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Clinical Engineer Jobs in Portland, OR (NOW HIRING)

Trimedx

Network Director, Clinical Engineering

Vancouver, WA · On-site

$104K - $135K/yr

Summary The Network Director Clinical Engineering leads clinical engineering initiatives to provide superior customer service and operational efficiency by managing the execution of the TRIMEDX ...

RXinsider LTD.

Clinical Associate

Portland, OR · On-site

$51 - $101/hr

What You'll Work On Working under general direction, provides engineering, sales, educational and ... As a Clinical Associate on the U.S. Abbott EP team, you will provide clinical and technical support ...

Teen Challenge USA

CLINICAL DIRECTOR

Milwaukie, OR · On-site

$120 - $170/hr

Own the design and continuous improvement of individual, family, and group therapy and psychosocial rehabilitation programming. * Build and monitor clinical protocols for intake, assessment ...

Adult and Teen Challenge

CLINICAL DIRECTOR

Milwaukie, OR · On-site

$85K - $116K/yr

... programming. • Build and monitor clinical protocols for intake, assessment, treatment planning, and discharge - grounded in evidence-based practice. • Track clinical outcomes and quality metrics ...

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All JobsClinical Engineer JobsClinical Engineer Jobs in Portland, OR

Clinical Engineer information

See Portland, OR salary details

$43K

$99.4K

$144.2K

How much do clinical engineer jobs pay per year?

As of Sep 6, 2026, the average yearly pay for clinical engineer in Portland, OR is $99,369.00, according to ZipRecruiter salary data. Most workers in this role earn between $74,200.00 and $116,100.00 per year, depending on experience, location, and employer.

What is a clinical engineer?

A clinical engineer collaborates with scientists to develop medical equipment and biomedical research advances. Testing and designing medical technology are their primary responsibilities. Your work may involve artificial tissues, such as joints, hearing implants, and heart valves; pharmaceuticals; medical instruments; or diagnostic equipment, like imaging machines and monitoring apparatus. Job duties include maintaining biomedical equipment and computer systems, overseeing teams of technicians, and leading research studies in biomedical technology.

What does a clinical engineer do?

A Clinical Engineer is a professional who applies engineering principles to the healthcare field, particularly in medical technology and equipment management within hospitals and clinics. Their main responsibilities include ensuring the safe and effective use of medical devices, maintaining and troubleshooting equipment, and providing technical support to medical staff. Clinical Engineers may also be involved in equipment procurement, regulatory compliance, and training users on new technologies. By bridging the gap between engineering and medicine, they help improve patient care and safety.

What are the key skills and qualifications needed to thrive as a clinical engineer, and why are they important?

To thrive as a Clinical Engineer, you need a strong background in biomedical engineering, electronics, and healthcare technology, typically supported by a relevant degree and sometimes professional certification (e.g., CCE). Familiarity with medical device regulations, hospital equipment management systems, and quality assurance tools is essential. Excellent problem-solving, communication, and teamwork skills help Clinical Engineers collaborate with medical staff and address complex technical issues. These abilities are critical for ensuring the safety, compliance, and optimal performance of medical devices in healthcare environments.

How does a clinical engineer typically interact with clinical staff and medical device vendors in a healthcare setting?

Clinical Engineers play a pivotal role in bridging the gap between medical technology and clinical practice. They regularly collaborate with clinical staff to ensure that medical equipment is used safely and efficiently, providing training and addressing any technical concerns. Additionally, Clinical Engineers coordinate with device vendors for equipment maintenance, troubleshooting, and upgrades, often acting as the primary point of contact during installations or when evaluating new technologies. This collaborative environment requires strong communication skills and a proactive approach to problem-solving, making teamwork a central aspect of the role.

What is the difference between Clinical Engineer vs Biomedical Equipment Technician?

AspectClinical EngineerBiomedical Equipment Technician
CredentialsBachelor's degree in engineering or related field; certifications like CBET or CCEAssociate's or bachelor's degree; certifications like CBET or CRES
Work EnvironmentDesign, evaluate, and oversee medical equipment; collaborate with healthcare staffMaintain, repair, and calibrate medical devices on-site in healthcare facilities
Employer & IndustryHospitals, medical device companies, healthcare institutionsHospitals, clinics, biomedical service companies

Clinical Engineers focus on the design, evaluation, and management of medical equipment, often working on system integration and safety protocols. Biomedical Equipment Technicians primarily handle the maintenance, repair, and calibration of medical devices. Both roles are essential in healthcare settings, but Clinical Engineers typically have a broader scope involving engineering principles and system oversight, while Biomedical Equipment Technicians focus on hands-on equipment servicing.

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The top searched job categories for Clinical Engineer jobs in Portland, OR are:

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Clinical Engineer jobs near you
Infographic showing various Clinical Engineer job openings in Portland, OR as of August 2026, with employment types broken down into 2% As Needed, 78% Full Time, 14% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $99,369 per year, or $47.8 per hour.

Clinical Studies Engineer II

Biotronik

Lake Oswego, OR • On-site

Full-time

Posted 12 days ago

Key responsibilities

  • Participate in all phases of clinical investigations, including study design, initiation, enrollment, study execution, data analysis, and clinical report writing.

  • Lead the development and revision of clinical study protocols and design case report forms to support data collection and analysis.

  • Provide day-to-day study management and support to investigative sites, including training, monitoring, and resolving data discrepancies.

