional development, and support to less senior team members and interns and assists in precepting new hires and working with leadership to ensure inter-departmental communication and timely departmental onboarding.
• 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 and serves as a resource for data entry to junior team members.
• Actively participates in the department’s quality improvement efforts, identifies opportunities for quality improvement to colleagues and management, provides leadership to the research team ensuring collection of source data and documentation that validated integrity of research, and assesses quality assurance of study visits and data.
• Identifies ongoing professional development needs and seeks resources and opportunities to meet those needs (nursing organizations, independent classes, lectures, etc.)
• 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.

The above statements describe the general nature and level of work only. They are not an exhaustive list of all required responsibilities, duties and skills. Other duties may be added, or this description amended at any time.

Remains knowledgeable on current federal, state, and local laws, accreditation standards or regulatory agency requirements that apply to the assigned area of responsibility and ensures compliance with all such laws, regulations, and standards.

This employer maintains and complies with its Compliance & Privacy Program and Standards of Conduct, including the immediate reporting of any known or suspected unethical or questionable behaviors or conduct; patient/employee safety, patient privacy, and/or other compliance-related concerns.

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.

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. (Constantly: activity or condition exists 2/3 or more of the time) to move objects. Physical demand requirements are in excess of those for Sedentary Work. Even though the weight lifted may be only a negligible amount, a job should be rated Light Work: (1) when it requires walking or standing to a significant degree; or (2) when it requires sitting most of the time but entails pushing and/or pulling of arm or leg controls; and/or (3) when the job requires working at a production rate pace entailing the constant pushing and/or pulling of materials even though the weight of those materials is negligible. NOTE: The constant stress and strain of maintaining a production rate pace, especially in an industrial setting, can be and is physically demanding of a worker even though the amount of force exerted is negligible.
Duties performed routinely require exposure to blood, body fluid and tissue.
The incumbent works in a patient care area; works in an area where patients enter; works directly with patients; and/or works with specimens that could contain communicable diseases.
Because the incumbent works within a healthcare setting, there may be occupational risk for exposure to hazardous medications or hazardous waste within the environment through receipt, transport, storage, preparation, dispensing, administration, cleaning and/or disposal of contaminated waste. The risk level of exposure may increase depending on the essential job duties of the role.

Individuals who reside in and will work from the following areas are not eligible for remote work position: Colorado, California, Hawaii, Illinois, Maine, Maryland, Massachusetts, Minnesota, New Jersey, New York, Vermont, Washington, and Washington D.C.

Ochsner Health endeavors to make our site accessible to all users. If you would like to contact us regarding the accessibility of our website, or if you need an accommodation to complete the application process, please contact our HR Employee Solution Center at 504-842-4748 (select option 1) or [e-mail]. This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.