J-1 Visa Clinical Analyst Jobs
Clinical Analyst roles in the United States are typically available to exchange visitors through the J-1 visa Trainee or Research Scholar program category, depending on your career stage and host organization. A designated sponsor issues your DS-2019 and arranges sponsorship, while the hiring employer serves as your host site.
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The mission of the Knight Cancer Clinical Research organization is to support the conduct of translational clinical research aimed at improving the lives of people and families with cancer by applying innovative strategies for cancer prevention, screening, diagnosis and treatment. The support is provided through proactive, high quality and efficient study management in compliance with federal regulations and local policies and procedures. This fast-paced and intense research environment requires complex clinical research studies involving a very vulnerable and sick population.
Position Summary:
This TI Clinical Research Associate will be known internally as a Float Clinical Research Associate (Float CRA). It is a collaborative role supporting clinical research programs of the Knight Cancer Clinical Research organization. The Float CRA will support the conduct of translational clinical research aimed at improving the lives of people and families with cancer by applying innovative strategies for cancer prevention, screening, diagnosis, and treatment. The support is provided through proactive, high quality, and efficient study management in compliance with federal regulations and local policies and procedures. This fast-paced and intense research environment requires management of complex clinical research studies involving a vulnerable patient population.
The position will work with different programs within the Knight Cancer Clinical Research operation. They will provide relief, backup, or interim support to maintain progress on critical projects when there are staffing transitions or increased volume. Under occasional supervision, the Float CRA will perform a broad variety of tasks necessary for implementation and overall management of complex therapeutic interventional clinical research. Specific tasks and roles will be determined by the needs of the clinical research program with which the Float CRA is engaged.
These responsibilities will include the coordination of all aspects of a study as specifically outlined in the protocol. Primary focus will be patient safety and compliance with the prescribed protocol and Good Clinical Practice. The Float CRA will work collaboratively with physician, nursing, and ancillary staff in the scheduling and management of subject research activities. The Float CRA will maintain accurate, complete, and timely records on all research subjects including preparation of source documentation and clinical research data/case report forms. The Float CRA may have direct patient contact, process biological samples and may perform other non-invasive testing such as ECGs.
The Float CRA may represent the investigator and institution during monitor visits and on-site audits conducted by the sponsor or sponsor representative. The successful Float CRA will have and maintain a working knowledge of National Cancer Institute (NCI), FDA, DHHS and other agency guidelines that govern clinical research.
Given the complexities of oncology research and the challenges of working with a terminally ill population, strong customer service, organizational, and interpersonal skills are required. The ability to clearly organize and/or adapt to multiple priorities and deadlines at one time is necessary. Attention to detail, service orientation, delegation and project management skills, and above average critical judgment skills are essential. Therapeutic Interventional trials are treatment studies that involve people who have a disease or underlying condition. They include the administration and testing new treatments or new ways of using existing treatments, such as new drugs, vaccines, cell therapies, devices, experimental approaches to surgery or radiation therapy, etc.
OHSU Research classification: TI Clinical Research Associate, represented by the Research Workers United (RWU), subject to the active collective bargaining agreement between OHSU and RWU.
Duties & Responsibilities:
Study Coordination
Responsible for coordinating aspects of oncology clinical trials from startup to closeout and assuring conduct of trials in accordance with NCI and FDA guidelines. This includes but is not limited to:
- Communicate effectively across multiple clinical teams for clinical trial coordination.
- Be able to navigate and understand complex oncology clinical trial protocols.
- Explain trial logistics to oncology patients, triage and ensure all patient questions are answered.
- Assist the PI or Sub-I with the informed consent process.
- Assist the PI or Sub-I with the collection and documentation of subject adverse events.
- Document study required source documentation in the subjects’ medical record or paper source.
- Communicate with the PI or Sub-I during patient visits regarding dose modification parameters.
- Serve as the point of contact for the clinical staff to provide protocol guidance for patient management on trial.
- Triage research patient communications to the personnel most appropriately trained to address their questions/needs.
- Place research lab and procedure orders in compliance with the approved billing schedule.
- Review patient records to screen for potential trials.
- Remove barriers for patients to participate in clinical trials. This may include working with their PCP or local oncologist to get procedures done close to home, connecting them to social work to find travel and financial resources, setting up virtual medicine visits, or referring to another useful resource.
