Contributing to manuscripts, grants, presentations, and IRB records. * Other duties as assigned ... one weekend per month, as required to support human participant research protocols. * Clinical ...
Contributing to manuscripts, grants, presentations, and IRB records. * Other duties as assigned ... one weekend per month, as required to support human participant research protocols. * Clinical ...
Clinical Research Assistant
Portland, OR · On-site
Contributing to manuscripts, grants, presentations, and IRB records. * Other duties as assigned ... one weekend per month, as required to support human participant research protocols. * Clinical ...
Clinical Research Assistant
Portland, OR · On-site
Contributing to manuscripts, grants, presentations, and IRB records. * Other duties as assigned ... one weekend per month, as required to support human participant research protocols. * Clinical ...
Contributing to manuscripts, grants, presentations, and IRB records. * Other duties as assigned ... one weekend per month, as required to support human participant research protocols. * Clinical ...
Contributing to manuscripts, grants, presentations, and IRB records. * Other duties as assigned ... one weekend per month, as required to support human participant research protocols. * Clinical ...
Clinical Research Assistant
Portland, OR · On-site
$23.18 - $33.02/hr
Contributing to manuscripts, grants, presentations, and IRB records. * Other duties as assigned ... one weekend per month, as required to support human participant research protocols. * Clinical ...
Clinical Research Assistant
Portland, OR · On-site
$23.18 - $33.02/hr
Contributing to manuscripts, grants, presentations, and IRB records. * Other duties as assigned ... one weekend per month, as required to support human participant research protocols. * Clinical ...
Clinical Research Assistant
Portland, OR · On-site
Contributing to manuscripts, grants, presentations, and IRB records. * Other duties as assigned ... one weekend per month, as required to support human participant research protocols. * Clinical ...
Clinical Research Assistant
Portland, OR · On-site
Contributing to manuscripts, grants, presentations, and IRB records. * Other duties as assigned ... one weekend per month, as required to support human participant research protocols. * Clinical ...
Neuroanesthesia Fellow
$52K - $70K/yr
Elective surgical schedule Monday - Friday and fair share of nights, holidays and weekends. In ... IRB, NIH and all other state, federal, and institutional regulatory guidelines). Treats all ...
Neuroanesthesia Fellow
$52K - $70K/yr
Elective surgical schedule Monday - Friday and fair share of nights, holidays and weekends. In ... IRB, NIH and all other state, federal, and institutional regulatory guidelines). Treats all ...
Neuroanesthesia Fellow
$52K - $70K/yr
Elective surgical schedule Monday - Friday and fair share of nights, holidays and weekends. In ... IRB, NIH and all other state, federal, and institutional regulatory guidelines). Treats all ...
Neuroanesthesia Fellow
$52K - $70K/yr
Elective surgical schedule Monday - Friday and fair share of nights, holidays and weekends. In ... IRB, NIH and all other state, federal, and institutional regulatory guidelines). Treats all ...
Neuroanesthesia Fellow
Portland, OR · On-site
$52K - $70K/yr
Elective surgical schedule Monday - Friday and fair share of nights, holidays and weekends. In ... IRB, NIH and all other state, federal, and institutional regulatory guidelines). Treats all ...
Neuroanesthesia Fellow
Portland, OR · On-site
$52K - $70K/yr
Elective surgical schedule Monday - Friday and fair share of nights, holidays and weekends. In ... IRB, NIH and all other state, federal, and institutional regulatory guidelines). Treats all ...
Neuroanesthesia Fellow
Portland, OR · On-site
$52K - $70K/yr
Elective surgical schedule Monday - Friday and fair share of nights, holidays and weekends. In ... IRB, NIH and all other state, federal, and institutional regulatory guidelines). Treats all ...
Neuroanesthesia Fellow
Portland, OR · On-site
$52K - $70K/yr
Elective surgical schedule Monday - Friday and fair share of nights, holidays and weekends. In ... IRB, NIH and all other state, federal, and institutional regulatory guidelines). Treats all ...
Neuroanesthesia Fellow
Portland, OR · On-site
$52K - $70K/yr
Elective surgical schedule Monday - Friday and fair share of nights, holidays and weekends. In ... IRB, NIH and all other state, federal, and institutional regulatory guidelines). Treats all ...
Neuroanesthesia Fellow
Portland, OR · On-site
$52K - $70K/yr
Elective surgical schedule Monday - Friday and fair share of nights, holidays and weekends. In ... IRB, NIH and all other state, federal, and institutional regulatory guidelines). Treats all ...
Neuroanesthesia Fellow
$52K - $70K/yr
Elective surgical schedule Monday - Friday and fair share of nights, holidays and weekends. In ... IRB, NIH and all other state, federal, and institutional regulatory guidelines). Treats all ...
Neuroanesthesia Fellow
$52K - $70K/yr
Elective surgical schedule Monday - Friday and fair share of nights, holidays and weekends. In ... IRB, NIH and all other state, federal, and institutional regulatory guidelines). Treats all ...
