Palo Alto Veterans Institute for Research
Clinical Research Nurse - TMS
Palo Alto Veterans Institute for Research, Palo Alto, California, United States, 94306
Palo Alto Veterans Institute for Research (PAVIR) supports the nation's second largest research program conducted among the VA Hospitals and is looking for a full-time Clinical Research Nurse - TMS. The position is for a nurse practitioner researcher for a VA cooperative clinical study in the division of Psychiatry. The study evaluates the effectiveness of repetitive transcranial magnetic stimulation (rTMS) as a treatment for Treatment Resistant Major Depression (TRMD). The researcher is expected to provide experimental treatment to veterans at the VA Palo Alto Health Care System. Palo Alto is one of the 9 VA Medical Centers participating in the study.
BENEFITS
PAVIR offers generous benefits, including comprehensive health insurance, vision, dental, 14 paid holidays, paid vacation time, sick pay, a 401(k) with a fully vested 6% company match and 3% profit share, a wellness program, commuter benefits, and professional development training. Plus, we pay for life, short-term disability, and long-term disability insurance.
JOB RESPONSIBILITIES
Responsible to the local Site Investigator of the research trial;Works directly with site investigator(s), study coordinator and other facility staff. Responsible for assisting in the initiation of new studies, including submission of required regulatory documents to IRB and R and D committees and subcommittees, initiation visits by study sponsor, preparation of informed consent, data collection and evaluation and recruitment of potential study participants;Oversees the day-to-day activities of the project and acts as the resource person for all questions about the study activities locally;Maintains a high level of knowledge and understanding of the study protocol, including all requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information and device accountability requirements.Assisting in the selection, contacting and scheduling potential research subjects;Assisting in the assessment of inclusion and exclusion criteria for each potential patient;Coordinate and conduct patient care visits and assure all procedures are conducted in compliance with the study protocol;Responsible for maintaining close contact and ongoing supportive relationship with study patients during treatment and follow-up phases, including weekly (during the acute treatment phase) and monthly follow-up assessments and interviews (during the follow-up phase);Administer structured assessments, and conduct audiometric testing;Obtain motor threshold determination and administer rTMS treatments according to the study protocol. Provides education and instruction on rTMS treatment and possible adverse effects.Perform venipunctures for collection of blood samples required by study protocol, including processing of samples and proper shipment per regulatory guidelines;Collects and maintains accurate source documentation for each study participant. Accurately documents in CPRS, completes data entry and responds to sponsor queries; initiates physician orders and creates source documents. Maintains regulatory documents and sponsor files;Assures confidentiality and security of human participants and data collected in accordance with HIPAA regulations. Adheres to Federal Privacy regulations;Acts to protect the rights, safety and well being of human participants involved in clinical trials. Complies with ethical standards for research conduct.Requires knowledge of good clinical practices as well as the ability to work independently;Fosters collaborative research relationships using excellent communication and interpersonal skills with investigators and participants;Interact with Site Investigator as needed to ensure patients receive appropriate medical and psychiatric evaluation and care when needed;and alerts Site Investigator of adver e events when appropriate.Other tasks as assigned.
QUALIFICATIONS
Required: Graduate of a school of professional nursing or medical school;Valid Driver License required;RN license required;1 year or more of nursing experience.Preferred: Approved by the appropriate State-accrediting agency;Previous experience in a clinical and research environment;Experience with grants and contracts function, clinical trial and research data management;Good understanding of clinical terminology and procedures gained through experience;Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices;Ability to read and understand study/trial protocol;Ability to prioritize and organize a high-volume workload and adapt to changing priorities;Demonstrated ability to work independently and cooperatively;Demonstrated ability to work and communicate effectively with study subjects;Proven track record towards meeting goals and deadlines;Strong interpersonal skills;Proficiency with Microsoft Office and database applications is preferred.Knowledge of VA and its health care system regarding clinical research trials and understanding of VA procedures and safety regulations is strongly desired;Some clinical device experience is preferred;Knowledge of and experience working in orthopedic research is desired;Knowledge of medical terminology is strongly preferred.
ABOUT PALO ALTO VETERANS INSTITUTE FOR RESEARCH (PAVIR)
PAVIR facilitates research and education activities conducted at the VA Palo Alto Health Care System. At PAVIR we work with more than 160 uniquely talented medical scientists. We recruit and retain talented employees who believe in making a difference in the lives of others through innovative health research.
READY TO JOIN OUR RESEARCH TEAM?
If you feel that you would be right for this job, please fill out our initial 3-minute, mobile-friendly application. We look forward to meeting you!
PAVIR is a nonprofit foundation affiliated with the Veterans Affairs Palo Alto Health Care System (VAPAHCS). As a condition of employment, all PAVIR employees are required to have an approved appointment with VAPAHCS and complete a background check before they can commence work.
