Clinical Research Visa Sponsorship Jobs in Oregon
Oregon's clinical research sector is anchored by Oregon Health and Science University in Portland, alongside major employers like Providence Health and legacy pharma and biotech firms in the Portland metro area. International researchers and coordinators consistently find sponsorship opportunities here, particularly in academic medical centers and research-focused hospital networks across the state.
Find Clinical Research JobsOverview
Showing 5 of 63+ Clinical Research Jobs in Oregon with Visa Sponsorship
See all 63+ Clinical Research Jobs in Oregon with Visa Sponsorship
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Research Jobs in Oregon with Visa Sponsorship.
Get Access To All JobsDepartment Overview:
The Department of Emergency Medicine at OHSU is home to over 150 faculty and adjunct faculty under the direction of Mary Tanski, M.D., M.B.A., associate professor and Department Chair. Our clinician's staff at OHSU's Level 1 Trauma Center and Doernbecher Pediatric ED as well as our three community Emergency Departments (Hillsboro Medical Center, Adventist Health Portland, and Columbia Memorial Hospital), three ED Observation Units, the Immediate Care Virtual Visits Program, and the Oregon Poison Center. The Department of Emergency Medicine at OHSU has always been highly ranked in NIH Funded Research and is home to the Center for Policy and Research in Emergency Medicine (CPR-EM). Our residency program currently trains 33 residents and offers a diverse training environment through partnerships at several area hospitals. OHSU offers EM specialty training in the form of select fellowships in: Research, Education, Pediatric Emergency Medicine, Administration, EMS, Toxicology, and Ultrasound. We are proud to serve OHSU's mission of Healing, Teaching, and Discovery.
This position functions primarily as a Clinical Research Assistant supporting multiple observational, registry-based, and interventional clinical research studies within the Department of Emergency Medicine. Working closely with Principal Investigators, Research Managers, Study Coordinators, and study teams, the individual will assist with study startup, regulatory activities, participant screening and enrollment, informed consent activities, data collection and abstraction, data quality monitoring, study documentation, and study closeout activities. This person will need to be willing to conduct blood draws on subjects. Some study-related duties may involve on-call time and travel within the Portland Metro Area.
The position will coordinate research operations across multiple studies and support regulatory-compliant conduct of human subjects’ research. Responsibilities include working with electronic medical records, research databases, research participants, clinical partners, and external study collaborators while ensuring adherence to study protocols, Good Clinical Practice (GCP), HIPAA requirements, and institutional policies.
As part of professional development and workforce succession planning, this position will receive structured training in research regulatory coordination activities over time. Regulatory responsibilities will initially represent a small portion of the role and will be performed under the guidance of experienced regulatory personnel. Training will include exposure to eIRB, OnCore, protocol amendments, continuing reviews, study startup documentation, and regulatory record maintenance.
As competency develops and departmental needs evolve, regulatory responsibilities may increase. Due to the nature of emergency medicine research, this position must participate in shared after-hours and weekend study coverage to support participant enrollment and study operations when required. The ability to have a flexible schedule, day-to-day and week-to-week, is required. This person must be able to arrive at OHSU and local Portland-area hospitals within 1 hour of any study activation.
Function/Duties of Position:
- Coordinate studies. This can involve startup work, regulatory activities, study management throughout the study, screening, consenting and enrolling patients, managing data flow, coordinating documentation and data storage, coordinating prehospital and hospital data flow, reviewing timeliness and prioritization needs with the study team to facilitate adherence to study-related benchmarks.
- Review medical records, abstracting relevant variables into electronic systems. Complete enrollment forms for both registry and trial patients. Also includes Pre-Hospital and Hospital data abstraction as needed, entry, and tracking using the local and web-based study databases.
- Protocol compliance, QA/QC, study documentation - Ensure adherence to research protocol and quality of data collection. Review current protocols and policies.
- Participant, provider, and stakeholder communication - Interact with outside providers at local hospitals with ongoing study awareness, followed up by patient-level communication for consenting. Coordinate communication and meetings with external partners.
- Clinical study project coordination and study team support - Assist with assembling documentation for site progress report with PI & study team.