Clinical Research Coordinator I, II, or III
Portland, OR · On-site
$25.75 - $34.25/hr
Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs * Manage subject recruitment, informed consent, and retention strategies * Ensure timely ...
Clinical Research Coordinator I, II, or III
Portland, OR · On-site
$25.75 - $34.25/hr
Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs * Manage subject recruitment, informed consent, and retention strategies * Ensure timely ...
Senior Clinical Research Coordinator
Portland, OR · On-site
$25.75 - $34.25/hr
Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs * Manage subject recruitment, informed consent, and retention activities * Ensure timely EDC data ...
Senior Clinical Research Coordinator
Portland, OR · On-site
$25.75 - $34.25/hr
Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs * Manage subject recruitment, informed consent, and retention activities * Ensure timely EDC data ...
Senior Clinical Research Coordinator
Portland, OR · On-site
$25.75 - $34.25/hr
Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs * Manage subject recruitment, informed consent, and retention activities * Ensure timely EDC data ...
Senior Clinical Research Coordinator
Portland, OR · On-site
$25.75 - $34.25/hr
Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs * Manage subject recruitment, informed consent, and retention activities * Ensure timely EDC data ...
TI Sr Clinical Research Assistant (Clinical Research Coordinator)
Portland, OR · On-site
$25.75 - $34.25/hr
Working with the regulatory management team to complete all regulatory documentation in accordance with their role as required by the OHSU IRB and sponsor * Creation of study trackers and ...
TI Sr Clinical Research Assistant (Clinical Research Coordinator)
Portland, OR · On-site
$25.75 - $34.25/hr
Working with the regulatory management team to complete all regulatory documentation in accordance with their role as required by the OHSU IRB and sponsor * Creation of study trackers and ...
Working with the regulatory management team to complete all regulatory documentation in accordance with their role as required by the OHSU IRB and sponsor * Creation of study trackers and ...
Working with the regulatory management team to complete all regulatory documentation in accordance with their role as required by the OHSU IRB and sponsor * Creation of study trackers and ...
TI Sr Clinical Research Assistant (Clinical Research Coordinator)
Portland, OR · On-site
$50K - $84K/yr
Working with the regulatory management team to complete all regulatory documentation in accordance with their role as required by the OHSU IRB and sponsor * Creation of study trackers and ...
TI Sr Clinical Research Assistant (Clinical Research Coordinator)
Portland, OR · On-site
$50K - $84K/yr
Working with the regulatory management team to complete all regulatory documentation in accordance with their role as required by the OHSU IRB and sponsor * Creation of study trackers and ...
Clinical Research Coordinator I, II, or III
Portland, OR · On-site
$25.75 - $34.25/hr
Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs * Manage subject recruitment, informed consent, and retention strategies * Ensure timely ...
Clinical Research Coordinator I, II, or III
Portland, OR · On-site
$25.75 - $34.25/hr
Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs * Manage subject recruitment, informed consent, and retention strategies * Ensure timely ...
Working with the regulatory management team to complete all regulatory documentation in accordance with their role as required by the OHSU IRB and sponsor * Creation of study trackers and ...
Working with the regulatory management team to complete all regulatory documentation in accordance with their role as required by the OHSU IRB and sponsor * Creation of study trackers and ...
Weekend Irb information
What is the difference between Weekend IRB vs IRB Coordinator?
| Aspect | Weekend IRB | IRB Coordinator |
|---|---|---|
| Certifications | Often requires IRB-related training, but not always formal certifications | Typically requires IRB or research compliance certifications |
| Work Environment | Part-time, flexible hours, often on weekends or evenings | Full-time, office-based, regular weekday schedule |
| Employer & Industry | Research institutions, hospitals, universities | Research institutions, hospitals, universities |
Weekend IRB roles focus on providing oversight during non-standard hours, often with flexible schedules, while IRB Coordinators handle ongoing compliance, documentation, and communication during regular hours. Both roles are essential in research oversight but differ mainly in work hours and specific responsibilities.
What is a weekend IRB?
What are the typical responsibilities of a weekend IRB member?
What are the key skills and qualifications needed to thrive as a weekend IRB member?
Oregon Health & Science University rating
8.1
Based on 95 frontline employees who took The Breakroom Quiz
154th of 614 rated colleges and universities
Job description
The Oregon Institute of Occupational Health Sciences is an independent research institute within OHSU that is dedicated to health and safety in the workplace. The Institute receives its base funding from the Oregon Workers' Compensation Fund and leverages this base funding to secure federal government grants in basic, clinical, and applied research. We perform biomedical/occupational research and innovation for a healthy workforce, aimed at promoting health and reducing disease and disability among workers across the nation, particularly in Oregon.
The Clinical Physiology and Chronobiology Program (CPCP) within the Institute specializes in clinical research on the effects of sleep and circadian rhythms on physiology and pathophysiology in humans.
The clinical research assistant will work on various projects under the direction of Dr. Nicole Bowles (PI), Assistant Professor within the Oregon Institute of Occupational Health Sciences, and may also be supervised by postdoctoral fellows or senior research staff.