PAVIR is pleased to be an Equal Opportunity Employer. Minorities, Women, Veterans, and Individuals with a Disability are encouraged to apply. We welcome and encourage diversity in the workplace regardless of race, color, religion, age, gender, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law. If you need special assistance or an accommodation to apply for a posted position, please contact jobs@pavir.org - Human Resources department.
For more information, or to apply now, you must go to the website below. Please DO NOT email your resume to us as we only accept applications through our website.
BENEFITS
PAVIR offers generous benefits, including comprehensive health insurance, vision, dental, 14 paid holidays, paid vacation time, sick pay, a 401(k) with a fully vested 6% company match and 3% profit share, a wellness program, commuter benefits, and professional development training. Plus, we pay for life, short-term disability, and long-term disability insurance.
JOB RESPONSIBILITIES
Responsible to the local Site Investigator of the research trial;Works directly with site investigator(s), study coordinator and other facility staff. Responsible for assisting in the initiation of new studies, including submission of required regulatory documents to IRB and R and D committees and subcommittees, initiation visits by study sponsor, preparation of informed consent, data collection and evaluation and recruitment of potential study participants;Oversees the day-to-day activities of the project and acts as the resource person for all questions about the study activities locally;Maintains a high level of knowledge and understanding of the study protocol, including all requirements for patient visits, obtaining informed consent, patient visit schedules, test procedures, laboratory information and device accountability requirements.Assisting in the selection, contacting and scheduling potential research subjects;Assisting in the assessment of inclusion and exclusion criteria for each potential patient;Coordinate and conduct patient care visits and assure all procedures are conducted in compliance with the study protocol;Responsible for maintaining close contact and ongoing supportive relationship with study patients during treatment and follow-up phases, including weekly (during the acute treatment phase) and monthly follow-up assessments and interviews (during the follow-up phase);Administer structured assessments, and conduct audiometric testing;Obtain motor threshold determination and administer rTMS treatments according to the study protocol. Provides education and instruction on rTMS treatment and possible adverse effects.Perform venipunctures for collection of blood samples required by study protocol, including processing of samples and proper shipment per regulatory guidelines;Collects and maintains accurate source documentation for each study participant. Accurately documents in CPRS, completes data entry and responds to sponsor queries; initiates physician orders and creates source documents. Maintains regulatory documents and sponsor files;Assures confidentiality and security of human participants and data collected in accordance with HIPAA regulations. Adheres to Federal Privacy regulations;Acts to protect the rights, safety and well being of human participants involved in clinical trials. Complies with ethical standards for research conduct.Requires knowledge of good clinical practices as well as the ability to work independently;Fosters collaborative research relationships using excellent communication and interpersonal skills with investigators and participants;Interact with Site Investigator as needed to ensure patients receive appropriate medical and psychiatric evaluation and care when needed;and alerts Site Investigator of adver e events when appropriate.Other tasks as assigned.
QUALIFICATIONS
Required: Graduate of a school of professional nursing or medical school;Valid Driver License required;RN license required;1 year or more of nursing experience.Preferred: Approved by the appropriate State-accrediting agency;Previous experience in a clinical and research environment;Experience with grants and contracts function, clinical trial and research data management;Good understanding of clinical terminology and procedures gained through experience;Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices;Ability to read and understand study/trial protocol;Ability to prioritize and organize a high-volume workload and adapt to changing priorities;Demonstrated ability to work independently and cooperatively;Demonstrated ability to work and communicate effectively with study subjects;Proven track record towards meeting goals and deadlines;Strong interpersonal skills;Proficiency with Microsoft Office and database applications is preferred.Knowledge of VA and its health care system regarding clinical research trials and understanding of VA procedures and safety regulations is strongly desired;Some clinical device experience is preferred;Knowledge of and experience working in orthopedic research is desired;Knowledge of medical terminology is strongly preferred.
ABOUT PALO ALTO VETERANS INSTITUTE FOR RESEARCH (PAVIR)
PAVIR facilitates research and education activities conducted at the VA Palo Alto Health Care System. At PAVIR we work with more than 160 uniquely talented medical scientists. We recruit and retain talented employees who believe in making a difference in the lives of others through innovative health research.
READY TO JOIN OUR RESEARCH TEAM?
If you feel that you would be right for this job, please fill out our initial 3-minute, mobile-friendly application. We look forward to meeting you!
PAVIR is a nonprofit foundation affiliated with the Veterans Affairs Palo Alto Health Care System (VAPAHCS). As a condition of employment, all PAVIR employees are required to have an approved appointment with VAPAHCS and complete a background check before they can commence work.
PAVIR is pleased to be an Equal Opportunity Employer. Minorities, Women, Veterans, and Individuals with a Disability are encouraged to apply. We welcome and encourage diversity in the workplace regardless of race, color, religion, age, gender, sexual orientation, national origin, disability status, protected veteran status, or any other characteristic protected by law. If you need special assistance or an accommodation to apply for a posted position, please contact jobs@pavir.org - Human Resources department.
For more information, or to apply now, you must go to the website below. Please DO NOT email your resume to us as we only accept applications through our website.