Cedars-Sinai Research Nurse - Per Diem - Clinical and Translational Research Center (CTRC) in Los Angeles, California
Do you have a passion for the highest quality and patient happiness? Then please respond to this dynamic opportunity available with one of the best places to work in Southern California! We would be happy to hear from you.
The CTRC supports innovative, patient-oriented research, offers clinical research training and recognition programs and provides researchers an environment for seeing patients when they take part in clinical research studies. The CTRC at Cedars-Sinai was established in 1994 by the National Institutes of Health and funded by the National Center for Advancing Translational Sciences. To learn more, please visit: https://www.cedars-sinai.org/research/clinical/ctrc.html
The CTRC Research Nurse works under direct supervision providing hands-on treatment, monitoring and follow-up clinical analysis of patients participating in clinical trials. This position coordinates all aspects of the CTRC clinical research, including interactions with research personnel and project participants, data-related tasks, IRB prep and submission, grant proposals, and patient recruitment and logistical organization. The Research Nurse will work collaboratively with the Principal Investigator (PI), physicians and other research staff in providing hands-on care in triaging, documenting vitals, administering investigational drugs or interventions, and providing clinical educational services to participants and their families.
Primary Duties and Responsibilities:
Interacts with research participants to provide nursing care, administration of research interventions and specimen collection.
Provides clinical education services to research participants and family regarding study participation, participants current clinical condition, and or disease process.
Monitors research participant and reports potential adverse events to a member of the research team.
Records research data (vital signs, research compound administered, participant responses) in approved source document (medical record, data collection sheet).
Triages patient by phone and provides clinical information to the patient. May also coordinate patient visit to follow up on clinical issues and provide necessary care.
Assist with recruitment and logistics of study participants. Completes and documents study participant enrollment, assessment/reassessment, education, and follow-up activities.
Performs and coordinates study participant interventions as required.
Serves as a liaison between study participant and PI or other research staff.
Prepares data spreadsheets for PI and/or department. Assists with data compilation and documentation.
Adheres to federal and regulatory requirements in providing direct patient nursing care within the context of supporting clinical trial study implementation.
May process, ship, track or otherwise handle research specimens.
Department Specific Responsibilities:
Trained in Human Subjects Protections and oversee research subject compliance requirements per research protocols and according to Cedars-Sinai Institutional Review Board (IRB) requirements
Provides clinical research nursing support and patient care in an outpatient or inpatient setting per research protocol requirements performing vitals, clinical assessments, EKG, infusions, sample collection, etc
Acts as a liaison with Principal Investigators, pharmaceutical company representatives or other project funding organizations to monitor and update project progress
Acts as a liaison with patients’ families and physicians, other project participants, and other research personnel
Coordinates and participates in patient screening, recruitment and scheduling, initiating research patient records, administration of questionnaires, maintaining database Excel spreadsheets, completion of CRF's performing data edits with PI’s, research staff, pharmaceutical company monitors, etc
Demonstrate clinical competence and technical skills necessary to function in the research environment, as such lab skills, blood sample processing, and tissue collection
Demonstrate adequate IV and phlebotomy skills. May provide mobile nurse visits for research purposes to other sites on Cedars-Sinai campus, or surrounding area
Assists with clinical procedures, providing related patient care when required during data collection process
Coordinates and performs daily “interventional” work scheduled for the outpatient facility (CTRC)
Provides nursing care and supervision required by any research subject on inpatient service
Coordinates sample recovery from surgical, surgical pathology, from other clinics, from in-house patients and from outside hospitals and clinics
Collects patient data for PI and other research personnel by taking blood or tissue samples such as phlebotomy, pathological tissues, etc
Process samples including spinning, triaging, etc, or other technical or interactive procedures. May collate data, assist in data analysis or otherwise participate in organizing and determining project findings
Provides back-up for the CTRC Research Nurses in the outpatient duties
Shares evening and weekend on-call responsibilities with the staff of the CTRC
Shares responsibilities of transporting samples, both in-house and offsite
Establishes system for monitoring and maintenance of patient data records
Performs other related duties as assigned or required
Prepares and updates investigation binder and completes CRFs (Case Report Forms)
Associate of Science in Nursing (ASN)/College Diploma Nursing, required
Bachelor of Science in Nursing (BSN), preferred
Valid California RN license and current BLS certification, required
Experience and Skillset:
One (1) year minimum clinical nursing experience required, additional previous research nursing experience is preferred.
Demonstrated commitment to quality service & care, teamwork, and CSMC goals.
Thorough knowledge of nursing techniques in area of research specialization.
Ability to demonstrate the knowledge and skills necessary to provide patient care based on physical/social, education, safety, and related criteria appropriate to the age of the patients served in the CTRC.
Strong interpersonal skills to work effectively with patients, their physicians and/or families; pharmaceutical company representative, and other project personnel.
Must demonstrate excellent communication skills, written and verbal, and have the ability to be consistently accurate, timely and with legibility.
Strong organizational skills to execute all aspects of clinical research, including maintaining patient files, creating database spreadsheets, case report forms, and to be performed in an accurate and timely manner.
Proficient in the establishment and maintenance of intravenous access.
Ability to work in a fast paced, high volume environment with frequent interruptions and multiple demands.
Cedars-Sinai is an EEO employer. Cedars-Sinai does not unlawfully discriminate on the basis of the race, religion, color, national origin, citizenship, ancestry, physical or mental disability, legally protected medical condition (cancer-related or genetic characteristics or any genetic information), marital status, sex, gender, sexual orientation, gender identity, gender expression, pregnancy, age (40 or older), military and/or veteran status or any other basis protected by federal or state law.