Function/Duties of PositionThis position works on research aimed at understanding the effects of changes to the environment and behaviors on sleep and circadian rhythms and the subsequent impact on physiology and pathophysiology in humans. Specifically, this research is investigating the adverse health effects of shift work including the body's response to stressors at night, the use of cannabis and related projects as sleep aids, and how sleep and circadian rhythms may contribute to racial disparities in health. These studies will lead to interventions designed to improve the health, safety and well-being of night shift workers and vulnerable populations.
- Medically screening volunteer research participants over the phone and in person and collecting data using a variety of noninvasive physiological monitoring devices (e.g.,EKG, blood pressure, breathing, sleep, core body temperature).
- Managing and analyzing data to address research hypotheses.
- Developing recruitment materials (e.g., online and print advertisements and surveys) and traveling locally to place flyers/advertisements in public locations to attract study participants.
- Setting up, testing, and maintaining equipment.
- Contributing to manuscripts, grants, presentations, and IRB records.
- Other duties as assigned.
- Bachelor's degree in relevant field; OR
- Associates degree AND 2 years relevant experience; OR
- 3 years relevant experience; OR
- Equivalent combination of training & experience.
Skills and Abilities
- Ability to work a flexible schedule that includes up to six overnight laboratory sessions per month and approximately one weekend per month, as required to support human participant research protocols.
- Clinical research, especially related to human-subjects research.
- Experience with circadian rhythm or sleep research.
- Experience with polysomnography setup, signal acquisition, and overnight monitoring.
- Experience reviewing PSG recordings for signal quality, scoring readiness, and identification of recording artifacts.
- Experience with continuous beat-to-beat blood pressure monitoring (e.g., Finapres or CNAP systems) and physiological signal quality assurance.
- Experience collecting and processing electrodermal activity (galvanic skin response), ECG/heart rate variability, and other autonomic physiology measures.
- Experience collecting, processing, and quality-controlling complex physiological data from human laboratory studies, including sleep, cardiovascular, autonomic, and circadianmeasures.
- Proficiency with Microsoft Office, including advanced Microsoft Excel skills (e.g., data entry, formula creation, filtering/sorting, data validation, and management of research datasets), Microsoft Word, Outlook, and PowerPoint.
- Experience using REDCap for participant data entry, longitudinal study management, and survey administration.
- Experience maintaining equipment calibration and troubleshooting physiological recording systems.
- Demonstrated ability to independently coordinate multiple concurrent research studies, prioritize competing deadlines, maintain accurate study documentation, and ensure timely completion of research activities while adhering to study protocols.
- Demonstrated ability to communicate professionally, accurately, and in a timely manner with research participants, investigators, clinical collaborators, and regulatory personnel through written, verbal, and electronic communication.
- Commitment to maintaining participant confidentiality, data security, and adherence to human subjects research regulations (HIPAA and IRB requirements, as applicable).
- Demonstrated ability to identify, compile, organize, and summarize scientific literature, study documentation, and research-related information from published literature, institutional resources, and external collaborators.
- Bachelor's degree in a biological-science field.
- Specialized experience with computer programing and/or digital media.
- Experience designing or modifying REDCap projects, including development of longitudinal surveys, branching logic, calculated fields, and automated workflows.
- Demonstrated ability to work both independently and collaboratively within a multidisciplinary research team, while maintaining productive and professional interactions with investigators, staff, trainees, and research participants from diverse backgrounds.
- Experience recruiting and retaining research participants with varying patterns of cannabis/cannabinoid use for human-subjects research studies.
Requires ongoing on-site work and travel. Some teleworking may be negotiated. This position will regularly include evening, overnight, and weekend shifts, as well as interacting with research participants.
Why apply to OHSU?We are Oregon's only public academic health center. In addition to caring for patients, we lead groundbreaking research. We also train the next generation of health care professionals. As Portland's largest employer, we give you opportunities to learn and advance in a system of hospitals and clinics across Oregon and Southwest Washington. All are welcome. OHSU welcomes people of all ages, ethnicities, genders, national origins, religions and sexual orientations. We are striving to build an anti-racist, multicultural institution and encourage people with diverse backgrounds to apply. To request reasonable accommodation, contact askhr@ohsu.eduEmployment Type: OTHERWhat Oregon Health & Science University employees say
Pay
Benefits
Hours and flexibility
Workplace
Get the full story on Breakroom
About Oregon Health & Science University
Sourced by ZipRecruiter
Oregon Health & Science University (OHSU) is a distinguished institution under the industry of higher education and healthcare, specifically in the field of medical science. Based in Portland, Oregon, US, it maintains a reputation for promoting research, teaching, patient care, and outreach. Established in 1887, OHSU has continually sought to redefine the parameters of healthcare delivery and biomedical discovery through its expansive catalog of programs and initiatives. A galvanizing mission drives OHSU: to improve the health and quality of life for all Oregonians through excellence, innovation, and leadership in health care, education, and research.
Industry
Colleges, universities, and professional schools
Company size
10,000+ Employees
Headquarters location
Portland, OR, US
Year founded
1887