[Skip to main content](#main-content) [OpenNash Jobs](https://jobs.opennash.com/) [Hiring report](/reports/hiring/) · [All Medtronic jobs](https://jobs.opennash.com/companies/medtronic/) · [Search jobs](/search/) Medtronic · Minneapolis, MN # Sr. Field Clinical Research Specialist Minneapolis, Minnesota, United States of America Senior individual contributor $128,500 to $170,400 per year Healthcare & Clinical Listed on Medtronic’s official careers site. Posted September 22, 2026. Check that it is still open and apply there. [Apply on Medtronic’s careers site →](https://medtronic.wd1.myworkdayjobs.com/MedtronicCareers/job/Minneapolis-Minnesota-United-States-of-America/Sr-Field-Clinical-Research-Specialist_R77878-1) [OpenNash Jobs](https://jobs.opennash.com/) / [Medtronic](https://jobs.opennash.com/companies/medtronic/) / Sr. Field Clinical Research Specialist ## Job description We anticipate the application window for this opening will close on - 27 Nov 2026 Position Description: Sr. Field Clinical Research Specialist for Medtronic, Inc. in Minneapolis, MN. Provide field-based, customer-facing position responsibilities for clinical trial site mgmt., case coverage (clinical and commercial), and clinical trial data tracking. Responsible for conducting clinical studies with adherence to applicable regulations, guidelines, and policies. Prepare and revise Clinical Investigation Plan. Prepare study materials and/or training of investigators, site staff and Medtronic Field staff. Responsible for utilizing Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials including Clinical Trial Design and Execution (Phase I-IV). Coordinate Study Start-up, site initiation, monitoring, and close-out. Leverage Informed Consent Form (ICF), Protocol and amendments development and review. Responsible for Patient recruitment and retention strategies, source document verification (SDV), Adverse event (AE) and Serious adverse event (SAE) reporting. Navigate the complexities of various government and industry regulations including U.S. FDA Regulations 21 CFR Parts 11, 50, 54, 56, 312, and 812, and International Council for Harmonization – Good Clinical Practice (ICH-GCP) E6 R2/R3 Compliance. Coordinate the Institutional Review Board/Independent Ethics Committee (IRB/IEC) submission and approval process. Leverage Corrective and Preventive Actions (CAPA) development and implementation as well as Health Insurance Portability and Accountability Act (HIPAA) compliance. Clinical Trial Mgmt. Systems (CTMS), Veeva Vault CTMS, Oracle Siebel CTMS, and Salesforce. Work within a cardiac catheterization lab directing physicians, nurses, and ancillary staff on how to use products. #LI-DNI Travel domestically up to 75% within assigned territory including Chicago metro area, IL, and Northwest Indiana to provide oversight of clinical trials and case support. Must work remotely from home office within the greater Chicago metro area. Must possess a valid driver’s license and be insurable (car insurance). ### Basic Qualifications Master’s degree in Biological Science, Biology, Nursing, Biomedical Engineering, or Biotechnology and two (2) years of experience as a Clinical Researcher or related occupation in clinical research. Must possess at least two (2) years’ experience with each of the following: GCP and regulatory compliance guidelines for clinical trials including Clinical Trial Design and Execution (Phase I-IV); Clinical study Start-up, site initiation, monitoring, and close-out; Review and development of ICF, Protocol, and amendments; Patient recruitment and retention strategies, SDV, AE and SAE reporting; FDA Regulations 21 CFR Parts 11, 50, 54, 56, 312, 812, and ICH-GCP (E6 R2/R3) Compliance; IRB/IEC Submission and approval process; CAPA development and implementation, and HIPAA compliance; and CTMS, Veeva Vault CTMS, Oracle Siebel CTMS, and Salesforce. Requires travel domestically up to 75% within assigned territory including Chicago metro area, IL, and Northwest Indiana to provide oversight of clinical trials and case support. ### Salary $128,500 to $170,400 per year #LI-DNI The following benefits and additional compensation are available to those regular employees who work 20+ hours per week: Health, Dental and vision insurance, Health Savings Account, Healthcare Flexible Spending Account, Life insurance, Long-term disability leave, Dependent daycare spending account, Tuition assistance/reimbursement, and Simple Steps (global well-being program). The following benefits and additional compensation are available to all regular employees: Incentive plans, 401(k) plan plus employer contribution and match, Short-term disability, Paid time off, Paid holidays, Employee Stock Purchase Plan, Employee Assistance Program, Non-qualified Retirement Plan Supplement (subject to IRS earning minimums), and Capital Accumulation Plan (available to Vice Presidents and above, or subject to IRS earning minimums). Regular employees are those who are not temporary, such as interns. Temporary employees are eligible for paid sick time, as required under applicable state law, and the Employee Stock Purchase Plan. Please note some of the above benefits may not apply to workers in Puerto Rico. ### Further details are available at the link below Medtronic benefits and compensation plans ‌ Recruitment Fraud Alert We are aware of phishing scams targeting job seekers. ### Please keep the following in mind Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate. If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments. If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com. ## At a glance - Posted by the employer: Sep 22, 2026 - First seen by OpenNash: Oct 12, 2026 - Last checked: Oct 19, 2026 - Listed for: 27 days - Location: Minneapolis, Minnesota, United States of America - Pay: $128,500 to $170,400 per year[Apply on Medtronic’s careers site →](https://medtronic.wd1.myworkdayjobs.com/MedtronicCareers/job/Minneapolis-Minnesota-United-States-of-America/Sr-Field-Clinical-Research-Specialist_R77878-1) ## More jobs at Medtronic ### [Clinical Specialist, Pelvic Health - Minneapolis/St.Paul](https://jobs.opennash.com/companies/medtronic/jobs/96acec45834685e1d54a/) Minneapolis, Minnesota, United States of America ### [Principal Medical Safety Specialist](https://jobs.opennash.com/companies/medtronic/jobs/2dbb16fd68146a97c7e7/) Minneapolis, Minnesota, United States of America ### [Senior Medical Science Writer - Onsite](https://jobs.opennash.com/companies/medtronic/jobs/6a35e0a6810ef712e66d/) Minneapolis, Minnesota, United States of America ### [Consents Manager, On-site, Minneapolis, MN](https://jobs.opennash.com/companies/medtronic/jobs/98edee8185660fd8a468/) Minneapolis, Minnesota, United States of America ### [District Sales Manager- Surgical](https://jobs.opennash.com/companies/medtronic/jobs/829053936e95bc32849f/) Minneapolis, Minnesota, United States of America ## Similar jobs at other companies ### [Sr Coordinator, Clinical Research](https://jobs.opennash.com/companies/cardinal-health/jobs/4ce8899f5245a67447e7/) Cardinal Health · Canada ### [Clinical Research Coordinator](https://jobs.opennash.com/companies/thermo-fisher-scientific/jobs/dbf0d2ba95f9cf4db482/) Thermo Fisher Scientific · Atlanta, Georgia, United States of America ### [Clinical Research Coordinator](https://jobs.opennash.com/companies/thermo-fisher-scientific/jobs/c20f5c1eb6d78731e81c/) Thermo Fisher Scientific · Birmingham, Alabama, United States of America ### [Clinical Research Coordinator (DCR)](https://jobs.opennash.com/companies/davita/jobs/66c1f77aff732c1df94f/) DaVita · Ste B, Houston, TX ### [Clinical Research Coordinator (DCR)](https://jobs.opennash.com/companies/davita/jobs/e9508498ea8e3c00ffef/) DaVita · San Antonio, TX OpenNash lists jobs from employers’ own careers sites and does not handle applications. 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