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Medical Device Manager Jobs in Nevada (NOW HIRING)

Revvity

Senior Manager, Field Service

Carson City, NV · On-site

Accountable for leading and managing service team leaders, and indirectly, field service engineers ... our medical device products Lead and inspire service team leaders, promoting a culture of ...

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All JobsMedical Device JobsMedical Device Manager JobsMedical Device Manager Jobs in Nevada

Medical Device Manager information

See Nevada salary details

$11

$42

$70

How much do medical device manager jobs pay per hour?

As of Aug 20, 2026, the average hourly pay for medical device manager in Nevada is $42.33, according to ZipRecruiter salary data. Most workers in this role earn between $24.40 and $56.68 per hour, depending on experience, location, and employer.

What is a medical device manager?

Medical Device Managers are professionals responsible for overseeing the development, production, and regulatory compliance of medical devices within healthcare organizations or manufacturing companies. They coordinate teams, manage product lifecycles, ensure products meet safety standards, and liaise with regulatory bodies such as the FDA. Their work helps ensure that medical devices are safe, effective, and brought to market efficiently. In addition, they may also handle budgeting, quality assurance, and post-market surveillance of devices.

What are the key skills and qualifications needed to thrive as a medical device manager?

To excel as a Medical Device Manager, you need a solid background in biomedical engineering, regulatory compliance, and product lifecycle management, often supported by a relevant degree and industry experience. Familiarity with quality management systems (such as ISO 13485), FDA or CE regulatory processes, and CRM or ERP software is typically required. Strong leadership, problem-solving, and communication skills help in guiding cross-functional teams and managing client relationships. These competencies ensure the safe, effective launch and maintenance of medical devices in a highly regulated market.

What are some common challenges faced by medical device managers in ensuring regulatory compliance?

Medical Device Managers often encounter challenges in navigating complex and evolving regulatory requirements across different regions. Ensuring that products meet the standards set by agencies like the FDA or EMA requires continuous monitoring of changes in regulations, thorough documentation, and close collaboration with regulatory affairs and quality assurance teams. Additionally, balancing compliance with timely product development and market launch can be demanding, as even minor oversights can lead to delays or costly recalls.

What is the difference between Medical Device Manager vs Medical Equipment Coordinator?

AspectMedical Device ManagerMedical Equipment Coordinator
CertificationsRegulatory and management certifications, such as RAC or PMPBasic healthcare or equipment management certifications
Work EnvironmentHealthcare facilities, manufacturing companies, regulatory agenciesHospitals, clinics, equipment suppliers
Employer & IndustryMedical device companies, hospitals, biotech firmsHospitals, clinics, medical equipment vendors
Primary FocusOverseeing device development, compliance, and lifecycle managementManaging equipment inventory, maintenance, and distribution

The Medical Device Manager primarily focuses on overseeing the development, compliance, and lifecycle of medical devices, often requiring management certifications. In contrast, the Medical Equipment Coordinator handles equipment inventory, maintenance, and distribution within healthcare settings. Both roles are essential in healthcare but differ in scope and responsibilities.

What are the most commonly searched types of Medical Device jobs in Nevada?

The most popular types of Medical Device jobs in Nevada are:

What are popular job titles related to Medical Device Manager jobs in Nevada?

For Medical Device Manager jobs in Nevada, the most frequently searched job titles are:

What job categories do people searching Medical Device Manager jobs in Nevada look for?

The top searched job categories for Medical Device Manager jobs in Nevada are:

Medical Device Manager jobs near you
Infographic showing various Medical Device Manager job openings in Nevada as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 16% Part Time, and 6% Contract. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $88,044 per year, or $42.3 per hour.

Senior Clinical Research Coordinator

Kyvexa Clinical Trials

Las Vegas, NV

$30/hr

Full-time

Posted 5 days ago

Job description

We are seeking an organized, detail-oriented Clinical Research Study Coordinator to join our team. The Study Coordinator will be responsible for the day-to-day management of clinical studies, including subject screening, informed consent, data entry, regulatory compliance, and coordination with investigators and sponsors. This role is ideal for candidates in research who want to grow in a dynamic, fast-paced clinical research environment.

Compensation 

  • Pay: $25 - $30 per hour based on experience and performance

Schedule

  • Monday to Friday

  • Full-time 

Compensation:

$25 - $30 hourly


Responsibilities:

  • Coordinate and conduct clinical trials according to GCP, ICH, FDA, and sponsor guidelines.

  • Recruit, screen, and enroll eligible study participants.

  • Obtain and document informed consent from subjects.

  • Perform study-related procedures such as specimen collection, vitals, or device use per protocol.

  • Schedule and manage subject visits, ensuring protocol adherence and accurate source documentation.

  • Enter data into Electronic Data Capture (EDC) systems and maintain study binders.

  • Maintain regulatory files, site logs, and documentation readiness for audits or monitoring visits.

  • Communicate with sponsors, CROs, monitors, and physicians regarding study progress and data queries.

  • Ensure subject confidentiality and compliance with HIPAA.

  • Assist in IRB submissions, amendments, and ongoing study correspondence.

  • Traveling required from Kyvexa headquarters to clinics around the Las Vegas Valley and vice versa


Qualifications:

  • Minimum of 1–2 years of clinical or research experience preferred (medical office or lab experience acceptable).

  • Knowledge of GCP, FDA, and ICH guidelines.

  • Strong organizational, multitasking, and time-management skills.

  • Excellent interpersonal and communication skills (bilingual English/Spanish preferred).

  • Computer proficiency with Microsoft Office and EDC systems.

  • Current CPR, Medical Assistant, and Phlebotomist certifications.


About Company

Kyvexa partners with sponsors and investigators to deliver reliable, patient-centered clinical trial site management for medical device research — combining regulatory rigor, operational excellence, and compassionate care to help bring safe, effective devices to market faster. At Kyvexa, we exist to make medical device clinical trials safer and more human — supporting patients, physicians, and sponsors with the highest standards of care, compliance, and integrity.