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Clinical Research Engineer Jobs (NOW HIRING)

Clinical Research Coordinator We are seeking a dedicated Clinical Research Coordinator to join our ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

Clinical Research Coordinator We are seeking a dedicated Clinical Research Coordinator to join our ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

*URGENT NEED - Clinical Research Coordinator - MUST HAVE Oncology* Responsibilities * Lead and ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

*URGENT NEED - Clinical Research Coordinator - MUST HAVE Oncology* Responsibilities * Lead and ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

Clinical Research Coordinator - Dallas We are seeking a dedicated and skilled Clinical Research ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

... edc, clinical research coordinator, ivrs, epic, gcp, citi, medidata rave, sae, adverse event ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

Research Engineer

Los Angeles, CA · On-site

$89K - $99K/yr

... clinical, psychological and genotypic information with neuroimaging phenotypes for research ... Master's Degree in Electrical Engineering/Biomedical Engineering/Computer Science/Data Science and ...

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Clinical Research Engineer information

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$37K

$106K

$142.5K

How much do clinical research engineer jobs pay per year?

As of Jul 17, 2026, the average yearly pay for clinical research engineer in the United States is $106,012.00, according to ZipRecruiter salary data. Most workers in this role earn between $104,000.00 and $104,000.00 per year, depending on experience, location, and employer.

What are the typical projects and daily responsibilities of a Clinical Research Engineer?

Clinical Research Engineers are usually involved in designing and supporting clinical trials for new medical devices or therapies, collaborating closely with clinicians, regulatory specialists, and product development teams. Daily tasks may include protocol development, data analysis, managing documentation for regulatory submissions, and troubleshooting technical issues in study devices. You might also participate in site visits, train clinical staff on device use, and ensure strict adherence to quality standards. This role offers a dynamic mix of hands-on technical work and clinical interaction, providing exposure to multiple facets of healthcare innovation.

What are the key skills and qualifications needed to thrive in the Clinical Research Engineer position, and why are they important?

A Clinical Research Engineer should possess a strong background in biomedical engineering, clinical research methodologies, and regulatory compliance, typically supported by a relevant degree. Familiarity with clinical trial management software, statistical analysis tools, and Good Clinical Practice (GCP) certification is often required. Excellent problem-solving abilities, teamwork, and strong communication skills are key soft attributes for success in this interdisciplinary role. These competencies ensure effective design, execution, and analysis of clinical studies, ultimately contributing to the safe and efficient advancement of medical technologies.

What does a Clinical Research Engineer do?

A Clinical Research Engineer designs, develops, and evaluates medical devices, equipment, and technologies used in clinical research and healthcare settings. They ensure compliance with regulatory standards, conduct testing and validation, and collaborate with clinicians and scientists to improve medical solutions. Their role bridges engineering and clinical research to enhance patient care and medical innovations.

More about Clinical Research Engineer jobs
What cities are hiring for Clinical Research Engineer jobs? Cities with the most Clinical Research Engineer job openings:
What states have the most Clinical Research Engineer jobs? States with the most job openings for Clinical Research Engineer jobs include:
Infographic showing various Clinical Research Engineer job openings in the United States as of July 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $106,012 per year, or $51 per hour.
Clinical Research Coordinator

Clinical Research Coordinator

University of California San Francisco

San Francisco, CA • On-site

$28.50 - $38/hr

Full-time

This job post has expired today. Applications are no longer accepted.


