Healthcare F-1 STEM OPT Sponsorship Jobs in Michigan
Healthcare F-1 STEM OPT sponsorship jobs in Michigan are concentrated at major health systems like Henry Ford Health, Beaumont Health, and the University of Michigan Health System, with Detroit, Ann Arbor, and Grand Rapids offering the deepest hiring activity. Roles in health informatics, clinical data analysis, and biomedical engineering are common STEM-designated pathways into Michigan's healthcare sector.
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Get Access To All JobsCareers With Purpose
Sanford Health, the largest rural health system in the United States, is dedicated to transforming the health care experience and providing access to world-class health care in America’s heartland.
Facility: Marsh Med Ctr Iron Mtn
Location: Iron Mountain, MI
Address: 1721 S Suitephenson Ave, Iron Mountain, MI 49801, USA
Shift: 8 Hours - Day Shifts
Job Schedule: Full time
Weekly Hours: 40.00
Salary Range: $20.50 - $33.00
Department Details
In this position you'll gain experience in clinical research and work with oncology clinical trials. This role requires educating patients, physicians, nurses, and other staff about the research process. It also involves organizing all aspects of clinical trials, including outreach, interviewing, scheduling, and coordinating tests and procedures.
Pay starts at $20.50 per hour with additional credit given for work experience relative to this role.
Job Summary
Provides an opportunity to learn daily and contribute to treatments of the future under direction and guidance from leadership. Enthusiasm for learning required, along with participation in educating patients, physicians, nurses and other personnel about the research process. Under specific direction, assist other principal investigators and/or research team by performing basic clinical research duties following established protocols and research related support tasks. Work under direct supervision of a research manager and/or senior research staff (lead) while exhibiting good organizational, communication and interpersonal skills as well as time management.
Assist and organize components of various clinical trials, including the coordination of study-required procedures, as well as investigational treatment for a variety of conditions and symptoms.
Participate with direction in listing and clarifying questions and concerns with the investigator and sponsor regarding enrollment goals, sponsor expectations and study procedures.
Assist with scheduling and coordinating pre-study site visits. Monitor enrollment goals and modify recruitment plan as necessary. Maintain patient screening/enrollment logs and appropriately update sponsors, contract research organizations (CROs) and/or senior medical officers (SMOs). Assure the completion of all screening, eligibility and enrollment procedures and data entry.
Conduct interviews to assess subject ability and willingness to follow and complete study procedures and visits. Follow randomization procedures per protocol. Schedule subjects for follow-up visits. Review diaries and questionnaires completed by subjects. Ensure appropriate specimen collection, batching and shipping as required.
Collect source documents for sponsor or audit review. Assess subject compliance. Abstract data from medical records, clinic, consultation and referral notes for preparation of study forms and flow sheets.
Review inclusion/exclusion criteria to assure subject eligibility, and review with physician investigator for final sign-off. Review and verify required source documents in subject medical records to confirm study eligibility. Review study protocol, informed consent form and follow-up procedures with potential study subjects. Prepare case report forms for sponsor or audit review.
Responsible for insurance pre-authorization for study participation, as applicable by study. Close collaboration with physician investigators required to ensure safe and compliant investigational treatment or intervention and follow-up per the established research protocol.
Document and maintain all study-related procedures, processes and events by planning and designing new forms/source document tools to use in protocol implementation. Document protocol deviations and exemptions. Obtain and review original source documents as needed.
Record accurate and timely data onto case report forms and into the trial data capture system. Maintain source documentation for all case report entries, as applicable. Key in data for electronic submission into the electronic data capture system. Correct and edit case report form entries as appropriate. Resolve data queries. Ensure drug/device accountability by completing appropriate documents per individual protocols.
Schedule and participate in sponsor monitoring visits and audits to ensure compliance with regulatory requirements governing clinical research. Meet with monitors/auditors during routine visits to discuss case report form completion, query resolution and other protocol-related issues. Maintain clinical research department trial supply inventories including destruction of outdated materials, orders for restock and regular reporting of inventory counts to clinical research management.
Occasional local travel between sites and student supervision may be required.
Qualifications
Bachelor's degree in biology, microbiology or related field. May consider graduates of an accredited school of practical nursing as a Licensed Practical Nurse (LPN) dependent on facility and department needs.
