Clinical trial management requires precision, expertise and unwavering commitment to patient safety. This publication invites experienced professionals to register their interest in future Specialized Trial Manager opportunities—roles that could position you at the center of bringing innovative treatments from development into clinical practice. 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 Specialized Trial Manager positions within clinical research and life sciences. Roles of this type support the design, execution and oversight of clinical trials under strict regulatory frameworks, contributing to the advancement of therapies that improve patient outcomes. Positions may sit within research organizations, contract research organizations (CROs), biotech firms or healthcare systems managing multi-site trials. The work could involve coordinating protocol compliance, ensuring data integrity, managing stakeholder relationships across sites and regulatory bodies, and maintaining vigilance over patient safety protocols throughout the trial lifecycle. Typical role overview

Location:

Chicago, Illinois, USA Type:

Permanent

•

Full-time Salary:

$90,000 - $140,000 per annum

Domain:

Clinical research

• regulatory compliance

• trial management What you would do Typical responsibilities could include: Managing end-to-end trial operations, from protocol initiation through closeout Coordinating multi-site trial activities and ensuring protocol adherence across all sites Overseeing regulatory submissions, ethics committee communications and compliance documentation Conducting site monitoring visits, monitoring for protocol deviations and managing corrective actions Maintaining comprehensive trial documentation and ensuring data integrity throughout the study Liaising with principal investigators, site coordinators, sponsors and regulatory agencies Tracking enrollment, safety data and key trial milestones Preparing and presenting trial status reports to internal and external stakeholders Identifying and mitigating trial risks and implementing solutions Supporting quality assurance processes and internal audit activities 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 a related life sciences role Bachelor's degree in Life Sciences, Biology, Chemistry or a related field Demonstrated expertise in clinical trial protocols and regulatory requirements (ICH-GCP, FDA, or equivalent) Working knowledge of data integrity, quality assurance and compliance standards Experience with electronic data capture (EDC) systems and trial management software Strong organizational, written and verbal communication skills Ability to manage complex, multi-stakeholder projects and timelines Authorization to work in the United States Nice-to-have Advanced degree (Master's or PhD) in Life Sciences or related field Certification as a Clinical Research Associate (CRA) or Clinical Trial Manager Experience with Phase II-IV trials in therapeutic areas such as oncology, cardiovascular, or immunology Familiarity with risk-based monitoring and adaptive trial designs 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 innovative treatments toward patients Engagement with cutting-edge clinical research methodologies and technologies Scope to lead trial operations and coordinate cross-functional teams Professional development through exposure to regulatory processes and global trial standards Potential progression toward senior management or specialist advisory roles A collaborative environment with principal investigators, CRO partners and regulatory professionals Competitive compensation, professional development support, health insurance, paid time off and retirement benefits, where supplied in the role details About Specialist Staffing Group We are a leading staffing partner specializing in clinical, life sciences and healthcare recruitment. We connect experienced professionals with organizations advancing patient care and innovative treatment development. 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.