Jobs
>
New Orleans

    RN Research Coordinator - New Orleans, United States - Ochsner Health

    Ochsner Health
    Ochsner Health New Orleans, United States

    1 week ago

    Default job background
    Full time
    Description
    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

    In coordination and collaboration with principal investigators, evaluates, initiates and maintains all activities related to the conduct of clinical trials in assigned area(s) of responsibility. Communicates effectively with external funding agencies and sponsors, other departments, departmental staff and patients to assure understanding of the requirements of conducting and participating in clinical trials. Organizes and manages all documentation and regulatory submissions as required by the sponsor of the trial, regulatory agencies, Research division / OHS policy and patient care requirements of Ochsner Health System. Provides patient care and assessment as determined necessary by the clinical trial in coordination with other care providers. Functions as project manager for clinical trials in assigned area(s) of responsibility.

    This job collaborates with the multidisciplinary team in the development and delivery of a plan of care as it relates to patient involvement in clinical trials. Practices within the scope of practice defined by the Nurse Practice Act, Code for Nurses and Standards for Nurse Practice.
    Education

    Required - Registered Nurse Dipoma

    Preferred - Masters degree in Nursing, Public Health, and other related clinical /healthcare field

    Work Experience

    Required - 3 years clinical experience

    Preferred- Experience in area of assigned clinical specialty
    Prior experience in clinical research
    Some experience with data entry and data base management

    Certifications

    Required - Current State of Louisiana Registered Nurse License

    Basic Life Support (BLS) from the American Heart Association

    Knowledge Skills and Abilities (KSAs)
    • Must have computer skills and dexterity required for data entry and retrieval of information.
    • Must be proficient with Windows-style applications and keyboard.
    • Effective verbal and written communication skills and the ability to present information clearly and professionally to varying levels of individuals throughout the patient care process.
    • Excellent organizational skills
    • Critical thinking skills to process trial evaluation and submission, particularly the development of study related budgets, contracts and patient consent documents.
    • Self-directed
    Job Duties
    • Coordinates and oversees the regulatory and administrative processes as they relate to the evaluation, initiation, maintenance, closure and internal and external audit of clinical trials and other research activity.
    • Coordinates and provides patient care and assessment as it relates to the conduct of research and clinical trials.
    • Develops and maintains all required documentation as it relates to the conduct of assigned clinical trials and associated patient care.
    • Conducts all activity with regard to the well-being and safety of human subjects enrolled in clinical trials, as well as the general population who will use products of research when approved.
    • Maintains competency in area of clinical expertise and requirements and regulations associated with the conduct of clinical trials and other related research activity.
    • 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.
    Other related duties as required. 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.

    Ochsner 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
    The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.

    Mechanical lifting devices (carts, dollies, etc.) or team lifts should be utilized.
    Must be able to stoop, bend, reach and grab with arms and hands, manual dexterity.
    Must be able to stand for prolonged periods of time.
    Must be able to work a flexible work schedule (e.g. 24/7, weekend, holiday, on call availability).
    Must be able to travel throughout and between facilities.

    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 diseases. There may be an occupational risk for exposure to all communicable diseases.

    Are you ready to make a difference? Apply Today

    Ochsner Health does not consider an individual an applicant until they have formally applied to the open position on this careers website.

    Individuals who reside in and will work from the state of Colorado are not eligible for remote work position.

    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 select option 1) or This contact information is for accommodation requests only and cannot be used to inquire about the status of applications.

    We are proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to the principles of equal employment opportunity and providing a workplace that is free from discrimination based on race, color, creed, religion, pregnancy status, pregnancy-related conditions, national origin, ancestry, mental or physical disability, medical condition, age, veteran status, military status, citizenship status, marital status, familial status, sexual orientation, gender, gender identity or expression, genetic information, political affiliation, unemployment status, or any other characteristic protected under applicable federal, state or local law. These protections extend to applicants and all employment related decisions. View the EEO is the Law poster and its supplement, as well as the pay transparency policy for more information.

    Affirmative Action Policy Statement
  • Tulane University

    Research Coordinator

    1 day ago

    Tulane University New Orleans, United States

    The Research Coordinator coordinates research activities related to multiple projects in the areas of nutrition, food environment research, and policy implementation and evaluation. Activities include assisting in community outreach efforts, program Research Coordinator, Research ...

  • Tulane University

    Research Coordinator

    1 week ago

    Tulane University New Orleans, United States

    The Research Coordinator coordinates research activities related to multiple projects in the areas of nutrition, food environment research, and policy implementation and evaluation. Activities include assisting in community outreach efforts, program planning, graduate assistant t ...

  • Tulane University

    Clinical Research Coordinator

    1 week ago

    Tulane University New Orleans, United States

    The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials in cardiovascular and chronic kidney diseases. The Clinical Research Coordinator assists the investigator team to develop ...

  • Tulane University

    Clinical Research Coordinator

    1 week ago

    Tulane University New Orleans, United States

    Coordinates research projects, clinical trials, and perform duties as required by the protocol. Responsible for recruiting, screening and enrolling patients in study protocols. Obtain medical histories, vital signs, and collect blood samples via veni Research Coordinator, Clinica ...