- Regulatory training and support activities (eIRB, OnCore, amendments, continuing reviews, regulatory files) - Assist Regulatory Coordinator with IRB and eCRIS submissions, protocol modifications; progressive training to take on additional regulatory coordinator responsibilities.
- Cover rotating after-hours call shifts for studies where 24/7 enrollment is required.
Required Qualifications:
- Bachelor's in relevant field OR
- Associate's AND 2 years of relevant experience OR
- 3 years of relevant experience OR
- Equivalent combination of training and experience
- Experience working on research studies in an emergency department.
- Work experience on at least 1 EFIC-regulated clinical trial.
- Experience obtaining informed consent from research participants.
- Experience working through at least 1 clinical trials’ full study lifecycle, from start-up to closeout, assisting in operations such as maintaining study compliance, operational efficiency, and successful study execution.
- Data collection; including the use of local and web-based databases, longitudinal data tracking, and data confidentiality rules.
- Proficient in MS, Word, Excel, and Access.
- Prior experience with any Electronic Medical Record (EMR) System.
- Ability to work with very detailed information and independent decision-making and problem-solving skills required.
- Requires exceptional attention to detail.
- Ability to multi-task and prioritize tasks/duties under pressure; outstanding interpersonal skills to interact professionally with faculty, staff, and all levels of management.
- Excellent communication skills and organizational skills.
- Ability to independently manage their daily schedule and adapt to a changing work plan.
- Able to work independently without much supervision.
- Ability to respond, as needed/assigned, after hours for study call shifts on nights and weekends.
- Must be willing to perform blood draws (phlebotomy) for studies.
- Ability to perform the job duties with or without accommodation.
Preferred Qualifications:
- Major courses in the field of research are preferred.
- Minimum 1-year experience working on research studies in an emergency department.
- Experience with data abstraction for research purposes.
- Experience supporting research regulatory submissions or maintaining regulatory study documentation.
- Familiarity with OHSU eIRB and eCRIS systems.
- Experience with study startup and closeout activities.
- Database development and management.
- Spanish language fluency Familiarity with EPIC medical record system.
- Competency with RedCap.
- Prior training in Human Subject Research, Responsible Conduct in Research and Good Clinical Practice.
- Ability to learn and apply federal, state, sponsor, and institutional regulations governing human subjects research.
- Strong document-management, organization, and records-retention skills.
- Ability to maintain accurate regulatory files and audit-ready documentation.
- SOCRA or ACRP Certification Phlebotomy Certified.
Additional Details:
Work schedule: Mon-Fri, generally during business hours (8am-6pm), start and stop times can be variable depending on work unit and study project needs. Generally, this position requires 4 days in office and can have an option for one remote workday per week. Hybrid schedules may be changed based on operational need.
Standard office setting; Daily use of computers and phones, mobile devices & study related equipment. Must be able to sit and perform repetitive computer tasks for at least 2 hours at a time. Time may be spent in the busy Emergency Department setting during clinical trial enrollments. Must be able to stand for 1-2 hours at a time during study enrollment.
Primary Work location: Marquam hill campus and telework will be primary locations. Travel to EDs, and pre-hospital agencies in the Portland-Metro area may be needed.
Occasional call shifts/ after-hours work required for study enrollment (nights/weekends, generally no more than 5-7 times/month).
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.edu.
Department Overview:
The Department of Emergency Medicine at OHSU is home to over 150 faculty and adjunct faculty under the direction of Mary Tanski, M.D., M.B.A., associate professor and Department Chair. Our clinician's staff at OHSU's Level 1 Trauma Center and Doernbecher Pediatric ED as well as our three community Emergency Departments (Hillsboro Medical Center, Adventist Health Portland, and Columbia Memorial Hospital), three ED Observation Units, the Immediate Care Virtual Visits Program, and the Oregon Poison Center. The Department of Emergency Medicine at OHSU has always been highly ranked in NIH Funded Research and is home to the Center for Policy and Research in Emergency Medicine (CPR-EM). Our residency program currently trains 33 residents and offers a diverse training environment through partnerships at several area hospitals. OHSU offers EM specialty training in the form of select fellowships in: Research, Education, Pediatric Emergency Medicine, Administration, EMS, Toxicology, and Ultrasound. We are proud to serve OHSU's mission of Healing, Teaching, and Discovery.