- Perform and document drug accountability.
- Prepare for upcoming visits including reviewing patient records to look for newly reported adverse events, concomitant medications, and other pertinent information to be reviewed with the patient and provider at the visit.
- Submit insurance pre-authorization request for new patients on study.
- Schedule research biopsies, scans, ECHOs/ECGs, Ophthalmology appointments, dermatology visits and other research required procedures as needed.
- Provide clinic training in-services as needed.
- Review patient records to determine eligibility for enrollment into clinical trials. Confirm with the investigator that subject meets appropriate inclusion criteria for clinical trial.
- Communicate all pre-treatment requirements to investigator/clinical staff.
- Obtain and submit imaging studies, pathology, or other samples as required by protocol.
- Verify that procedures/services are billed in accordance with the approved billing schedule.
- Submit Invoices for tasks related to their role.
- Review and report adverse events or Unanticipated Problems to IRB and the study sponsor.
- Obtain vital signs and/or ECG measurements for study patients; conduct protocol-required tests such as the sit-to-stand test or walk test documenting contacts with study subjects as appropriate.
- Procure, process, and ship human biological specimens (including but not limited to blood, urine, feces, sputum, tissue) in adherence with protocol parameters and appropriate training.
- Communicate and facilitate oncology trial guidelines, timelines, and patient specifics with Research Pharmacy, Clinics and various service departments to coordinate treatment for the study patient.
- Ensure compliance with FDA and regulatory reporting agencies.
- Report any non-compliance to study investigator / departmental staff.
- Prepare any necessary materials for required internal and external (sponsor, FDA) regulatory and quality control audits and sponsor monitoring visits.
- May assist and collaborate with principal investigator and sub-principal investigators in clinic during patient appointments, consenting appointments and treatment appointments to ensure protocol is being adhered to and proper documentation is recorded.
Data Management
- Collection and entry of oncology data from patient medical records into study databases.
- Internal tracking and reporting.
- Obtaining and uploading imaging.
- Collaborate with study team to resolve data queries within deadlines.
- Work with study team to correct any quality control issues.
- Collaborate with study representatives to maintain data integrity.
- Lab grading.
- Obtaining study team signatures.
- Scheduling and conducting study monitoring visits.
- Collaborate with the study team to resolve any oncology data queries identified by the study monitor, auditor, or other individual reviewing the study data within tight deadlines with competing priorities.
- Work with the study team to correct any quality control issues with the data entry.
Education and Process Improvement
- Participate in continuing education activities to maintain current knowledge of oncology, research regulatory requirements, and process improvements for clinical trials.
- May assist with or lead training of junior team members.
- May assist or take lead in developing standard procedures for collaboration with clinic operations, sponsor representatives, and across CRM programs.
Audit preparation
- May assist with preparation activities for audit or inspection.
- May perform ad hoc internal monitoring.
Required Qualifications:
Education & Experience:
- Master's Degree in relevant field AND 3 years of clinical research coordination experience OR
- Bachelor's Degree in relevant field AND 5 years of clinical research coordination experience.
- SoCRA or ACRP required within 12 months of hire.
Knowledge, Skills & Abilities:
- Ability to prioritize multiple tasks at one time.
- Excellent communication, analytical and organizational skills: both written and verbal.
- Ability to work independently and as part of a team, while being collaborative in resolving problems.
- Proficiency with computers running Windows and PC applications e.g. MS Excel, Word, and PowerPoint.
- Excellent customer service skills.
- Energy and drive to coordinate multiple projects simultaneously.
- Ability to use tact and diplomacy to maintain effective working relationships.
Working Conditions:
- This role will be required to be onsite up to 5 days per week, depending on assignment. Some remote work may be possible, but cannot be guaranteed.
- Must be able to travel to all Knight worksite locations, including using the Portland Ariel Tram.
- Will work with human biological samples, including samples which may contain infectious disease.
- May be expected to travel to conferences, new study meetings, and may travel for study monitoring at other sites.
- Occasional weekend and evening work.
- Ability to focus in a busy cubicle environment with multiple distractions.
Preferred Qualifications:
- Bachelor’s degree with coursework in science or related field.