  • Tulane University

    Clinical Research Coordinator

    1 week ago

    Tulane University New Orleans, United States

    Coordinates all study-related and regulatory processes for the Tulane Cancer Center Office of Clinical Research (TCC OCR) and affiliate sites under the overall direction of the Director of the Clinical Research Office. Responsible for coordinating current and future Oncology rese ...

  • Tulane University

    Clinical Research Coordinator

    1 day ago

    Tulane University New Orleans, United States

    Coordinates all study-related and regulatory processes for the Tulane Cancer Center Office of Clinical Research (TCC OCR) and affiliate sites under the overall direction of the Director of the Clinical Research Office. Responsible for coordinating cu Clinical Research, Research C ...

  • Tulane University

    Clinical Research Coordinator

    1 day ago

    Tulane University New Orleans, United States

    Coordinates research projects, clinical trials, and perform duties as required by the protocol. Responsible for recruiting, screening and enrolling patients in study protocols. Obtain medical histories, vital signs, and collect blood samples via venipuncture. Monitor patients for ...

  • Tulane University

    Research Coordinator, TIES

    1 day ago

    Tulane University New Orleans, United States

    Project TIES is seeking a part-time employee (20 hours/week) to assist study of Social Connectedness and Health among Gender Minority People of Color. This study will examine the social support networks of trans and nonbinary people of color both qua Research Coordinator, Researc ...

  • Tulane University Staff

    Research Coordinator, TIES

    1 week ago

    Tulane University Staff New Orleans, United States

    Project TIES is seeking a part-time employee (20 hours/week) to assist study of Social Connectedness and Health among Gender Minority People of Color. This study will examine the social support networks of trans and nonbinary people of color both qualitatively and quantitatively ...

  • Ochsner Health System

    Clinical Research Coordinator

    1 day ago

    Ochsner Health System New Orleans, United States

    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 f ...

  • Tulane University

    Clinical Research Coordinator

    1 week ago

    Tulane University New Orleans, United States Staff

    Summary · The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials in cardiovascular and chronic kidney diseases. The Clinical Research Coordinator assists the investigator team ...

  • Tulane University

    Clinical Research Coordinator

    1 week ago

    Tulane University New Orleans, United States Staff

    Summary · Coordinates all study-related and regulatory processes for the Tulane Cancer Center Office of Clinical Research (TCC OCR) and affiliate sites under the overall direction of the Director of the Clinical Research Office. Responsible for coordinating current and future On ...

  • Tulane University

    Clinical Research Coordinator

    1 week ago

    Tulane University New Orleans, United States Staff

    Summary · Coordinates research projects, clinical trials, and perform duties as required by the protocol. Responsible for recruiting, screening and enrolling patients in study protocols. Obtain medical histories, vital signs, and collect blood samples via venipuncture. Monitor p ...

  • Tulane University

    Clinical Research Coordinator, CHERISH

    1 day ago

    Tulane University New Orleans, United States

    The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials related to cardiovascular disease. The Clinical Research Coordinator assists the investigator team to develop study protoc ...

  • Tulane University

    Clinical Research Coordinator I

    1 day ago

    Tulane University New Orleans, United States

    The primary responsibility of the Clinical Research Coordinator I is to assist in managing all aspects of conducting clinical trials. The Clinical Research Coordinator I is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by ...

  • Tulane University

    Clinical Research Coordinator I

    1 day ago

    Tulane University New Orleans, United States

    The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials in cardiovascular and chronic kidney diseases. The Clinical Research Coordinator assists the investigator team to develop ...

  • Tulane University

    Clinical Research Coordinator II

    1 day ago

    Tulane University New Orleans, United States

    The Clinical Research Coordinator II will coordinate and conduct the day-to-day operations of TRIAD ongoing studies in cardiovascular diseases. The Clinical Research Coordinator II is required to have an in-depth knowledge of protocol requirements and good clinical practices as s ...

  • Tulane University

    Clinical Research Coordinator, CHERISH

    1 day ago

    Tulane University New Orleans, United States

    The primary responsibility of the Clinical Research Coordinator is to coordinate and conduct the day-to-day operation of clinical studies and clinical trials related to cardiovascular disease. The Clinical Research Coordinator assists the investigato Clinical Research, Research C ...

  • Tulane University

    Clinical Research Coordinator I

    1 day ago

    Tulane University New Orleans, United States

    The primary responsibility of the Clinical Research Coordinator I is to assist in managing all aspects of conducting clinical trials. The Clinical Research Coordinator I is required to have an in-depth knowledge of protocol requirements and good clin Clinical Research, Research C ...

  • Tulane University

    Clinical Research Coordinator III

    1 day ago

    Tulane University New Orleans, United States

    The primary responsibility of the Clinical Research Coordinator III is to manage all aspects of conducting the NIH funded clinical study - the Precision Health Study which is led by Dr. Lu Qi, with minimal supervision. The Clinical Research Coordinat Clinical, Coordinator, Resear ...