This position functions primarily as a Clinical Research Assistant supporting multiple observational, registry-based, and interventional clinical research studies within the Department of Emergency Medicine. Working closely with Principal Investigators, Research Managers, Study Coordinators, and study teams, the individual will assist with study startup, regulatory activities, participant screening and enrollment, informed consent activities, data collection and abstraction, data quality monitoring, study documentation, and study closeout activities. This person will need to be willing to conduct blood draws on subjects. Some study-related duties may involve on-call time and travel within the Portland Metro Area.
The position will coordinate research operations across multiple studies and support regulatory-compliant conduct of human subjects’ research. Responsibilities include working with electronic medical records, research databases, research participants, clinical partners, and external study collaborators while ensuring adherence to study protocols, Good Clinical Practice (GCP), HIPAA requirements, and institutional policies.
As part of professional development and workforce succession planning, this position will receive structured training in research regulatory coordination activities over time. Regulatory responsibilities will initially represent a small portion of the role and will be performed under the guidance of experienced regulatory personnel. Training will include exposure to eIRB, OnCore, protocol amendments, continuing reviews, study startup documentation, and regulatory record maintenance.
As competency develops and departmental needs evolve, regulatory responsibilities may increase. Due to the nature of emergency medicine research, this position must participate in shared after-hours and weekend study coverage to support participant enrollment and study operations when required. The ability to have a flexible schedule, day-to-day and week-to-week, is required. This person must be able to arrive at OHSU and local Portland-area hospitals within 1 hour of any study activation.
Function/Duties of Position:
- Coordinate studies. This can involve startup work, regulatory activities, study management throughout the study, screening, consenting and enrolling patients, managing data flow, coordinating documentation and data storage, coordinating prehospital and hospital data flow, reviewing timeliness and prioritization needs with the study team to facilitate adherence to study-related benchmarks.
- Review medical records, abstracting relevant variables into electronic systems. Complete enrollment forms for both registry and trial patients. Also includes Pre-Hospital and Hospital data abstraction as needed, entry, and tracking using the local and web-based study databases.
- Protocol compliance, QA/QC, study documentation - Ensure adherence to research protocol and quality of data collection. Review current protocols and policies.
- Participant, provider, and stakeholder communication - Interact with outside providers at local hospitals with ongoing study awareness, followed up by patient-level communication for consenting. Coordinate communication and meetings with external partners.
- Clinical study project coordination and study team support - Assist with assembling documentation for site progress report with PI & study team.
- Regulatory training and support activities (eIRB, OnCore, amendments, continuing reviews, regulatory files) - Assist Regulatory Coordinator with IRB and eCRIS submissions, protocol modifications; progressive training to take on additional regulatory coordinator responsibilities.
- Cover rotating after-hours call shifts for studies where 24/7 enrollment is required.
Required Qualifications:
- Bachelor's in relevant field OR
- Associate's AND 2 years of relevant experience OR
- 3 years of relevant experience OR
- Equivalent combination of training and experience
- Experience working on research studies in an emergency department.
- Work experience on at least 1 EFIC-regulated clinical trial.
- Experience obtaining informed consent from research participants.
- Experience working through at least 1 clinical trials’ full study lifecycle, from start-up to closeout, assisting in operations such as maintaining study compliance, operational efficiency, and successful study execution.
- Data collection; including the use of local and web-based databases, longitudinal data tracking, and data confidentiality rules.
- Proficient in MS, Word, Excel, and Access.
- Prior experience with any Electronic Medical Record (EMR) System.
- Ability to work with very detailed information and independent decision-making and problem-solving skills required.
- Requires exceptional attention to detail.
- Ability to multi-task and prioritize tasks/duties under pressure; outstanding interpersonal skills to interact professionally with faculty, staff, and all levels of management.
- Excellent communication skills and organizational skills.
- Ability to independently manage their daily schedule and adapt to a changing work plan.
- Able to work independently without much supervision.
- Ability to respond, as needed/assigned, after hours for study call shifts on nights and weekends.
- Must be willing to perform blood draws (phlebotomy) for studies.
- Ability to perform the job duties with or without accommodation.
Preferred Qualifications:
- Major courses in the field of research are preferred.