University Of California San Francisco rating

8.9

Company rating: 8.9 out of 10

Based on 6 frontline employees who took The Breakroom Quiz

32nd of 555 rated colleges and universities


Job description


The Clinical Research Coordinator will perform independently or with general direction at the fully operational journey level of the series to execute, manage, and coordinate research protocols, as directed by the Clinical Research Supervisor and/or Principal Investigator (PI); may coordinate the data collection and operations of several concurrent clinical research studies under the guidelines of research protocols, UCSF and regulating agency policies.
Incumbent's duties may include, but will not be limited to supporting the management and coordinating the tasks of single or multiple clinical research studies, depending on their size and complexity; act as intermediary between services and departments while overseeing data and specimen management; manage and report on study results; create, clean, update, and manage databases and comprehensive datasets and reports; coordinate staff work schedules, assist with training of Assistant CRCs, and assist Clinical Research Supervisor and/or PI with oversight of other research staff; manage Investigator's protocols in the Committee on Human Research online system, as well as renewals and modifications of protocol applications and the implementation of new studies; participate in the review and writing of protocols to ensure institutional review board approval within University compliance; help assure compliance with all relevant regulatory agencies; oversee study data integrity; implement and maintain periodic quality control procedures; interface with departments to obtain UCSF approval prior to study initiation; maintain all regulatory documents; report study progress to investigators; participate in any internal and external audits or reviews of study protocols; and perform other duties as assigned.
Department Description:
The mission of the UCSF Department of Surgery is threefold: to develop the next generation of leaders in surgery; to provide outstanding quality clinical care that is cost effective, yet compassionate; and to make significant advances in scientific knowledge and clinical practice through basic and clinical research. Care of patients is what attracted our faculty and residents to surgery, and it continues to be our main focus.
The Department is comprised of seven divisions: Adult Cardiothoracic Surgery, General Surgery, Pediatric Cardiothoracic Surgery, Pediatric Surgery, Plastic & Reconstructive Surgery, Transplant Surgery, and Vascular & Endovascular Surgery. Our surgeons provide care at locations throughout greater San Francisco.
Qualifications
  • HS graduation and sufficient experience and demonstrated skills to successfully perform the assigned duties and responsibilities; and/or equivalent experience/training.
  • Attention to detail; strong interpersonal skills; excellent, effective verbal and written communication skills to coordinate with subjects, team members, other departments and outside institutions; and the ability to multi-task in a fast-paced environment while working with a diverse subject population.
  • Ability to work well independently, complete projects in a timely manner, and prioritize multiple projects to ensure the completion of essential tasks by deadlines.

Preferred Qualifications:
  • Bachelor's degree
  • Fluency in the usage of Committee of Human Research (CHR) online iMEDris system for submission, renewal, and modification of protocols through this system.
  • Understanding of patient population to create rapport and a relationship, while also giving insight to what is realistic and appropriate for patient participation.
  • Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals
  • Experience with electronic medical records.
  • Knowledge of UCSF and departmental policies for dealing with reimbursement, guidelines for research, confidentiality and HIPPA regulations, following the UCSF mission statement and purpose for research, and a clear understanding of policies and procedures on patient safety and confidentiality (electronic and hard copy medical records, patient charts, communication, etc.); knowledge of medical terminology, research policies and guidelines, guidelines for packing/shipping infectious substances, database building/analysis, and data management within some of the following: Access, Stata, SASS/ SPSS, and Teleform programming platforms.
  • Experience applying the following regulations and guidelines:
    • Good Clinical Practice Guidelines
    • Health Information and Accountability Act (HIPAA)
    • The Protection of Human Research Subjects
    • CHR regulations for recruitment and consent of research subjects
    • Effective Cash Handling Procedures
    • Environmental Health and Safety Training
    • Fire Safety Training

About Us
About UCSF
The University of California, San Francisco (UCSF) is a leading university dedicated to promoting health worldwide through advanced biomedical research, graduate-level education in the life sciences and health professions, and excellence in patient care. It is the only campus in the 10-campus UC system dedicated exclusively to the health sciences. We bring together the world's leading experts in nearly every area of health. We are home to five Nobel laureates who have advanced the understanding of cancer, neurodegenerative diseases, aging and stem cells.
Pride Values
UCSF is a diverse community made of people with many skills and talents. We seek candidates whose work experience or community service has prepared them to contribute to our commitment to professionalism, respect, integrity, diversity and excellence - also known as our PRIDE values.
In addition to our PRIDE values, UCSF is committed to equity - both in how we deliver care as well as our workforce. We are committed to building a broadly diverse community, nurturing a culture that is welcoming and supportive, and engaging diverse ideas for the provision of culturally competent education, discovery, and patient care. Additional information about UCSF is available here.
Join us to find a rewarding career contributing to improving healthcare worldwide.
Equal Employment Opportunity
The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected status under state or federal law.
Salary Information
The final salary and offer components are subject to additional approvals based on UC policy.
Your placement within the salary range is dependent on a number of factors including your work experience and internal equity within this position classification at UCSF. For positions that are represented by a labor union, placement within the salary range will be guided by the rules in the collective bargaining agreement.
To learn more about the benefits of working at UCSF, including total compensation, please visit: https://ucnet.universityofcalifornia.edu/compensation-and-benefits/index.html

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