Minimum two years of clinical or clinical research experience or four to six years of relevant work experience required.
If a Licensed Practical Nurse (LPN), currently holds an unencumbered LPN license with state nursing board and/or possess multi-state licensure privileges. Obtains and subsequently maintains required department specific competencies and certifications.
Benefits
Sanford offers an attractive benefits package for qualifying full-time and part-time employees. Depending on eligibility, a variety of benefits include health insurance, dental insurance, vision insurance, life insurance, a 401(k) retirement plan, work/life balance benefits, and a generous time off package to maintain a healthy home-work balance. For more information about Total Rewards, visit https://sanfordcareers.com/benefits.
Sanford is an EEO/AA Employer M/F/Disability/Vet. If you are an individual with a disability and would like to request an accommodation for help with your online application, please call 1-877-673-0854 or send an email to talent@sanfordhealth.org.
Sanford has a Drug Free Workplace Policy. An accepted offer will require a drug screen and pre-employment background screening as a condition of employment.
Req Number: R-0258641
Job Function: Research
Featured: No
Careers With Purpose
Sanford Health, the largest rural health system in the United States, is dedicated to transforming the health care experience and providing access to world-class health care in America’s heartland.
Facility: Marsh Med Ctr Iron Mtn
Location: Iron Mountain, MI
Address: 1721 S Suitephenson Ave, Iron Mountain, MI 49801, USA
Shift: 8 Hours - Day Shifts
Job Schedule: Full time
Weekly Hours: 40.00
Salary Range: $20.50 - $33.00
Department Details
In this position you'll gain experience in clinical research and work with oncology clinical trials. This role requires educating patients, physicians, nurses, and other staff about the research process. It also involves organizing all aspects of clinical trials, including outreach, interviewing, scheduling, and coordinating tests and procedures.
Pay starts at $20.50 per hour with additional credit given for work experience relative to this role.
Job Summary
Provides an opportunity to learn daily and contribute to treatments of the future under direction and guidance from leadership. Enthusiasm for learning required, along with participation in educating patients, physicians, nurses and other personnel about the research process. Under specific direction, assist other principal investigators and/or research team by performing basic clinical research duties following established protocols and research related support tasks. Work under direct supervision of a research manager and/or senior research staff (lead) while exhibiting good organizational, communication and interpersonal skills as well as time management.
Assist and organize components of various clinical trials, including the coordination of study-required procedures, as well as investigational treatment for a variety of conditions and symptoms.
Participate with direction in listing and clarifying questions and concerns with the investigator and sponsor regarding enrollment goals, sponsor expectations and study procedures.
Assist with scheduling and coordinating pre-study site visits. Monitor enrollment goals and modify recruitment plan as necessary. Maintain patient screening/enrollment logs and appropriately update sponsors, contract research organizations (CROs) and/or senior medical officers (SMOs). Assure the completion of all screening, eligibility and enrollment procedures and data entry.
Conduct interviews to assess subject ability and willingness to follow and complete study procedures and visits. Follow randomization procedures per protocol. Schedule subjects for follow-up visits. Review diaries and questionnaires completed by subjects. Ensure appropriate specimen collection, batching and shipping as required.
Collect source documents for sponsor or audit review. Assess subject compliance. Abstract data from medical records, clinic, consultation and referral notes for preparation of study forms and flow sheets.
Review inclusion/exclusion criteria to assure subject eligibility, and review with physician investigator for final sign-off. Review and verify required source documents in subject medical records to confirm study eligibility. Review study protocol, informed consent form and follow-up procedures with potential study subjects. Prepare case report forms for sponsor or audit review.
Responsible for insurance pre-authorization for study participation, as applicable by study. Close collaboration with physician investigators required to ensure safe and compliant investigational treatment or intervention and follow-up per the established research protocol.
Document and maintain all study-related procedures, processes and events by planning and designing new forms/source document tools to use in protocol implementation. Document protocol deviations and exemptions. Obtain and review original source documents as needed.
Record accurate and timely data onto case report forms and into the trial data capture system. Maintain source documentation for all case report entries, as applicable. Key in data for electronic submission into the electronic data capture system. Correct and edit case report form entries as appropriate. Resolve data queries. Ensure drug/device accountability by completing appropriate documents per individual protocols.
