Medtronic
Senior Field Clinical Research Specialist RDN
Medtronic, Denver, Colorado, United States, 80285
We anticipate the application window for this opening will close on - 18 Oct 2025
At Medtronic you can begin a life‑long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in the Life At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. This position is remote to enhance our competitive edge and expand our cross‑functional collaboration efforts. It will require 50% – 75% travel to ensure project completion.
Coronary & Renal Denervation therapies are a vital component of the Medtronic Cardiovascular Portfolio. We are passionate about giving patients a “second life” and improved health.
Renal Denervation (RDN) is an innovative procedure that helps patients lower blood pressure by targeting specific nerves near the kidneys. High blood pressure is a global epidemic, affecting one‑third to one‑half of adults.
We are seeking a
Sr. Field Clinical Research Specialist
who will provide technical and educational support to physicians worldwide, launching a new therapy that could transform healthcare in the United States.
Responsibilities
Provides field support for various clinical research studies by selecting sites, performing activation duties, setting up protocols, providing training, enrolling participants, supporting cases, ensuring quality data acquisition and performing study closure activities.
Maintain frequent contact via email/phone/on‑site visits with principal investigators, sub‑investigators, and research coordinators.
Gain and maintain knowledge of clinical sites in a given geographic area to assess investigator interests and capabilities.
Communicate status and performance of multiple studies to in‑house clinical trial leaders.
Assist with overall conduct of assigned clinical studies in compliance with regulations, guidelines, and policies.
Interface with representatives from key functional groups (Monitoring, Data Management, Research & Development, Manufacturing, Sales, Marketing, Regulatory Affairs, Legal, and European Clinical groups).
Identify and mitigate quality risks and issues for assigned clinical studies, overseeing follow‑up and resolution of site issues.
Assist in device allocation, distribution and reconciliation.
Assist with oversight of activities performed by Contract Research Organizations (e.g., CROs, core labs).
Reference SOPs and study management processes for guidance.
Participate in training to enhance knowledge base.
Must Have
Bachelor’s degree with 4+ years of clinical research/clinical experience (e.g., field clinical research/clinical specialist/field clinical engineer).
OR an advanced degree with 2 years of clinical research/clinical experience.
Nice to Have
Hospital/clinical experience.
Experience in Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials.
Certification from a Clinical Research Association (CCRP/CCRC).
Experience at Medtronic or within the medical device industry.
Experience in the management of clinical devices.
Cardiovascular/cardiac rhythm management device training (e.g., pacemakers & defibrillators).
Experience in a Cath lab, biomedical engineering, hospital/clinic or medical sales.
Experience in clinical studies and/or trial site management/protocols.
Experience collaborating with cross‑functional clinical partners/customers, physicians and/or medical sales colleagues in the healthcare industry.
Physical Job Requirements The required physical demands are representative of essential functions of this job. Reasonable accommodations may be made for individuals with disabilities.
Benefits & Compensation Salary ranges for U.S. (excluding Puerto Rico) locations: $108,000.00 – $162,000.00. This position is eligible for a short‑term incentive called the Medtronic Incentive Plan (MIP).
Benefits include Health, Dental & Vision insurance, Health Savings Account, Healthcare FSA, Life insurance, Long‑term disability, Dependent daycare, Tuition assistance, 401(k) with employer match, Paid time off, Employee Stock Purchase Plan, and more.
For further details, please visit the Medtronic benefits page.
Equal Employment Opportunity (EEO) Medtronic is an equal opportunity employer. In addition to all applicable laws, we provide reasonable accommodations for qualified individuals with disabilities.
Application Information For updates on job applications, please go to the candidate login page. If you need assistance completing your application, please email AskHR@medtronic.com.
To request removal of your personal information, email RS.HRCompliance@medtronic.com.
#J-18808-Ljbffr
At Medtronic you can begin a life‑long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.
A Day in the Life At Medtronic, we push the limits of what technology, therapies and services can do to help alleviate pain, restore health and extend life. We challenge ourselves and each other to make tomorrow better than yesterday. This position is remote to enhance our competitive edge and expand our cross‑functional collaboration efforts. It will require 50% – 75% travel to ensure project completion.
Coronary & Renal Denervation therapies are a vital component of the Medtronic Cardiovascular Portfolio. We are passionate about giving patients a “second life” and improved health.
Renal Denervation (RDN) is an innovative procedure that helps patients lower blood pressure by targeting specific nerves near the kidneys. High blood pressure is a global epidemic, affecting one‑third to one‑half of adults.
We are seeking a
Sr. Field Clinical Research Specialist
who will provide technical and educational support to physicians worldwide, launching a new therapy that could transform healthcare in the United States.
Responsibilities
Provides field support for various clinical research studies by selecting sites, performing activation duties, setting up protocols, providing training, enrolling participants, supporting cases, ensuring quality data acquisition and performing study closure activities.
Maintain frequent contact via email/phone/on‑site visits with principal investigators, sub‑investigators, and research coordinators.
Gain and maintain knowledge of clinical sites in a given geographic area to assess investigator interests and capabilities.
Communicate status and performance of multiple studies to in‑house clinical trial leaders.
Assist with overall conduct of assigned clinical studies in compliance with regulations, guidelines, and policies.
Interface with representatives from key functional groups (Monitoring, Data Management, Research & Development, Manufacturing, Sales, Marketing, Regulatory Affairs, Legal, and European Clinical groups).
Identify and mitigate quality risks and issues for assigned clinical studies, overseeing follow‑up and resolution of site issues.
Assist in device allocation, distribution and reconciliation.
Assist with oversight of activities performed by Contract Research Organizations (e.g., CROs, core labs).
Reference SOPs and study management processes for guidance.
Participate in training to enhance knowledge base.
Must Have
Bachelor’s degree with 4+ years of clinical research/clinical experience (e.g., field clinical research/clinical specialist/field clinical engineer).
OR an advanced degree with 2 years of clinical research/clinical experience.
Nice to Have
Hospital/clinical experience.
Experience in Good Clinical Practice (GCP) and regulatory compliance guidelines for clinical trials.
Certification from a Clinical Research Association (CCRP/CCRC).
Experience at Medtronic or within the medical device industry.
Experience in the management of clinical devices.
Cardiovascular/cardiac rhythm management device training (e.g., pacemakers & defibrillators).
Experience in a Cath lab, biomedical engineering, hospital/clinic or medical sales.
Experience in clinical studies and/or trial site management/protocols.
Experience collaborating with cross‑functional clinical partners/customers, physicians and/or medical sales colleagues in the healthcare industry.
Physical Job Requirements The required physical demands are representative of essential functions of this job. Reasonable accommodations may be made for individuals with disabilities.
Benefits & Compensation Salary ranges for U.S. (excluding Puerto Rico) locations: $108,000.00 – $162,000.00. This position is eligible for a short‑term incentive called the Medtronic Incentive Plan (MIP).
Benefits include Health, Dental & Vision insurance, Health Savings Account, Healthcare FSA, Life insurance, Long‑term disability, Dependent daycare, Tuition assistance, 401(k) with employer match, Paid time off, Employee Stock Purchase Plan, and more.
For further details, please visit the Medtronic benefits page.
Equal Employment Opportunity (EEO) Medtronic is an equal opportunity employer. In addition to all applicable laws, we provide reasonable accommodations for qualified individuals with disabilities.
Application Information For updates on job applications, please go to the candidate login page. If you need assistance completing your application, please email AskHR@medtronic.com.
To request removal of your personal information, email RS.HRCompliance@medtronic.com.
#J-18808-Ljbffr