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Clinical Development Engineer Jobs (NOW HIRING)

Primary Function of the Position The Sr. Clinical Development Engineer, Multiport Instruments (CDE) uses their in-depth knowledge of the surgical environment and medical technology to work with ...

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Clinical Development Engineer information

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$40.5K

$93.7K

$136K

How much do clinical development engineer jobs pay per year?

As of Jun 15, 2026, the average yearly pay for clinical development engineer in the United States is $93,700.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $109,500.00 per year, depending on experience, location, and employer.

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

To thrive as a Clinical Development Engineer, you need a solid background in biomedical engineering or a related field, along with experience in clinical trials and medical device development. Familiarity with regulatory standards (such as FDA or ISO), clinical data management systems, and proficiency in technical documentation tools are typically required. Strong problem-solving abilities, attention to detail, and effective communication skills help you excel in cross-functional teams and stakeholder interactions. These skills ensure safe, compliant, and innovative product development that meets both clinical and regulatory requirements.

What is the difference between Clinical Development Engineer vs Clinical Research Associate?

AspectClinical Development EngineerClinical Research Associate
Required credentialsBachelor's in engineering, life sciences, or related field; sometimes certifications in clinical engineeringBachelor's in life sciences, health sciences, or related; often clinical research certifications
Work environmentDesign, develop, and test medical devices; collaborate with engineering teamsMonitor clinical trials; ensure compliance with protocols and regulations
Employer & industry usageMedical device companies, biotech firms, hospitalsPharmaceutical companies, contract research organizations, hospitals

While both roles support healthcare innovation, Clinical Development Engineers focus on designing and testing medical devices, whereas Clinical Research Associates oversee clinical trials to ensure regulatory compliance. Both require knowledge of medical regulations but serve different stages of product development and clinical testing.

What are some typical challenges a Clinical Development Engineer faces when transitioning medical devices from prototype to clinical trials?

A Clinical Development Engineer often encounters challenges related to regulatory compliance, ensuring the device meets stringent safety and efficacy standards before clinical trials can proceed. Coordinating between cross-functional teams—such as R&D, regulatory affairs, and clinical operations—can also present difficulties, as aligning timelines and requirements is crucial. Additionally, adapting the prototype based on feedback from preclinical and pilot studies requires flexibility and technical problem-solving skills. Successfully navigating these challenges is essential for advancing medical devices to market.

What is a Clinical Development Engineer?

A Clinical Development Engineer is a professional who works at the intersection of engineering, clinical research, and healthcare. They are responsible for designing, developing, and evaluating medical devices or technologies used in clinical settings. Their role often involves collaborating with clinicians, conducting clinical trials, ensuring compliance with regulations, and translating clinical needs into engineering solutions. These engineers help bridge the gap between innovative technology and patient care, ensuring that devices are safe, effective, and user-friendly.
Infographic showing various Clinical Development Engineer job openings in the United States as of June 2026, with employment types broken down into 1% As Needed, 84% Full Time, and 15% Part Time. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $93,700 per year, or $45 per hour.
Clinical Development Engineer

Clinical Development Engineer

Calyxo, Inc.

Pleasanton, CA

Other

Medical, Retirement, PTO

Posted 19 days ago


Job description

Calyxo, Inc. is a medical device company headquartered in Pleasanton, California, USA. The company was founded in 2016 to address the profound need for improved kidney stone treatment. Kidney stone disease is a common, painful condition that consumes vast amounts of healthcare resources each year. Our team is led by executives and investors with a proven track record of commercializing paradigm-shifting devices to meet unmet needs within urology.

Are you ready to change the future of kidney stone treatment? We are seeking high achievers who want to be part of a dynamic team working in a fun, diverse atmosphere.

Summary:

This position is responsible for providing clinical insights to support new product development and evidence generation through bench and animal model testing. The ideal candidate will also contribute to enhancing procedural excellence and refining current Calyxo commercial product offerings. Additionally, this role will assist in defining customer requirements and participate in physician evaluations during in-vitro bench testing, simulated-use studies, and in-vivo testing as needed for new product development.

