Clinical data management is central to advancing patient safety and therapeutic outcomes in regulated trials. This is an opportunity to register your interest in future Data Management Coordinator roles that could support the integrity, compliance and delivery of clinical trial programs. Please note the content of this advert does not represent a live vacancy. About the opportunity Roles of this type may sit within a collaborative clinical operations environment where data stewardship directly impacts patient safety and regulatory compliance. The work could involve coordinating data collection, validation and reporting across trial sites, ensuring adherence to protocol requirements, regulatory standards and data governance frameworks. You could be involved in supporting trials from initiation through database lock, with scope to contribute to quality assurance and process improvement. Typical role overview

Location:

Chicago, Illinois, United States Type:

Permanent

•

Full-time Salary:

$110,000 - $170,000 per year, dependent on experience

Domain:

Clinical data management

• regulatory compliance What you would do Typical responsibilities could include: Coordinating data entry, validation and quality assurance across clinical trial sites Preparing and maintaining electronic data capture (EDC) systems in line with protocol and regulatory requirements Supporting case report form (CRF) design and trial database configuration Monitoring data completeness, accuracy and consistency to ensure regulatory compliance Liaising with clinical sites, data managers and quality assurance teams to resolve data queries Contributing to audit trails, regulatory documentation and data governance processes Supporting database lock activities and assisting with regulatory submissions What you could bring Most roles of this type require the following: Must-have 2-5 years of experience in clinical data management, clinical trials or related healthcare data roles Working knowledge of clinical trial protocols, Good Clinical Practice (GCP) and FDA/ICH regulatory standards Proficiency with electronic data capture (EDC) systems and data management software Familiarity with data validation, quality assurance and audit trail documentation Bachelor's degree in Life Sciences, Data Science, Health Sciences or related field Strong organizational and attention-to-detail skills Authorization to work in the United States Nice-to-have ACRP or SOCRA certification in clinical research Experience with CDISC standards (SDTM, ADaM) Knowledge of statistical analysis software (SAS, R) Experience supporting regulatory submissions or audits 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 contribution to clinical trial integrity and patient safety outcomes Exposure to diverse therapeutic areas and trial complexity Structured learning in regulatory compliance, data governance and healthcare standards Professional development opportunities toward senior data management or specialized trial roles Competitive compensation, benefits including medical, dental and vision coverage, paid time off, 401(k) and flexible work arrangements About Specialist Staffing Group Specialist Staffing Group partners with organizations across clinical research, life sciences and healthcare to build teams that drive compliance, quality and innovation. We support professionals at every career stage to find roles where they can make meaningful contributions to patient outcomes and scientific advancement. 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.