Current jobs related to Clinical Trial Research Nurse I - El Sobrante - Kaiser
-
Clinical Research Nurse I
18 hours ago
El Dorado, Arkansas, United States University of Arkansas System Full timeJob SummaryThe University of Arkansas System is seeking a highly skilled and experienced Clinical Research Nurse to join our team. As a Clinical Research Nurse, you will play a critical role in the coordination of clinical trials, ensuring the smooth execution of research studies and providing exceptional patient care.Key ResponsibilitiesCoordinate...
-
Cardiology Research Associate I
3 days ago
El Segundo, California, United States CEDARS-SINAI Full timeJob SummaryCedars-Sinai is seeking a highly motivated and detail-oriented Cardiology Research Associate I to join our team. As a key member of our research team, you will be responsible for coordinating and implementing clinical trials, ensuring compliance with protocol and research objectives, and providing exceptional patient care.Key...
-
Clinical Trials Nursing Specialist
2 weeks ago
El Dorado, Arkansas, United States University of Arkansas System Full timeJob Title:Clinical Trials Nursing SpecialistCompany:University of Arkansas SystemOverview:Oversee the coordination of activities related to patients involved in clinical research studies.Independently manage the operations of clinical trials.Apply nursing methodologies for procedures associated with studies.Act as a representative for the organization in the...
-
Clinical Research Associate I CS_PER_DIEM
2 months ago
El Segundo, United States CEDARS-SINAI Full timeJob DescriptionWhen the work you do every single day has a crucial impact on the lives of others, every effort, every detail, and every second matters. This shared culture of happiness, passion, and dedication pulses through Cedars-Sinai. With a team focused on effective pain management and quick recovery, Cedars-Sinai has been ranked as the No. 1 hospital...
-
El Paso, United States Parexel Full timeJob Summary:The Clinical Research Associate is the clinical sites' direct point of contact and accountable for managing site quality and delivery from site identification through close-out. The aim of this role is to build the relationship with the site, to be the sole position accountable for the site performance, including driving the site successfully to...
-
Hematologist/Oncologist - NEXT Oncology El Paso
2 months ago
El Paso, United States American Society of Clinical Oncology Full timeNEXT Oncology , a globally recognized leader in Phase I Oncology research and a division of Texas Oncology , is growing. We are looking to add a physician in the El Paso market where they will share space with 10 other Hematologist/Oncologists with Texas Oncology. This organization works in direct patient care by identifying and managing patients appropriate...
-
Research Associate IV
2 months ago
El Monte, United States CEDARS-SINAI Full timeJob Description Come join our team! Under general guidance, the Research Associate IV manages all lab activities including financial management (preparation of and compliance with grant proposals), human resource management and general administration. Responsible for compliance with safety standards and procedures for working with hazardous materials and...
-
Research Grant Specialist I
7 days ago
El Segundo, California, United States CEDARS-SINAI Full timeAbout the RoleCedars-Sinai is seeking a highly skilled Research Grant Specialist I to join our team in the Department of Neurology. As a key member of our research team, you will play a critical role in supporting the Principal Investigator and research staff in the administration of research grants.Key Responsibilities:Monitor and manage research grant...
-
Intake Specialist I
4 weeks ago
El Sobrante, United States Center for Elders Independence Full timeDescription The Position: The Intake Specialist I (IS I) will navigate the intake/enrollment process and introduce the participant to their designated center IDT for capitation. They will work with the Enrollment Development Representative (EDR) to assist in increasing the PACE program membership and drive overall census growth by effectively enrolling...
-
Senior Clinical Research Associate, Field Monitor
2 months ago
El Segundo, United States ImmunityBio Full timeCompany Overview ImmunityBio, Inc. (NASDAQ: IBRX) is a commercial-stage biotechnology company developing cell and immunotherapy products that are designed to help strengthen each patient's natural immune system, potentially enabling it to outsmart the disease and eliminate cancerous or infected cells. We envision a day when we no longer fear cancer, but can...