In This Role, You Will:

  • Become an expert on the clinical application of Calyxo Inc's products, kidney stone disease state and treatment, and the competitive landscape.
  • Develop in vitro and in vivo kidney models for evidence generation, technique optimization, training, and new product development. Research literature as needed to gather anatomical data necessary to develop appropriate in-vitro models.
  • Support the development and execution of test methods for evaluating and comparing the performance of devices (Company's and competitive products) for marketing analysis and collateral, evidence generation, concept selection, design optimization, design verification & validation.
  • Contribute to the development of customer input requirements and support associated design validation testing plans, protocols, and test execution.
  • Support design and manage in-vitro, ex-vivo, and in-vivo product testing: study design, model design/development, and selection.
  • Collaborate with development teams to prepare and conduct physician evaluation sessions, including method/test sequence development, model design/selection, and data collection.
  • Ensure procedural excellence with Calyxo Inc products by combining engineering product knowledge, understanding of the complaints data, and in-field analysis of product performance.
  • Establish best practices for procedural techniques for field and customer training and to provide insights for new product development.
  • Evaluate and analyze procedural data including case videos, physician questionnaires, and complaints data.
  • Lead cross-functional alignment with Marketing, R&D and Professional Education to incorporate procedural best practices learnings into training materials.
  • Collaborate with Marketing and R&D to define clinical performance goals and perform risk assessments. Validate performance of the device relative to those goals.
  • Proctor cases evaluating advanced techniques. Create plans and systems to collect data from these initiatives.

Who You Will Report To:

  • Director, Clinical Development Engineering

Requirements:

  • BS in Engineering or related discipline with 5+ years related experience in the medical device industry; MS with 3+ years experience or PhD. Biomedical Engineering degree is a plus.
  • 2+ years previous experience in medical device clinical engineering-related activities strongly preferred (participating in conducting animal studies, in-vitro testing, etc).
  • Strong background in hypothesis development and experimental testing, ideally within an academic or research setting
  • Prior experience interfacing directly with physicians in a surgical setting is strongly preferred.
  • Knowledge of and exposure to product testing and data collection required.
  • Experience in endourological procedures, techniques, devices, and pre-clinical testing is preferred.
  • Ability to travel 30%
  • Excellent interpersonal and negotiating skills; ability to adapt to changing work priorities
  • Polished communicator and presenter with excellent listening, teaching, and program evaluation skills.
  • Effective interpersonal interactions, both within the commercial group and in accounts
  • Proficiency with PC-based office computers, including familiarity with Microsoft Word, Excel, PowerPoint, and Outlook required
  • Ability to work independently
  • Valid driver's license
  • Compliance with relevant county, state, and Federal rules regarding vaccinations.

What We Offer:

At Calyxo, you will be part of a knowledgeable, high-achieving, experienced and fun team. You will work in a diverse work environment with experienced, proven leaders and have an opportunity to shape our company culture. You will experience constant learning and dynamic challenges to help you grow and be the best version of yourself.

We also offer an attractive compensation package, which includes:

  • A competitive base salary range of $120,000 - $140,000 and variable incentive plan
  • Stock options - ownership and a stake in growing a mission-driven company
  • Employee benefits package that includes 401(k), healthcare insurance and paid vacation

Calyxo is deeply committed to fostering an environment where diversity and inclusion are not only valued but also prioritized. We believe a diverse and inclusive community empowers us to act courageously, care deeply, and dream boldly to impact people in big ways. Diverse viewpoints bring diverse capabilities, which strengthen our focus and fuel our growth.

Calyxo is proud to be an equal opportunity employer, seeking to create a welcoming and diverse environment. All applicants will receive consideration for employment without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, disability, age, veteran status or any other applicable legally protected characteristics

Legal authorization to work in the United States is required. In compliance with federal law, all persons hired will be required to verify their identity and eligibility to work in the United States and to complete the required employment eligibility verification form upon hire.

Disclaimer:

At Calyxo, we prioritize a transparent and structured interview process to ensure the best fit for both our candidates and our team. Please be aware of the following:

  • Structured Interview Process: Our hiring process includes multiple stages of interviews where you will have the opportunity to communicate directly with Calyxo employees. This ensures that you gain a comprehensive understanding of the role and our company culture.
  • Verification of Identity: We do not extend job offers without first meeting candidates, either virtually or in person. This step is crucial to maintain the integrity of our hiring process and to ensure mutual alignment.
  • Beware of Scams: Calyxo will never request sensitive personal information, such as your full name, address, phone number, or identification documents, via email or online forms before an official interview. Calyxo representatives will always contact you using an email format of firstname.lastname@calyxoinc.com. If you receive a request for information from any other domain, please contact us directly at info@calyxoinc.com to verify the legitimacy of the communication.

We appreciate your interest in joining Calyxo and look forward to getting to know you through our official channels.