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Senior Clinical Engineer Jobs (NOW HIRING)

Abbott

Senior R&D Clinical Engineer

Menlo Park, CA · On-site

$123K - $169K/yr

R&D Clinical Engineer Leading an active lifestyle is important to the many people we serve. Abbott's Structural Heart division is a high growth business division working on MitraClip, TriClip ...

Eight Sleep

Senior Clinical Trial Manager

Boston, MA · On-site

The Role We're looking for a Senior Clinical Trials Manager who will own the end-to-end execution ... Collaborate cross-functionally with regulatory affairs, product, engineering, data science, and ...

Abbott

Senior Clinical Specialist

Wilmington, NC

Provides engineering, sales, education and clinical support in response to the most complex field inquiries on as-needed basis. Demonstrates a thorough command of all EP products, related product and ...

Abbott

Senior Clinical Specialist

Jonesboro, AR

Provides engineering, sales, education and clinical support in response to the most complex field inquiries on as-needed basis. Demonstrates a thorough command of all EP products, related product and ...

Abbott

Senior Clinical Specialist

Jonesboro, AR · On-site

Provides engineering, sales, education and clinical support in response to the most complex field inquiries on as-needed basis. Demonstrates a thorough command of all EP products, related product and ...

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Senior Clinical Engineer information

See salary details

$59.5K

$126.6K

$183.5K

How much do senior clinical engineer jobs pay per year?

As of Jul 24, 2026, the average yearly pay for senior clinical engineer in the United States is $126,557.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,500.00 and $143,500.00 per year, depending on experience, location, and employer.

How does a Senior Clinical Engineer typically collaborate with clinical staff and other departments within a healthcare facility?

Senior Clinical Engineers play a key role in bridging the gap between clinical staff and technical teams. They work closely with doctors, nurses, and administrators to ensure medical equipment is safe, effective, and suited to clinical workflows. Regular responsibilities include training clinical staff on new equipment, troubleshooting technical issues, and coordinating with biomedical engineering teams for maintenance schedules. Effective communication and collaboration are essential, as Senior Clinical Engineers often participate in interdisciplinary committees and help develop policies related to equipment usage and safety.

What are the key skills and qualifications needed to thrive as a Senior Clinical Engineer, and why are they important?

To thrive as a Senior Clinical Engineer, you need a solid background in biomedical engineering, medical device technology, and regulatory compliance, often supported by a relevant degree and professional certifications like CBET. Familiarity with hospital information systems, medical device integration platforms, and quality management systems is typically required. Strong analytical thinking, project management, and effective communication skills help you lead teams and collaborate with healthcare professionals. These skills and qualifications ensure safe, efficient implementation and maintenance of medical technology, directly impacting patient care and organizational effectiveness.

What are Senior Clinical Engineers?

Senior Clinical Engineers are experienced professionals who manage and oversee the safe and effective use of medical equipment in healthcare settings. They are responsible for evaluating, maintaining, and improving medical devices, ensuring compliance with safety regulations, and leading teams of junior engineers or technicians. Senior Clinical Engineers often collaborate with medical staff, vendors, and regulatory bodies to support patient care by optimizing technology solutions. Their work plays a critical role in minimizing risks and maximizing the performance of healthcare technology.

What is the difference between Senior Clinical Engineer vs Clinical Engineer?

AspectSenior Clinical EngineerClinical Engineer
CredentialsTypically requires a Bachelor's or Master's in Biomedical Engineering or related field; certifications like CBET or BIOMEDevice are commonSame educational background; certifications may be optional or less advanced
Work EnvironmentHospitals, healthcare facilities, medical device companies; often leads projects and mentors staffHospitals, clinics, medical device maintenance; focuses on equipment installation, calibration, and troubleshooting
Employer & Industry UsageUsed in healthcare and medical device industries; often in larger organizations with senior rolesCommon in healthcare settings; entry to mid-level position

The main difference between a Senior Clinical Engineer and a Clinical Engineer lies in experience, responsibilities, and leadership roles. Senior Clinical Engineers typically have more advanced certifications, oversee complex projects, and mentor junior staff, whereas Clinical Engineers focus on equipment maintenance and support. Both roles are vital in healthcare technology management, but the senior position involves greater oversight and strategic planning.

More about Senior Clinical Engineer jobs
What cities are hiring for Senior Clinical Engineer jobs? Cities with the most Senior Clinical Engineer job openings:
What are the most commonly searched types of Clinical Engineer jobs? The most popular types of Clinical Engineer jobs are:
What states have the most Senior Clinical Engineer jobs? States with the most job openings for Senior Clinical Engineer jobs include:
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Senior Clinical Engineer jobs near you
Infographic showing various Senior Clinical Engineer job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $126,557 per year, or $60.8 per hour.
Manager, Clinical Programming (Remote)

Manager, Clinical Programming (Remote)

Penfield Search Partners

Fairfield, CT • On-site, Remote

Full-time

Posted 7 days ago

Job description

Contact: Neisha Camacho/Terra Parsons -
No 3rd party candidates

Position Summary

We are seeking an experienced Senior Clinical Programmer to support clinical development programs by delivering high-quality programming solutions for medical monitoring, data management, and statistical programming activities. The ideal candidate has strong expertise in CDISC standards, SDTM dataset development, and modern programming tools including SAS and R. This role partners closely with cross-functional teams to develop efficient, compliant, and scalable programming solutions that support ongoing clinical trials.

Key Responsibilities

  • Provide programming support for medical monitoring, data management, and statistical programming activities across clinical studies.
  • Develop specifications for SDTM dataset creation in accordance with CDISC SDTM Implementation Guide (SDTM IG).
  • Program, validate, and maintain CDISC-compliant SDTM datasets.
  • Create and maintain annotated CRFs (aCRFs) aligned with SDTM specifications.
  • Generate outputs and listings to support medical monitoring, data review, statistical endpoint monitoring, and data management activities.
  • Develop, enhance, and maintain SAS macros, R functions, and other reusable programming utilities.
  • Design, develop, test, and implement programming solutions to address complex business and study requirements.
  • Ensure programming deliverables meet quality standards, timelines, and regulatory expectations.
  • Collaborate effectively with cross-functional teams including Biostatistics, Data Management, Clinical Operations, and Medical Monitoring.
  • Manage multiple projects simultaneously while delivering high-quality work within established timelines.

Qualifications

  • Bachelor's degree in Statistics, Computer Science, Mathematics, Life Sciences, or a related discipline (or equivalent experience).
  • Experience programming in the pharmaceutical, biotechnology, or related regulated industry preferred.
  • Advanced programming proficiency in SAS, R, and SQL.
  • Strong working knowledge of CDISC standards, including SDTM and annotated CRFs.
  • Experience with JReview is highly preferred.
  • Experience with Shiny, Pharmaverse, and R Markdown is preferred.
  • Familiarity with programming languages such as Python, VBA, or C++ is a plus.
  • Excellent analytical, problem-solving, and communication skills.
  • Ability to work independently while collaborating effectively within cross-functional teams.
  • Strong organizational skills with the ability to prioritize multiple assignments and meet deadlines.

Preferred Experience

  • Experience supporting medical review or clinical data review activities.
  • Experience developing reusable programming utilities and automation tools.
  • Familiarity with regulatory submission standards and clinical trial data workflows.
  • Experience working in a fast-paced clinical development environment.