- At least three years of direct oncology clinical research experience.
- Research experience with some knowledge of clinical trials.
- Experience coordinating different phases of projects, including data collection.
- Customer service experience.
- Microsoft Office, Access, and other networking and database systems.
- Medical terminology.
- OHSU systems Oracle and/or Epic.
Additional Details:
Apply online. Please be sure to upload a Cover Letter and Resume/CV.
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 mission of the Knight Cancer Clinical Research organization is to support the conduct of translational clinical research aimed at improving the lives of people and families with cancer by applying innovative strategies for cancer prevention, screening, diagnosis and treatment. The support is provided through proactive, high quality and efficient study management in compliance with federal regulations and local policies and procedures. This fast-paced and intense research environment requires complex clinical research studies involving a very vulnerable and sick population.
Position Summary:
This TI Clinical Research Associate will be known internally as a Float Clinical Research Associate (Float CRA). It is a collaborative role supporting clinical research programs of the Knight Cancer Clinical Research organization. The Float CRA will support the conduct of translational clinical research aimed at improving the lives of people and families with cancer by applying innovative strategies for cancer prevention, screening, diagnosis, and treatment. The support is provided through proactive, high quality, and efficient study management in compliance with federal regulations and local policies and procedures. This fast-paced and intense research environment requires management of complex clinical research studies involving a vulnerable patient population.
The position will work with different programs within the Knight Cancer Clinical Research operation. They will provide relief, backup, or interim support to maintain progress on critical projects when there are staffing transitions or increased volume. Under occasional supervision, the Float CRA will perform a broad variety of tasks necessary for implementation and overall management of complex therapeutic interventional clinical research. Specific tasks and roles will be determined by the needs of the clinical research program with which the Float CRA is engaged.
These responsibilities will include the coordination of all aspects of a study as specifically outlined in the protocol. Primary focus will be patient safety and compliance with the prescribed protocol and Good Clinical Practice. The Float CRA will work collaboratively with physician, nursing, and ancillary staff in the scheduling and management of subject research activities. The Float CRA will maintain accurate, complete, and timely records on all research subjects including preparation of source documentation and clinical research data/case report forms. The Float CRA may have direct patient contact, process biological samples and may perform other non-invasive testing such as ECGs.
The Float CRA may represent the investigator and institution during monitor visits and on-site audits conducted by the sponsor or sponsor representative. The successful Float CRA will have and maintain a working knowledge of National Cancer Institute (NCI), FDA, DHHS and other agency guidelines that govern clinical research.
Given the complexities of oncology research and the challenges of working with a terminally ill population, strong customer service, organizational, and interpersonal skills are required. The ability to clearly organize and/or adapt to multiple priorities and deadlines at one time is necessary. Attention to detail, service orientation, delegation and project management skills, and above average critical judgment skills are essential. Therapeutic Interventional trials are treatment studies that involve people who have a disease or underlying condition. They include the administration and testing new treatments or new ways of using existing treatments, such as new drugs, vaccines, cell therapies, devices, experimental approaches to surgery or radiation therapy, etc.
OHSU Research classification: TI Clinical Research Associate, represented by the Research Workers United (RWU), subject to the active collective bargaining agreement between OHSU and RWU.
Duties & Responsibilities:
Study Coordination
Responsible for coordinating aspects of oncology clinical trials from startup to closeout and assuring conduct of trials in accordance with NCI and FDA guidelines. This includes but is not limited to:
- Communicate effectively across multiple clinical teams for clinical trial coordination.
- Be able to navigate and understand complex oncology clinical trial protocols.
- Explain trial logistics to oncology patients, triage and ensure all patient questions are answered.
- Assist the PI or Sub-I with the informed consent process.
- Assist the PI or Sub-I with the collection and documentation of subject adverse events.
- Document study required source documentation in the subjects’ medical record or paper source.
- Communicate with the PI or Sub-I during patient visits regarding dose modification parameters.
- Serve as the point of contact for the clinical staff to provide protocol guidance for patient management on trial.
- Triage research patient communications to the personnel most appropriately trained to address their questions/needs.
- Place research lab and procedure orders in compliance with the approved billing schedule.
- Review patient records to screen for potential trials.