- Minimum 1-year experience working on research studies in an emergency department.
- Experience with data abstraction for research purposes.
- Experience supporting research regulatory submissions or maintaining regulatory study documentation.
- Familiarity with OHSU eIRB and eCRIS systems.
- Experience with study startup and closeout activities.
- Database development and management.
- Spanish language fluency Familiarity with EPIC medical record system.
- Competency with RedCap.
- Prior training in Human Subject Research, Responsible Conduct in Research and Good Clinical Practice.
- Ability to learn and apply federal, state, sponsor, and institutional regulations governing human subjects research.
- Strong document-management, organization, and records-retention skills.
- Ability to maintain accurate regulatory files and audit-ready documentation.
- SOCRA or ACRP Certification Phlebotomy Certified.
Additional Details:
Work schedule: Mon-Fri, generally during business hours (8am-6pm), start and stop times can be variable depending on work unit and study project needs. Generally, this position requires 4 days in office and can have an option for one remote workday per week. Hybrid schedules may be changed based on operational need.
Standard office setting; Daily use of computers and phones, mobile devices & study related equipment. Must be able to sit and perform repetitive computer tasks for at least 2 hours at a time. Time may be spent in the busy Emergency Department setting during clinical trial enrollments. Must be able to stand for 1-2 hours at a time during study enrollment.
Primary Work location: Marquam hill campus and telework will be primary locations. Travel to EDs, and pre-hospital agencies in the Portland-Metro area may be needed.
Occasional call shifts/ after-hours work required for study enrollment (nights/weekends, generally no more than 5-7 times/month).
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.edu.
Clinical Research Job Roles in Oregon
See all 63+ Clinical Research Jobs in Oregon
Sign up for free to filter by visa type, set job alerts, and find employers with verified sponsorship history.
Search Clinical Research Jobs in OregonClinical Research Jobs in Oregon: Frequently Asked Questions
Which companies sponsor visas for clinical research professionals in Oregon?
Oregon Health and Science University is one of the most active sponsors for clinical research roles in the state, given its size and volume of active trials. Providence Health and Services, Legacy Health, and smaller contract research organizations operating in the Portland metro area have also filed H-1B visa petitions for clinical research positions. Academic medical centers tend to have dedicated HR infrastructure for sponsorship, which makes the process more predictable than smaller employers.
Which visa types are most common for clinical research roles in Oregon?
The H-1B is the most common visa category for clinical research coordinators, research scientists, and biostatisticians in Oregon, as these roles typically require a bachelor's degree or higher in a specific field and qualify as specialty occupations. J-1 visas are also used at academic institutions like OHSU for research scholars and postdoctoral fellows. Candidates with advanced degrees may also explore the EB-2 NIW pathway, though that involves a longer permanent residency process.
Which cities in Oregon have the most clinical research sponsorship jobs?
Portland is by far the dominant market for clinical research visa sponsorship in Oregon. OHSU's South Waterfront campus and its affiliated research programs generate the largest concentration of openings. The broader Portland metro, including Beaverton and Hillsboro, also has activity tied to health system research arms and some biotech presence. Eugene has limited but occasional opportunities through PeaceHealth and University of Oregon-affiliated programs.
How to find clinical research visa sponsorship jobs in Oregon?
Migrate Mate filters job listings specifically by visa sponsorship availability, which removes the guesswork of sorting through postings that won't support international candidates. For clinical research roles in Oregon, you can search by role type and state to surface positions at institutions like OHSU, Providence, and regional CROs that have a history of sponsoring. Migrate Mate's focus on sponsorship-confirmed jobs makes it more efficient than general job searches for this purpose.
Are there any Oregon-specific considerations for clinical research visa sponsorship candidates?
Oregon's clinical research hiring is concentrated in academic and nonprofit health systems, which are cap-exempt for H-1B purposes. This means institutions like OHSU can file H-1B petitions at any time of year without being subject to the annual lottery, which is a meaningful advantage for international candidates. Prevailing wage requirements still apply and are set based on the Portland-Vancouver-Hillsboro metropolitan area wage data, so job offers must meet Department of Labor benchmarks for the specific role and location.
What is the prevailing wage for sponsored clinical research jobs in Oregon?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.