Field Clinical Engineers play a critical role in bridging the gap between product innovation and real-world patient outcomes. This posting invites experienced clinical professionals to register their interest in future Field Clinical Engineer opportunities, where you could support the delivery of medical technologies in clinical settings while ensuring regulatory compliance and patient safety. Please note the content of this advert does not represent a live vacancy. About the opportunity This is an opportunity to register your interest in future Field Clinical Engineer positions within clinical trial support and field operations. Roles of this type typically sit at the intersection of clinical protocols, regulatory requirements, and healthcare delivery, working directly with clinical sites, hospitals, and trial coordinators to ensure that medical devices and technologies are implemented safely, effectively, and in full compliance with applicable regulations and data integrity standards. Typical role overview

Location:

Chicago, Illinois, USA Type:

Permanent

•

Full-time Salary:

$110,000 - $170,000 per annum, dependent on experience

Domain:

Clinical trial support

• medical device field operations

• healthcare compliance What you would do Typical responsibilities could include: Supporting the implementation and monitoring of medical devices and technologies within clinical trial environments Coordinating with clinical sites, hospital staff, and trial coordinators to ensure protocol adherence and proper device utilization Conducting on-site training and troubleshooting to support clinical teams and end users Documenting device performance, patient safety observations, and protocol compliance data Assisting with regulatory documentation, data collection, and audit trail maintenance Contributing to post-market surveillance activities and field performance assessments Maintaining detailed records to support data integrity and regulatory requirements Collaborating with cross-functional teams including clinical operations, regulatory affairs, and quality assurance What you could bring Most roles of this type require the following: Must-have 2-5 years of experience in clinical engineering, biomedical engineering, clinical trial support, or related field operations Bachelor's degree in Engineering, Biomedical Engineering, or a closely related discipline Solid understanding of clinical trial protocols, regulatory frameworks (FDA, GCP), and healthcare compliance standards Knowledge of medical device regulations and post-market requirements Strong communication skills with ability to work effectively with clinical staff and diverse stakeholder groups Ability to travel regularly to clinical sites as needed Authorization to work in the United States Nice-to-have Clinical engineering certification or relevant healthcare compliance certification Prior experience in clinical trial monitoring or device implementation Familiarity with electronic data capture (EDC) systems and regulatory tracking platforms Experience with ISO 13485 or similar quality management standards Master's degree in a related discipline What roles of this type could offer Most roles of this type offer the following, dependent on the industry and seniority of the role: Opportunity to directly support patient safety and clinical innovation Exposure to regulatory processes and healthcare compliance frameworks Professional development through clinical trial experience and field-based learning Collaboration with clinical sites, hospitals, and multidisciplinary healthcare teams Potential for career progression in clinical engineering or regulatory affairs Comprehensive benefits package including health insurance (medical, dental, vision), paid time off, 401(k) retirement plan, and flexible work arrangements where supported by role requirements About Specialist Staffing Group Specialist Staffing Group connects talented professionals with meaningful opportunities in clinical and life sciences. We partner with leading healthcare organizations, medical device companies, and clinical research institutions to build teams that advance patient outcomes and drive innovation. Our mission is to match experienced professionals with roles where their expertise creates measurable impact in regulated, patient-centered environments. How to register interest If you are interested in being added to our database to be considered for future opportunities, registering is quick and easy. No cover letter required. We will be in touch when we are instructed on these roles to discuss the next step in your career. Please note that the content of this advert does not represent a live vacancy or any guarantee of future vacancies, and by responding to this advert you agree to us adding your details to our database for future opportunities.