- Remove barriers for patients to participate in clinical trials. This may include working with their PCP or local oncologist to get procedures done close to home, connecting them to social work to find travel and financial resources, setting up virtual medicine visits, or referring to another useful resource.
- Perform and document drug accountability.
- Prepare for upcoming visits including reviewing patient records to look for newly reported adverse events, concomitant medications, and other pertinent information to be reviewed with the patient and provider at the visit.
- Submit insurance pre-authorization request for new patients on study.
- Schedule research biopsies, scans, ECHOs/ECGs, Ophthalmology appointments, dermatology visits and other research required procedures as needed.
- Provide clinic training in-services as needed.
- Review patient records to determine eligibility for enrollment into clinical trials. Confirm with the investigator that subject meets appropriate inclusion criteria for clinical trial.
- Communicate all pre-treatment requirements to investigator/clinical staff.
- Obtain and submit imaging studies, pathology, or other samples as required by protocol.
- Verify that procedures/services are billed in accordance with the approved billing schedule.
- Submit Invoices for tasks related to their role.
- Review and report adverse events or Unanticipated Problems to IRB and the study sponsor.
- Obtain vital signs and/or ECG measurements for study patients; conduct protocol-required tests such as the sit-to-stand test or walk test documenting contacts with study subjects as appropriate.
- Procure, process, and ship human biological specimens (including but not limited to blood, urine, feces, sputum, tissue) in adherence with protocol parameters and appropriate training.
- Communicate and facilitate oncology trial guidelines, timelines, and patient specifics with Research Pharmacy, Clinics and various service departments to coordinate treatment for the study patient.
- Ensure compliance with FDA and regulatory reporting agencies.
- Report any non-compliance to study investigator / departmental staff.
- Prepare any necessary materials for required internal and external (sponsor, FDA) regulatory and quality control audits and sponsor monitoring visits.
- May assist and collaborate with principal investigator and sub-principal investigators in clinic during patient appointments, consenting appointments and treatment appointments to ensure protocol is being adhered to and proper documentation is recorded.
Data Management
- Collection and entry of oncology data from patient medical records into study databases.
- Internal tracking and reporting.
- Obtaining and uploading imaging.
- Collaborate with study team to resolve data queries within deadlines.
- Work with study team to correct any quality control issues.
- Collaborate with study representatives to maintain data integrity.
- Lab grading.
- Obtaining study team signatures.
- Scheduling and conducting study monitoring visits.
- Collaborate with the study team to resolve any oncology data queries identified by the study monitor, auditor, or other individual reviewing the study data within tight deadlines with competing priorities.
- Work with the study team to correct any quality control issues with the data entry.
Education and Process Improvement
- Participate in continuing education activities to maintain current knowledge of oncology, research regulatory requirements, and process improvements for clinical trials.
- May assist with or lead training of junior team members.
- May assist or take lead in developing standard procedures for collaboration with clinic operations, sponsor representatives, and across CRM programs.
Audit preparation
- May assist with preparation activities for audit or inspection.
- May perform ad hoc internal monitoring.
Required Qualifications:
Education & Experience:
- Master's Degree in relevant field AND 3 years of clinical research coordination experience OR
- Bachelor's Degree in relevant field AND 5 years of clinical research coordination experience.
- SoCRA or ACRP required within 12 months of hire.
Knowledge, Skills & Abilities:
- Ability to prioritize multiple tasks at one time.
- Excellent communication, analytical and organizational skills: both written and verbal.
- Ability to work independently and as part of a team, while being collaborative in resolving problems.
- Proficiency with computers running Windows and PC applications e.g. MS Excel, Word, and PowerPoint.
- Excellent customer service skills.
- Energy and drive to coordinate multiple projects simultaneously.
- Ability to use tact and diplomacy to maintain effective working relationships.
Working Conditions:
- This role will be required to be onsite up to 5 days per week, depending on assignment. Some remote work may be possible, but cannot be guaranteed.
- Must be able to travel to all Knight worksite locations, including using the Portland Ariel Tram.
- Will work with human biological samples, including samples which may contain infectious disease.
- May be expected to travel to conferences, new study meetings, and may travel for study monitoring at other sites.
- Occasional weekend and evening work.
- Ability to focus in a busy cubicle environment with multiple distractions.