Job description

Clinical Studies Engineer II
BIOTRONIK is one of the leading manufacturers of cardio- and endovascular implants and catheters for cardiac rhythm management, electrophysiology and vascular intervention. As a globally active company headquartered in Berlin, Germany, we develop, produce and distribute high-quality medical products based on the latest technology and research. Our success is based on the competence and results-oriented cooperation of our employees.
BIOTRONIK is seeking a Clinical Studies Engineer II to join our Clinical Studies team. In this role, you will play an important part in the planning, execution, and successful completion of clinical investigations involving innovative medical device technologies. You will develop an in-depth understanding of BIOTRONIK products, clinical procedures, and relevant therapeutic areas while serving as a clinical and technical resource for investigative sites, field personnel, and internal stakeholders. Working collaboratively with cross-functional teams, investigators, and study sites, you will support clinical investigations throughout the study lifecycle, including protocol development, study initiation, enrollment, data analysis, clinical reporting, and regulatory submissions. This role offers the opportunity to contribute to the development of clinical evidence supporting BIOTRONIK technologies while helping ensure the successful and compliant conduct of clinical studies.
Your Responsibilities
Clinical Study Management & Execution
  • Participate in all phases of clinical investigations, including study design, initiation, enrollment, study execution, data analysis, and clinical report writing.
  • Lead the development and revision of clinical study protocols.
  • Design case report forms (CRFs) to support accurate, comprehensive data collection and analysis in accordance with study protocols.
  • Develop study documents, training materials, and other resources supporting clinical protocols, study procedures, and CRF completion.
  • Provide day-to-day study management and support to investigative sites.
  • Serve as a clinical and technical resource for site coordinators, investigators, field clinical personnel, sales representatives, and other internal stakeholders.
  • Train investigative sites and BIOTRONIK personnel on clinical protocols, investigational devices, study procedures, and data collection requirements.
  • Support sites and field personnel in collecting complete, accurate, timely, and compliant clinical data.
  • Review and/or monitor case report forms, source documents, and other study records in accordance with BIOTRONIK procedures and applicable regulatory requirements.
  • Collaborate with study teams, field personnel, and investigative sites to resolve data discrepancies, compliance concerns, and regulatory issues.
  • Identify and report significant protocol compliance issues and support appropriate resolution.
  • Develop solutions to logistical and operational challenges that arise during study execution and communicate recommendations to appropriate stakeholders.
  • Build and maintain strong professional relationships with investigators and investigative sites.

Data Analysis, Reporting & Regulatory Support
  • Partner with Clinical Data Operations to clean, organize, summarize, and analyze complex clinical data.
  • Generate clinical reports and contribute to scientific publications.
  • Support preparation of clinical content for FDA submissions.
  • Participate in FDA meetings as a clinical representative when needed, including presenting and explaining device features, clinical study design, and study results.

Product & Technical Expertise
  • Develop an in-depth understanding of BIOTRONIK products and associated clinical procedures, which may include technologies within cardiac rhythm management, vascular intervention, and/or spinal cord stimulation.
  • Develop training and clinical study support materials for investigational or study devices and procedures.
  • Collaborate with Advanced Product Support and other internal teams to address technical and study-related questions.
  • Attend device implants and/or follow-up procedures as needed to remain current on devices, clinical utilization, and patient care.
  • Provide clinical and technical feedback to Engineering and Research & Development teams as needed.
  • Contribute clinical expertise to new project planning and development initiatives.
  • Support the training and mentoring of newly hired Clinical Studies Engineers.
  • Provide support to other clinical studies and projects as business needs require.

What We're Looking For
Required Qualifications
  • Bachelor's degree in a health profession, science, engineering, or related field with a strong technical and clinical background.
  • Working knowledge of FDA regulations, ICH guidelines, Good Clinical Practice (GCP), and other regulations and standards governing clinical research.
  • Demonstrated ability to develop expertise in relevant therapeutic areas and quickly learn and integrate knowledge of new technologies and clinical applications.
  • Strong written and verbal communication, presentation, and interpersonal skills.
  • Excellent organizational skills and attention to detail.
  • Ability to manage multiple priorities and work effectively both independently and as part of a cross-functional team.
  • Strong computer skills and ability to work effectively with clinical study data and documentation.

Clinical Studies Experience
Candidates must meet one of the following:
  • More than three years of successful experience as a Clinical Studies Engineer I within BIOTRONIK's Clinical Studies department, along with completion of Clinical Studies Certification in a product area of primary study support; or
  • Comparable clinical studies experience with another organization in a similar position or relevant field.

Preferred Qualifications
  • Master's degree in a health profession, science, engineering, or related discipline.
  • Experience in a clinical setting, biostatistics, IDE clinical studies, and/or medical device support.
  • Previous experience supporting medical device clinical investigations.

Work Location
Work location is hybrid out of our Lake Oswego, Oregon campus -or- remote within the United States based on skill set and qualifications.
Travel Requirements
  • Travel is generally limited to less than two weeks per year for clinical procedures, investigative site training, and meetings. Depending on study needs and the phase of a clinical investigation, travel may periodically increase to up to 25%.

Physical Requirements
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
While performing the duties of this job, the employee is regularly required to be independently mobile.
  • The employee is also required to interact with a computer for extended periods of time, and communicate with co-workers.
  • Must be able to work a minimum of 40 hours / week.
  • Must be able to travel

Are you interested? Please apply online through our application management system! We are looking forward to welcoming you.
Location: Lake Oswego, OR | Working hours: Full-time | Type of contract: Undefined
Apply now under: www.biotronik.com/careers
Job ID: 62605 | USA | BIOTRONIK Inc.
We are an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin, disability status, protected veteran status, genetic information, or any other characteristic protected by law. Please note that applications sent by post will only be returned if a sufficiently stamped self-addressed envelope is included.

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