Clinical Engineering Specialists play a vital role in supporting clinical trials and medical device deployments, serving as the bridge between technology and patient safety. These professionals combine technical expertise with deep knowledge of regulatory requirements and healthcare compliance, ensuring that equipment, protocols, and data integrity meet the highest standards throughout the clinical lifecycle. 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 Clinical Engineering Specialist positions supporting clinical trial operations and medical device implementation in the Chicago area. Roles of this type may involve collaborating with clinical teams, regulatory affairs, quality assurance and operations to ensure seamless device deployment, protocol adherence, and patient safety compliance across trial sites or healthcare facilities. Typical role overview

Location:

Chicago, Illinois, USA Type:

Contract

Full-time Rate:

$560 - $800 per day

Domain:

Clinical engineering

• Medical devices
• Clinical trials
• Healthcare compliance What you would do Typical responsibilities could include: Supporting clinical trial setup and device deployment at trial sites or healthcare facilities Ensuring equipment meets regulatory standards and clinical trial protocols Collaborating with clinical teams to troubleshoot technical issues and maintain operational continuity Monitoring and documenting device performance, maintenance schedules and compliance metrics Assisting with regulatory documentation, audit preparation and quality assurance activities Training clinical staff on device operation, safety protocols and data collection procedures Maintaining detailed records to support data integrity and regulatory compliance Coordinating with engineering and quality teams to address protocol deviations or technical concerns What you could bring Most roles of this type require the following: 2-5 years of experience in clinical engineering, field service engineering, biomedical engineering or related healthcare technical field Demonstrated knowledge of clinical trial protocols, FDA regulations, GCP (Good Clinical Practice) and healthcare compliance standards Understanding of medical device design, functionality and regulatory pathways Strong troubleshooting and problem-solving skills in a regulated environment Excellent communication and documentation skills, with the ability to work effectively across clinical, regulatory and engineering teams Bachelor's degree in Engineering, Biomedical Engineering or equivalent professional experience Authorization to work in the

United States Nice-to-have:

Experience supporting Class II or Class III medical devices Familiarity with CDISC standards or electronic data capture (EDC) systems Relevant certifications (AAMI, CBET or equivalent) Experience in site monitoring or clinical operations What roles of this type could offer Most roles of this type offer the following, dependent on the industry and seniority of the role: Direct involvement in advancing clinical trials and bringing medical innovations to patients Exposure to cutting-edge medical device technology and clinical trial operations Opportunity to deepen expertise in regulatory compliance and healthcare standards Potential for contract extension or transition to permanent opportunities based on performance Collaborative work environment across clinical, engineering and quality functions Flexible scheduling arrangements where supported by the engagement About Specialist Staffing Group Specialist Staffing Group connects talented professionals with leading organizations across clinical, engineering, life sciences and healthcare sectors. We partner with industry leaders to build teams that drive innovation, ensure regulatory compliance, and ultimately support better patient outcomes. 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.