Clinical research specialists play a central role in ensuring that clinical trials meet rigorous regulatory standards while maintaining the highest standards of patient safety and data integrity. This is an opportunity to register your interest in future Clinical Research Specialist positions where you could contribute to advancing breakthrough therapies through meticulous trial management and compliance expertise. 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 Clinical Research Specialist roles within the life sciences sector, positions that could support the delivery of innovative therapeutic solutions to patients. Roles of this type typically sit within collaborative research environments where you could work across clinical operations, regulatory affairs and quality assurance to ensure that protocols are executed with precision and that patient safety remains paramount throughout trial cycles. Typical role overview

Location:

Chicago, Illinois, USA Type:

Permanent

•

Full-time Salary:

$90,000 - $140,000 per annum, dependent on experience

Domain:

Clinical research

• life sciences

• regulatory compliance What you would do Typical responsibilities could include: Managing day-to-day clinical trial operations, including protocol implementation and monitoring Ensuring compliance with FDA regulations, ICH-GCP guidelines and institutional review board (IRB) requirements Coordinating with principal investigators, research coordinators and sponsor companies to maintain trial integrity Reviewing and maintaining comprehensive trial documentation, including informed consent forms and case report forms Conducting site audits and quality assurance checks to verify adherence to protocol and regulatory standards Training and supporting research staff on trial procedures, data collection and patient safety protocols Managing adverse event reporting and escalation procedures in accordance with regulatory timelines Serving as a liaison between clinical sites and sponsor organizations on compliance and safety matters What you could bring Most roles of this type require the following: Must-have 10-15 years of experience in clinical research, trial management or clinical operations Bachelor's degree in Life Sciences, Biology, Chemistry or a related discipline Deep knowledge of FDA regulations, ICH-GCP guidelines and institutional review board processes Demonstrated expertise in protocol implementation, data integrity and regulatory compliance Strong documentation and record-keeping capabilities Excellent stakeholder management skills across clinical, regulatory and operational teams Authorization to work in the United States Nice-to-have Relevant certifications such as ACRP (Association of Clinical Research Professionals), SOCRA (Society of Clinical Research Associates) or equivalent Experience with electronic data capture (EDC) systems or clinical trial management software Knowledge of GCP audit procedures and quality oversight frameworks 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 contribute to clinical research that advances patient outcomes and therapeutic innovation Scope to develop expertise in emerging therapeutic areas and trial methodologies Potential for professional development through continuing education and regulatory training Structured progression aligned with clinical research career pathways Comprehensive benefits package including health insurance, paid time off, professional development support and flexible work arrangements where applicable About Specialist Staffing Group Specialist Staffing Group partners with organizations across the life sciences and healthcare sectors to connect experienced clinical research professionals with meaningful career opportunities. We understand the specialized knowledge and compliance expertise required in clinical research, and we are committed to supporting both candidates and employers in building high-performing teams dedicated to advancing patient safety and therapeutic innovation. 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.