Clinical Research Associates play a vital role in advancing therapeutic development by ensuring the integrity, compliance and safety of clinical trial data. This opportunity invites experienced research professionals to support Phase II-IV trials in a fast-paced, regulated environment where attention to detail directly impacts patient outcomes and regulatory success. 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 Associate positions within clinical trial coordination and site management. Roles of this type support the execution of multi-site clinical studies, working closely with investigators, sponsors and study teams to maintain protocol compliance, manage patient safety and ensure data integrity throughout the trial lifecycle. Typical role overview

Location:

Chicago, Illinois, USA Type:

Contract

•

Full-time Rate:

$400 - $480 per day

Domain:

Clinical trials

• life sciences

• regulatory compliance What you would do Typical responsibilities could include: Supporting protocol implementation and maintaining compliance with

ICH-GCP, FDA

regulations and institutional guidelines Coordinating patient recruitment, screening and enrollment activities, including informed consent procedures Managing study documentation, case report forms (CRFs) and regulatory files to ensure accuracy and completeness Monitoring adverse events and serious adverse events (SAEs), reporting to sponsors and IRBs within regulatory timelines Conducting site initiation meetings, staff training and ongoing communication with study sponsors Maintaining subject safety logs, pharmacy records and source document verification Preparing for regulatory inspections and managing audit responses Supporting data integrity through quality checks and issue resolution What you could bring Most roles of this type require the following: Must-have 2-5 years' experience as a Clinical Research Associate, Clinical Research Coordinator or equivalent trial support role Bachelor's degree in Life Sciences, Biology, Chemistry or a related field Knowledge of ICH-GCP guidelines, FDA regulations (21 CFR Part 11) and clinical trial protocols Familiarity with electronic data capture (EDC) systems and case report form (CRF) management Strong attention to detail, organizational skills and ability to manage multiple studies simultaneously Ability to communicate effectively with investigators, sponsors, patients and regulatory bodies Authorization to work in the United States Nice-to-have ACRP (Association of Clinical Research Professionals) or SOCRA certification Experience with Phase III or Phase IV trials Knowledge of specific therapeutic areas (oncology, cardiovascular, respiratory, etc.) Bilingual capability in clinical or healthcare settings 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 therapeutics that improve patient health and outcomes Exposure to regulated clinical trial environments and real-world healthcare systems Potential to develop specialized expertise in specific therapeutic areas or trial phases Professional development through ongoing training in GCP, protocol management and regulatory affairs Flexible work arrangements where supported by the role and sponsor requirements Opportunity to work with cross-functional teams spanning research, quality assurance and regulatory compliance About Specialist Staffing Group We are a leading recruitment partner specializing in clinical, life sciences and healthcare talent. Our mission is to connect qualified professionals with meaningful opportunities in regulated, patient-focused environments. We support clinical research organizations, sites, sponsors and healthcare providers across the United States, building teams that drive innovation and maintain the highest standards of patient safety and data integrity. 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.