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Remote Biomedical Device Jobs (NOW HIRING)

Be involved in the medical device software design controls activities, in accordance with the FDA ... S. or higher preferred in Computer Science, Software Engineering, Informatics, Biomedical, or ...

Be involved in the medical device software design controls activities, in accordance with the FDA ... S. or higher preferred in Computer Science, Software Engineering, Informatics, Biomedical, or ...

Be involved in the medical device software design controls activities, in accordance with the FDA ... S. or higher preferred in Computer Science, Software Engineering, Informatics, Biomedical, or ...

We are seeking a dynamic and results-driven Medical Device Sales Engineer to drive the growth of ... Bachelor's degree in engineering or a scientific discipline (e.g., biomedical engineering ...

Remote, United States Reports To: VP Clinical Affairs About the Company VahatiCor is a medical ... Qualifications • Bachelor's degree in biomedical engineering, life sciences, cardiovascular ...

Possess a solid understanding of clinical research (pharma/device/biotech) and of clinical research ... Minimum of 8 years experience in clinical/biomedical and/ or software development environment ...

In this role, you will provide remote technical support for customerreported hardware and software ... Medical Device Industry background preferred * Proficient in electro-mechanical products is ...

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Remote Biomedical Device information

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$36.5K

$78K

$116K

How much do remote biomedical device jobs pay per year?

As of Jun 29, 2026, the average yearly pay for remote biomedical device in the United States is $78,021.00, according to ZipRecruiter salary data. Most workers in this role earn between $47,500.00 and $98,500.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Remote Biomedical Device Specialist, and why are they important?

To thrive as a Remote Biomedical Device Specialist, you need a strong background in biomedical engineering, device troubleshooting, and regulatory compliance, usually supported by a relevant degree or certification. Familiarity with remote monitoring software, electronic health records (EHR) integration, and device-specific platforms is essential. Exceptional problem-solving skills, attention to detail, and effective communication are crucial for supporting clinicians and patients remotely. These skills ensure safe, efficient operation and support of medical devices, directly impacting patient outcomes and regulatory adherence.

What is the difference between Remote Biomedical Device vs Remote Biomedical Engineer?

AspectRemote Biomedical DeviceRemote Biomedical Engineer
CredentialsTypically requires biomedical device certifications, technical trainingRequires biomedical engineering degree, professional licensure often preferred
Work EnvironmentPrimarily product testing, troubleshooting, remote supportDesign, development, analysis of biomedical devices, often collaborative
Employer & Industry UsageMedical device companies, healthcare tech firmsHospitals, medical device manufacturers, research institutions
Search & Comparison IntentFocus on device-specific roles, troubleshooting, supportFocus on engineering design, development, innovation

Remote Biomedical Device roles typically involve supporting, testing, and troubleshooting medical devices remotely, often requiring technical certifications. Remote Biomedical Engineers focus on designing and developing medical devices, requiring a biomedical engineering degree. Both roles are integral to the healthcare industry but differ in responsibilities and required credentials.

What are some unique challenges faced by professionals working remotely in biomedical device roles?

Working remotely in biomedical device roles often involves overcoming challenges related to hands-on hardware testing and collaboration with multidisciplinary teams. Since device development and troubleshooting may require physical interaction with prototypes, remote professionals need to rely heavily on clear communication, detailed documentation, and virtual tools for effective teamwork. Additionally, coordinating with on-site engineers and staying updated on regulatory compliance can require extra effort when not physically present. However, remote roles can also offer flexibility and exposure to a broader range of projects and teams.

What is a remote biomedical device?

A remote biomedical device is a medical instrument or system that monitors, diagnoses, or treats patients from a distance, often transmitting data wirelessly to healthcare professionals. These devices can include wearable monitors, implantable sensors, or home-use medical equipment that allows for continuous patient care without the need for frequent hospital visits. Remote biomedical devices are increasingly important for managing chronic diseases, post-surgical recovery, and elderly care, as they enable real-time health tracking and timely intervention. They help improve patient outcomes and reduce healthcare costs by allowing clinicians to make informed decisions based on real-time data.
More about Remote Biomedical Device jobs
What cities are hiring for Remote Biomedical Device jobs? Cities with the most Remote Biomedical Device job openings:
What are the most commonly searched types of Biomedical Device jobs? The most popular types of Biomedical Device jobs are:
What states have the most Remote Biomedical Device jobs? States with the most job openings for Remote Biomedical Device jobs include:
Sr. Clinical Research Associate (Field)

Sr. Clinical Research Associate (Field)

Shifamed

Los Gatos, CA • On-site, Remote

$120K - $140K/yr

Full-time

Posted 25 days ago


Key responsibilities

  • Monitor patient data and clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.

  • Lead and conduct on-site and remote monitoring visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.

  • Serve as the primary point of contact for investigative sites, fostering strong and collaborative site relationships.


Job description

Supira Medical, a clinical-stage Shifamed Portfolio Company, is developing a low-profile, high continuous flow percutaneous ventricular assist device (pVAD) to provide temporary mechanical circulatory support in high risk percutaneous coronary interventional (HRPCI) procedures as well as patients suffering from cardiogenic shock. To learn more about Supira Medical, please visit www.supiramedical.com.
ABOUT SHIFAMED
Founded in 2009 by serial entrepreneur Amr Salahieh, Shifamed LLC is a privately held medical device innovation hub focused on the development of novel medical products to address clinical needs in the rapidly evolving fields of cardiology and ophthalmology.
Description:

We are seeking one field-based Senior Clinical Research Associate (Senior CRA) who will play a critical role in monitoring and managing clinical trial site activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle. These are full time, remote positions with anticipated travel of up to 80%.

Preferred geographic locations: GA, NC, SC, TN, or VA

  • Southeast (1): GA, NC, SC, TN, or VA
Responsibilities, Skills amp; Hands-On Experience:
  • Serve as the primary point of contact for investigative sites, fostering strong and collaborative site relationships.
  • Monitor patient data and clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Lead and conduct on-site and remote monitoring visits (site qualification, initiation, monitoring, and close-out) to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Critically review clinical data to ensure accuracy, completeness, and integrity in alignment with EDC systems and clinical data management standards.
  • Engage site staff in development of enrollment targets, tracking enrollment progress, and troubleshooting patient recruitment issues.
  • Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Maintain oversight of investigational product accountability, tracking, and reconciliation for cardiovascular devices.
  • Partner closely with internal stakeholders to align clinical activities with business and regulatory objectives.
  • Identify, document, and assist in resolving protocol deviations and CAPAs.
  • Participate in internal audits and support readiness for regulatory inspections.
Education amp; Work Experience:
  • Bachelor’s degree in life sciences, nursing, biomedical engineering, or related discipline.
  • 5+ years of experience in clinical research, including at least 3 years of independent monitoring for medical device trials. Experience in IDE studies strongly preferred.
  • Prior experience in cardiovascular or interventional device studies strongly preferred.
  • Strong working knowledge of GCP, ISO 14155 and FDA guidelines.
  • Proficient in EDC, eTMF, and Microsoft Office tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
Our salary ranges are calculated by role, level, and location. Please note that your position within that range will be determined by your job-related knowledge, location, skills, experience, relevant education, and training/certifications. The base salary range for this full-time position is between $120,000 - $140,000 + equity + benefits.
NOTICE TO CANDIDATES: Please be aware that Shifamed and its portfolio companies do not conduct interviews or extend offers through mobile web chat applications. Please report any such occurrences to hr@shifamed.com.