Clinical research specialists play a crucial role in advancing medical science by managing the intricate details of clinical trials, ensuring patient safety, and maintaining the highest standards of data integrity throughout the research process. This opportunity invites experienced professionals to apply their expertise in regulatory compliance, protocol management, and healthcare operations within a dynamic, fast-paced clinical research environment. 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 Research Specialist roles within clinical trial management and life sciences research operations. Roles of this type typically support the delivery of critical clinical trials in Chicago, Illinois, working within a regulated healthcare environment where precision, compliance, and patient outcomes drive every decision. Typical role overview

Location:

Chicago, Illinois, United States Type:

Contract

•

Full-time Rate:

$640 - $880 per day

Domain:

Clinical Research

• Life Sciences

• Trial Management What you would do Typical responsibilities could include: Managing clinical trial protocols and ensuring adherence to ICH-GCP guidelines and FDA regulations Coordinating multi-site trial activities, including site initiation, monitoring, and closeout procedures Overseeing regulatory submissions and maintaining comprehensive trial documentation Ensuring patient safety through continuous monitoring of adverse events and protocol compliance Managing trial budgets, timelines, and resource allocation across study sites Collaborating with principal investigators, sponsors, and internal teams to resolve operational challenges Maintaining data integrity through rigorous quality control and audit procedures Training and supporting site staff on protocol requirements and regulatory expectations Preparing and delivering trial reports and regulatory submissions to relevant authorities What you could bring Most roles of this type require the following: 10-15 years of clinical research experience, with demonstrated expertise in trial management and regulatory compliance Bachelor's degree in Life Sciences, Biology, Chemistry or a related field; advanced degree preferred Advanced certification in clinical research (ACRP, SOCRA, or equivalent) or equivalent professional qualification Deep working knowledge of ICH-GCP guidelines, FDA regulations (21 CFR Parts 11, 50, 56, 312, 812) and healthcare compliance standards Proficiency with electronic data capture (EDC) systems and clinical trial management software Excellent written and verbal communication skills with ability to engage diverse stakeholders Strong organizational skills with demonstrated ability to manage multiple trials simultaneously Experience with study budgeting, financial tracking, and resource management Ability to work independently and as part of a collaborative team What roles of this type could offer Most roles of this type offer the following, dependent on the industry and seniority of the role: Contract-based flexibility with competitive daily rates reflecting extensive clinical research expertise Meaningful involvement in advancing treatments and therapies that directly impact patient outcomes Opportunity to work with leading clinical research organizations and pharmaceutical sponsors Professional development through exposure to diverse therapeutic areas and trial methodologies Collaboration with experienced investigators, regulatory specialists, and research coordinators Potential for contract renewal and progression based on performance and business needs Remote flexibility where applicable, balanced with on-site coordination requirements in Chicago About Specialist Staffing Group Specialist Staffing Group partners with leading clinical research organizations and life sciences companies to identify and place experienced professionals who drive innovation and maintain compliance in regulated healthcare environments. Our focus on clinical research, regulatory expertise, and healthcare operations enables us to connect skilled specialists with meaningful roles where their expertise directly contributes to advancing medical science and improving 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. 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.