Schedule and participate in sponsor monitoring visits and audits to ensure compliance with regulatory requirements governing clinical research. Meet with monitors/auditors during routine visits to discuss case report form completion, query resolution and other protocol-related issues. Maintain clinical research department trial supply inventories including destruction of outdated materials, orders for restock and regular reporting of inventory counts to clinical research management.
Occasional local travel between sites and student supervision may be required.
Qualifications
Bachelor's degree in biology, microbiology or related field. May consider graduates of an accredited school of practical nursing as a Licensed Practical Nurse (LPN) dependent on facility and department needs.
Minimum two years of clinical or clinical research experience or four to six years of relevant work experience required.
If a Licensed Practical Nurse (LPN), currently holds an unencumbered LPN license with state nursing board and/or possess multi-state licensure privileges. Obtains and subsequently maintains required department specific competencies and certifications.
Benefits
Sanford offers an attractive benefits package for qualifying full-time and part-time employees. Depending on eligibility, a variety of benefits include health insurance, dental insurance, vision insurance, life insurance, a 401(k) retirement plan, work/life balance benefits, and a generous time off package to maintain a healthy home-work balance. For more information about Total Rewards, visit https://sanfordcareers.com/benefits.
Sanford is an EEO/AA Employer M/F/Disability/Vet. If you are an individual with a disability and would like to request an accommodation for help with your online application, please call 1-877-673-0854 or send an email to talent@sanfordhealth.org.
Sanford has a Drug Free Workplace Policy. An accepted offer will require a drug screen and pre-employment background screening as a condition of employment.
Req Number: R-0258641
Job Function: Research
Featured: No
Healthcare Job Roles in Michigan
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Search Healthcare Jobs in MichiganHealthcare Jobs in Michigan: Frequently Asked Questions
Which healthcare companies sponsor F-1 STEM OPT visas in Michigan?
Michigan's largest health systems are the most active STEM OPT sponsors in the healthcare sector. Henry Ford Health, Michigan Medicine at the University of Michigan, Beaumont Health, Spectrum Health, and Ascension Michigan have all filed Labor Condition Applications for STEM-related healthcare roles. Academic medical centers and research hospitals tend to sponsor more consistently than smaller community practices, because their size supports dedicated HR and immigration compliance teams.
Which cities in Michigan have the most healthcare F-1 STEM OPT sponsorship jobs?
Detroit and its metro area account for the largest share of healthcare STEM OPT roles in Michigan, driven by Henry Ford Health, Detroit Medical Center, and several regional hospital networks. Ann Arbor is a strong secondary market because of Michigan Medicine and the University of Michigan's affiliated research institutes. Grand Rapids, home to Spectrum Health and Corewell Health, is a growing hub for health informatics and clinical technology roles.
What types of healthcare roles typically qualify for F-1 STEM OPT sponsorship?
STEM OPT applies to roles tied to a STEM-designated degree, so the qualifying positions in healthcare tend to be data-intensive or technically specialized rather than direct patient care. Common qualifying roles include health informatics analyst, clinical data scientist, biomedical engineer, healthcare IT specialist, epidemiologist, and bioinformatics researcher. The role's SOC code and the applicant's degree field both need to align with the STEM-designated major listed on the I-20 for the extension to be valid.
How do I find healthcare F-1 STEM OPT sponsorship jobs in Michigan?
Migrate Mate filters job listings specifically for F-1 STEM OPT sponsorship eligibility, so you can search healthcare roles in Michigan without manually screening each employer for sponsorship history. The platform surfaces employers with verified LCA filing records, which is the most reliable signal that a healthcare organization actively sponsors STEM OPT workers. Filtering by Michigan and the healthcare industry narrows results to employers already familiar with the STEM OPT extension process.
Are there state-specific or industry-specific considerations for F-1 STEM OPT sponsorship in Michigan's healthcare sector?
Michigan healthcare employers sponsoring STEM OPT workers must be enrolled in E-Verify, which is a federal requirement for all STEM OPT extensions. Many Michigan health systems already participate in E-Verify because of federal contracting obligations, but smaller regional employers may not. Michigan also has a high concentration of Federally Qualified Health Centers and nonprofit hospital systems, which can have longer internal hiring approval processes that affect how quickly an employer can execute the required training plan documentation under the STEM OPT rules.