Preferred Qualifications:
- Bachelor’s degree with coursework in science or related field.
- At least three years of direct oncology clinical research experience.
- Research experience with some knowledge of clinical trials.
- Experience coordinating different phases of projects, including data collection.
- Customer service experience.
- Microsoft Office, Access, and other networking and database systems.
- Medical terminology.
- OHSU systems Oracle and/or Epic.
Additional Details:
Apply online. Please be sure to upload a Cover Letter and Resume/CV.
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
See all J-1 Visa Clinical Analyst Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new J-1 Visa Clinical Analyst Jobs.
Get Access To All JobsTips for Finding J-1 Visa Sponsorship as a Clinical Analyst
Align your credentials with specialty occupation evidence
Compile documentation that maps your clinical informatics coursework, healthcare data certifications, or prior analyst work to the specific duties in your host employer's training plan. Designated sponsors evaluate this match before issuing a DS-2019.
Distinguish Trainee from Research Scholar eligibility
Apply under the J-1 Trainee category if you graduated within the last 12 months or are still enrolled. Choose Research Scholar if you hold an advanced degree and your Clinical Analyst role involves systematic data research at a university or medical center.
Target host employers with structured training programs
Health systems, academic medical centers, and large payers are far more likely to support a J-1 training plan than small clinics. Search for Clinical Analyst openings at organizations that already employ exchange visitors across their analytics or informatics departments.
Search J-1-compatible roles using Migrate Mate
Filter for Clinical Analyst positions at U.S. employers with a history of hosting exchange visitors using Migrate Mate. It surfaces roles and organizations whose hiring patterns align with J-1 program requirements, saving you from applying to hosts that have never navigated the DS-2019 process.
Confirm home residency requirement status before accepting
Clinical Analyst placements funded by your home government or a U.S. government agency trigger the two-year home residency requirement. Ask your designated sponsor directly whether your specific funding source activates this requirement before signing an offer.
Request the training plan outline before your start date
USCIS and your designated sponsor both require a completed Form DS-7002 training plan specifying clinical analytics objectives, milestones, and supervision structure. Review it with your host employer before your program begins so the documented activities match your actual role.
Clinical Analyst J-1 Visa: Frequently Asked Questions
Which J-1 program category fits a Clinical Analyst role?
Most Clinical Analyst positions fall under the J-1 Trainee category if you are a recent graduate or current student, or the Research Scholar category if your role involves structured research at a university hospital or academic health system. The Specialist category applies in rare cases where you hold nationally recognized expertise in clinical informatics. Your designated sponsor confirms the correct category based on your qualifications and the host employer's program description.
Who actually sponsors my J-1 visa as a Clinical Analyst?
A U.S. Department of State-designated organization, such as AIPT, Cultural Vistas, or a university's international office, issues your DS-2019 and serves as your legal J-1 sponsor. Your hiring employer is the host site, not the visa sponsor. The host provides the training environment, but the designated sponsor monitors compliance, maintains your SEVIS record, and is responsible for your program integrity throughout your exchange.
How do I find U.S. employers willing to host a J-1 Clinical Analyst?
Use Migrate Mate to identify Clinical Analyst openings at organizations that have hosted exchange visitors before. Health systems affiliated with academic medical centers and large regional payers tend to have the administrative infrastructure to support a J-1 training plan and DS-2019 process. Approaching employers who already understand the host organization obligations reduces friction significantly during the offer stage.
Does a Clinical Analyst J-1 exchange visitor face the two-year home residency requirement?
Potentially. If your J-1 program is funded by your home government, a foreign government, or a U.S. government agency, the two-year home residency requirement applies after your program ends. Clinical Analyst placements at federally funded research hospitals are a common trigger. Your designated sponsor reviews your funding source and notifies you and the State Department if the requirement attaches to your specific DS-2019.
What is a DS-7002 and why does it matter for my Clinical Analyst placement?
The DS-7002 is the formal training and internship placement plan that documents your clinical analytics learning objectives, the supervision structure, and the evaluation schedule at your host employer. Designated sponsors require it before issuing a DS-2019, and USCIS can review it during any status inquiry. A vague or mismatched DS-7002 is a common reason sponsorship is delayed or denied, so confirming that documented duties align with your actual day-to-day responsibilities protects your status.