-
El Segundo, California, United States L'OREAL GROUP Full timeRole: Director- Scientific Liaison for Communications, Clinical Research & InnovationBrand: skinbetter scienceLocation: El Segundo, CADivisional Overview:At Loreal Dermatological Beauty (LDB), we make a difference to the lives of millions of consumers by improving the health and beauty of their skin, through every stage of life. Our brands (CeraVe,...
-
Clinical Research Psychologist
6 days ago
El Cajon, California, United States Leidos Full timeOverview:Are you seeking a fulfilling career that contributes to the well-being of military personnel? Leidos is currently looking for a Clinical Research Psychologist to support the Operational Readiness Directorate. This role is pivotal in enhancing the health, readiness, and overall quality of life for service members. Key Responsibilities:This position...
-
Program Specialist I
6 days ago
El Paso, Texas, United States Texas A&M Agrilife Research Full timeProgram Specialist IWe are seeking a highly skilled and dedicated Program Specialist I to contribute to the development and implementation of innovative programs and services at Texas A&M Agrilife Research.Key Responsibilities:Program Development: Assist in planning, developing, and implementing programs and services that meet the needs of our community,...
-
Clinical Nurse Manager
2 weeks ago
El Paso, Texas, United States Clinical Management Consultants Full timePosition OverviewA prominent acute care facility is actively seeking a Clinical Nurse Manager for their Medical Surgical department. This esteemed organization is dedicated to delivering comprehensive healthcare services to the community, encompassing a wide range of inpatient, outpatient, and specialized care.The Clinical Nurse Manager will play a pivotal...
-
Teachers at El Sobrante KinderCare
2 months ago
El Sobrante, United States KinderCare Education Full timeFutures start here. Where first steps, new friendships, and confident learners are born. At KinderCare Learning Companies, the first and only early childhood education provider recognized with the Gallup Exceptional Workplace Award, we offer a variety of early education and child care options for families. We pave the way for their lifelong learning journey...
-
Registered Nurse Clinical Coord Progressive Care
2 months ago
El Paso, United States Del Sol Medical Center Full timeDescription IntroductionAre you looking for a place to deliver excellent care patients deserve? At Del Sol Medical Center we support our colleagues in their positions. Join our Team as a(an) Progressive Care RN Clincical Coordinator and access programs to assist with every stage of your career.BenefitsDel Sol Medical Center, offers a total rewards package...
-
Registered Nurse Clinical Coord Progressive Care
4 weeks ago
El Paso, United States Del Sol Medical Center Full timeDescription IntroductionAre you looking for a place to deliver excellent care patients deserve? At Del Sol Medical Center we support our colleagues in their positions. Join our Team as a(an) Progressive Care RN Clincical Coordinator and access programs to assist with every stage of your career.BenefitsDel Sol Medical Center, offers a total rewards package...
-
Teachers at El Sobrante KinderCare
3 months ago
El Sobrante, United States KinderCare Education Full timeJob DescriptionFutures start here. Where first steps, new friendships, and confident learners are born. At KinderCare Learning Companies, the first and only early childhood education provider recognized with the Gallup Exceptional Workplace Award, we offer a variety of early education and child care options for families. We pave the way for their lifelong...
-
Clinical Lab Scientist I, Special Testing Lab
2 months ago
South El Monte, United States CEDARS-SINAI Full timeJob Description Do you have a passion for the highest clinical quality and patient happiness? Would you like to use your clinical competencies with an organization known nationally for excellence in cancer treatment, research, and education? We would be happy to hear from you! Please consider the following exciting opportunity with one of the most...
-
Child Psychologist
3 days ago
El Sobrante, California, United States Kaiser Full timeJob Summary:As a Child Psychologist in our Intensive Outpatient Program (IOP) - Psychiatry, you will provide mental health assessment, diagnosis, treatment, and crisis intervention services for children and adolescents who present with a broad range of mental health needs. You will collaborate with a multidisciplinary team to plan and direct each...
