- 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 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 works with the investigator in management of these adverse events.
- Working knowledge in using computers, software, and web-based applications, including working knowledge of Epic.
- 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.
- 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 his/her 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.
-
clinical research
2 weeks ago
LSU Health Sciences Center New Orleans, United StatesPosting Details · Posting Summary Functional Position Title CLINICAL RESEARCH / DENTAL ASSISTANT Position Number Appointment Type Period of Appointment Location-City New Orleans School/Division LSUNO DENTISTRY Department LSUNO Prosthodontics Position Summary This position requir ...
-
Clinical Research Coordinator
1 week ago
Tulane University New Orleans, United States StaffSummary · The primary responsibility of the Clinical Research Coordinator II is to coordinate and conduct the day-to-day operation of clinical trials and other epidemiological studies. The Clinical Research Coordinator II is required to have knowledge of protocol requirements an ...
-
Clinical Research Coordinator
6 days ago
Tulane University New Orleans, United States StaffSummary · 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 ...
-
Clinical Research Coordinator
4 days ago
Tulane University New Orleans, United StatesCoordinates 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 ...
-
Clinical Research Coordinator
3 weeks ago
Tulane University New Orleans, United StatesCoordinates 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 ...
-
Clinical Research Coordinator
1 week ago
Tulane University New Orleans, United StatesThe 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 ...
-
Clinical Research Coordinator
4 days ago
Tulane University New Orleans, United StatesThe 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 Clinical, Research, Coordinat ...
-
Clinical Research Coordinator
1 week ago
Tulane University New Orleans, United StatesThe primary responsibility of the Clinical Research Coordinator II is to coordinate and conduct the day-to-day operation of clinical trials and other epidemiological studies. The Clinical Research Coordinator II is required to have knowledge of proto Clinical Research, Research C ...
-
Clinical Research Coordinator
4 days ago
Tulane University New Orleans, United StatesCoordinates 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 ...
-
Clinical Research Coordinator
3 weeks ago
Ochsner Health System New Orleans, United StatesWe'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 ...
-
Clinical Research Coordinator
3 weeks ago
Tulane University New Orleans, United StatesCoordinates 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 ...
-
Senior Clinical Research
3 weeks ago
Tulane University New Orleans, United StatesThe primary responsibility of the Senior Clinical Research Coordinator is to manage the daily operations of the study data and coordinating center for a hypertension control project taking place in Jamaica and Colombia. The Senior Clinical Research Coordinator is required to have ...
-
Clinical Research Assistant
11 hours ago
SQRL Marrero, United StatesHighlights · Play a key role in helping patients get involved in clinical trials · up to $50,000 salary + full benefits · Monday - Friday; no weekends · Growth opportunities to CRC, Sr. CRC, and more · Great stepping stone into research, or a way to get more experience · The Com ...
-
Clinical Research Coordinator I
3 weeks ago
Tulane University New Orleans, United StatesThe 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 ...
-
Clinical Research Recruitment Specialist
4 days ago
DelRicht Research New Orleans, United StatesWhy DelRicht Research? · Would you love to be a part of the cutting edge of healthcare and science innovation? Do you want to be an influential part of a rapidly growing team? Are you looking for a position that has sustainable opportunity for professional growth? If the answer i ...
-
Clinical Research Recruitment Specialist
8 hours ago
Delricht Research New Orleans, United StatesJob Description · Job DescriptionSalary: $33,000-$50,000 · Why DelRicht Research? · Would you love to be a part of the cutting edge of healthcare and science innovation? Do you want to be an influential part of a rapidly growing team? Are you looking for a position that has susta ...
-
Clinical Research Coordinator II
5 days ago
Tulane University New Orleans, United StatesThe 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 ...
-
Clinical Research Coordinator, CHERISH
3 weeks ago
Tulane University New Orleans, United StatesThe 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 ...
-
Clinical Research Coordinator, CHERISH
3 weeks ago
Tulane University New Orleans, United StatesThe 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 ...
-
Clinical Research Coordinator III
3 weeks ago
Tulane University New Orleans, United StatesThe 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 ...
RN Clinical Research - New Orleans, LA, United States - Ochsner Health
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
This job 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. Communicates with external funding agencies, sponsors, departments, and patients to ensure understanding of the requirements of conducting and participating in clinical trials. Organizes and manages all patient care requirements. Provides patient care and assessment as determined necessary by the clinical trial in coordination with other care providers.
Education
Required - Associate degree in nursing.
Work Experience
Required - 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
Required - Current registered nurse license in state of practice.
Basic Life Support (BLS) from the American Heart Association.
Knowledge Skills and Abilities (KSAs)
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
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.
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. The incumbent has an occupational risk for exposure to all 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.
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 following areas are not eligible for remote work position: Colorado, California, Washington, and New York.
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
