Field Clinical Engineers are essential to the successful delivery of clinical trials and medical device implementations. This is an opportunity to register your interest in future Field Clinical Engineer roles that could directly support patient safety and regulatory compliance in healthcare settings. 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 supporting clinical trial protocols and medical device deployment across healthcare facilities. Roles of this type may involve collaborating with clinical teams, research coordinators and regulatory stakeholders to ensure data integrity, protocol adherence and patient safety throughout trial execution and device implementation. Typical role overview

Location:

Chicago, Illinois, United States Type:

Contract

•

Full-time Rate:

$560 - $800 per day, dependent on experience and assignment length

Domain:

Clinical trials

• medical device support

• healthcare compliance What you would do Typical responsibilities could include: Supporting clinical trial execution by ensuring protocol compliance and data integrity across trial sites Collaborating with clinical research teams to train staff on device operation, troubleshooting and regulatory requirements Conducting site assessments and risk evaluations to identify compliance gaps and patient safety concerns Documenting technical issues, adverse events and protocol deviations with attention to regulatory reporting standards Coordinating with regulatory, quality and clinical affairs teams to address technical or compliance questions Maintaining detailed records of device performance, maintenance activities and site communications Providing real-time technical support during device deployment, calibration and troubleshooting Contributing to the resolution of field issues that could impact trial integrity or patient outcomes What you could bring Most roles of this type require the following: Must-have 2-5 years of experience in clinical engineering, field support, biomedical engineering or clinical trial support Bachelor's degree in Engineering, Biomedical Engineering or equivalent hands-on technical experience Working knowledge of clinical trial protocols, GCP (Good Clinical Practice) and healthcare regulatory frameworks Understanding of medical device classification, FDA regulations and post-market surveillance Strong communication skills and ability to work collaboratively with clinical and non-technical stakeholders Attention to detail and commitment to data integrity and patient safety Authorization to work in the United States Nice-to-have Relevant certifications (AAMI, ECRI or clinical engineering specialty certifications) Experience with electronic data capture (EDC) systems or clinical trial management systems Prior experience supporting Class II or Class III medical devices Familiarity with ISO 13485 or GxP quality systems Experience in a contract or temporary assignment environment What roles of this type could offer Most roles of this type offer the following, dependent on the industry and seniority of the role: Meaningful involvement in advancing clinical research and bringing new medical treatments to patients Direct exposure to regulated healthcare environments and real-world trial execution Potential to develop deeper expertise in clinical trial operations and medical device regulation Flexibility of contract-based work with opportunities to work across multiple trial sites and healthcare settings Professional development through exposure to diverse clinical protocols and therapeutic areas Collaborative work with experienced clinical research professionals and regulatory specialists About Specialist Staffing Group Specialist Staffing Group connects talented professionals with rewarding opportunities in clinical research, medical device support and healthcare innovation. We partner with leading healthcare organizations, contract research organizations (CROs) and device manufacturers to build teams that advance patient outcomes and regulatory excellence. 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.