Clinical Trial Research Nurse I
2 months ago
The Clinical Trial Nurse I (CTN-I) is a novice level position which, under the guidance and supervision of the Principal Investigator (PI) and clinical trials administrative management, assists in ensuring that the integrity and quality of the clinical trial(s) are maintained and conducted in accordance with federal, state and local regulations, Institutional Review Board (IRB) approvals, and Kaiser Permanente (KP) policies and procedures. With direction from the PI, this position coordinates research activities as outlined in the Major Responsibilities below. This position is also responsible for protecting the health, safety, and welfare of research participants. Essential Responsibilities:
- Compliance
- Support and comply with the Principles of Responsibility (Kaiser Permanente Code of Conduct). With guidance from PI, assist with ensuring compliance with KPNC IRB approved protocols.
- Adhere to Guideline for Good Clinical Practice (GCP), federal, state and local regulations, and KP policies and procedures. With direction, assist with any internal/external compliance monitoring and/or audits and inspections to protect research participants, assure operational effectiveness of the program, and to reduce risks to the organization.
- Study Implementation
- With guidance from PI, utilize nursing skills to coordinate research-related activities (e.g., scheduling study visits, assisting with nursing assessment of participants, adverse events, and data collection including laboratory and diagnostic studies).
- Perform nursing procedures required in the protocol, and report all protocol violations/deviations and averse events to the PI in a timely manner to ensure the health, safety and welfare of the participants.
- With supervision, utilize and document the nursing procedures to plan, deliver, and evaluate research care for non-complex medical conditions and, with appropriate assistance, for complex medical conditions.
- With supervision and direction by PI and/or designee, plan recruitment procedures for potential participants.
- Assist in the determination of eligibility of candidates for study participation.
- Assist in the identification and procurement of equipment and supplies needed to fulfill protocol requirements.
- With supervision, assist in the enrollment of subjects into the trial (screening, randomization, data collection) and any study-related procedures as required by protocol.
- With direction from PI, continuously assess participants to ensure continued eligibility for participation in the study.
- Participate in the ongoing informed consent process with the PI to ensure that research participants and their families have their questions answered and understand the patient/participant Bill of Rights, consent form, and participants responsibilities in the study.
- With direction, communicate with participants throughout the study regarding pertinent updated study information.
- Accurately and completely record information in source documents in a timely manner.
- With supervision, assist in the accurate and appropriate study test article management.
- Coordinate and perform packaging and shipping of protocol specimens to the Sponsor lab in accordance with IATA/DOT regulations and Sponsor shipping guidelines, if applicable.
- Within the nursing scope of practice, assist the PI with the care and evaluation of research participants.
- With direction, abstract data from source documentation onto case report forms (paper or electronic) in a timely manner.
- Assist with study completion, resolution of data queries, data lock, study closeout, and archiving of study files.
- Support the regulatory team in the maintenance and storage of critical documents required to be maintained and provided to the Sponsor during the conduct of the trial.
- Support the effective financial management of the clinical trial.
- Leadership and Communication
- With guidance from the PI, communicate with and educate the research participant about study activities and requirements, as needed.
- Collaboratively participate in study team meetings.
- With supervision, maintain ongoing communication with internal and external parties, Sponsor, PI, clinical trials administrative management, study participants, and KPNC Offices of Clinical Trial Compliance and Operations.
- If applicable and with supervision, coordinate IRB communications (e.g., new protocols, amendments, continuing review applications, protocol violations, and adverse events) in accordance with institutional and departmental policies and procedures.
- Education and Training
- With direction, participate in training, education, and development activities to improve own knowledge and performance to sustain and enhance professional development as a novice research nurse participating in the conduct of clinical trials.
- Work with an assigned mentor on a regular basis for training and resource questions. Attend KP site-initiated meetings for protocol training including Sponsor-initiated meetings, as requested.
- Participate as a member of the Clinical Trial Operations Team (CTOT) and attend meetings, as requested.
- Quality Improvement
- With direction, perform routine quality control activities and assist with quality improvement initiatives.
- Systems and Infrastructure
- Adhere to departmental policies and procedures to ensure confidentiality, privacy and security of clinical research interactions and participant information, and responsible use of operational research databases in compliance with KP policies. Adhere to departmental policies and procedures to support high-quality implementation and conduct of clinical trials, and assure maintenance of research activities and documentation in compliance with the protocols and KP policies and procedures.
- Assist others with the maintenance of systems and resources for the effective communication and submission of required documentation to the IRB.
- Participate with PI and KFRI to identify and prioritize the development of clinical trials systems and infrastructure to maintain research quality and compliance at clinical trial sites.
- Staff Supervision
- No supervisory responsibilities. May oversee specific tasks of non-licensed clinical trial research staff and provide feedback to supervisor.
- General
- Perform job functions according to the factors listed below under Job Criteria.
- Other duties as assigned by appropriate management.
- Kaiser Permanente conducts compensation reviews of positions on a routine basis. At any time, Kaiser Permanente reserves the right to reevaluate and change job descriptions, or to change such positions from salaried to hourly pay status. Such changes are generally implemented only after notice is given to affected employees to our members, and to purchasers, contracted providers and vendors.
Basic Qualifications: Experience
- Minimum two (2) years of clinical nursing experience in a hospital, clinic or similar health care setting within the last three (3) years required (Bachelors degree may be substituted for one (1) year work experience).
- Minimum of a diploma from an accredited nursing school required.
- High School Diploma or General Education Development (GED) required.
- Clinical Research Professional Certificate within 12 months of hire from Society of Clinical Research Associates OR Clinical Research Associate Certificate within 12 months of hire from The Association of Clinical Research Professionals
- Registered Nurse License (California)
- Basic Life Support
- Must be proficient in electronic health systems and databases used in research environment, or willingness to learn and demonstrate proficiency within six months of hire.
- Demonstrate effective written, verbal, and interpersonal communication skills.
- Attention to detail and accuracy.
- Ability to manage multiple tasks with time deadlines.
- Demonstrate prioritization and organizational skills.
- Proficient in medical terminology.
- Demonstrate basic drug calculation skills.
- Demonstrate problem-solving skills.
- Demonstrate nursing competency skills per scope of practice (i.e., phlebotomy, performing vital signs, nursing assessments, urine dipstick reading, pregnancy test reading, performing EKG, etc.) with certification if applicable.
- Other (specific to relevant therapeutic area).
- Knowledge of GCP, federal, state, and local regulations including HIPAA and KP policies and procedures.
- Must be able to work in a Labor/Management Partnership environment.
- Clinical trials research experience preferred.
PrimaryLocation : California,San Francisco,San Francisco 4141 Geary Medical Offices,
HoursPerWeek : 40
Shift : Day
Workdays : Mon, Tue, Wed, Thu, Fri,
WorkingHoursStart : 08:30 AM
WorkingHoursEnd : 05:00 PM
Job Schedule : Full-time
Job Type : Standard
Employee Status : Regular
Employee Group/Union Affiliation : NUE-NCAL-09|NUE|Non Union Employee
Job Level : Individual Contributor
Job Category : Nursing Licensed & Nurse Practitioners
Department : Oakland Reg - 2000 Broadway - Rsrch-Invstgtr Staffg Mdl Dept - 0201
Travel : Yes, 10 % of the Time
Kaiser Permanente is an equal opportunity employer committed to a diverse and inclusive workforce. Applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), age, sexual orientation, national origin, marital status, parental status, ancestry, disability, gender identity, veteran status, genetic information, other distinguishing characteristics of diversity and inclusion, or any other protected status.
