Clinical Data Managers play a critical role in ensuring the integrity, accuracy and regulatory compliance of data in clinical trials. This is an opportunity to register your interest in future Clinical Data Manager positions that support the delivery of life-changing therapies to patients through rigorous data governance and protocol adherence. 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 research environment where attention to detail and regulatory knowledge directly impact patient safety and trial outcomes. The work could involve managing data workflows across multiple therapeutic areas, ensuring compliance with ICH-GCP guidelines and FDA regulations, and partnering with clinical teams to maintain the highest standards of data integrity throughout the trial lifecycle. Typical role overview

Location:

Chicago, Illinois, United States Type:

Contract

•

Full-time Rate:

$560 - $800 per day

Domain:

Clinical trial data management

• regulatory compliance What you would do Typical responsibilities could include: Managing data entry, validation and reconciliation across clinical trial databases Monitoring data quality and resolving discrepancies in accordance with protocol and regulatory standards Preparing and maintaining accurate case report forms (CRFs) and electronic data capture (EDC) systems Supporting regulatory inspections, audits and quality assurance reviews Collaborating with clinical teams, sponsors and contract research organizations (CROs) to ensure timely and accurate data collection Documenting data management activities and maintaining comprehensive audit trails Identifying and escalating data integrity issues to appropriate stakeholders What you could bring Most roles of this type require the following: Must-have 2-5 years of experience in clinical data management or a related data management role Working knowledge of ICH-GCP guidelines, FDA regulations and clinical trial protocols Proficiency with electronic data capture (EDC) systems and clinical database platforms Strong attention to detail and commitment to data integrity and patient safety Experience with case report forms (CRFs), data validation and quality assurance processes Bachelor's degree in Life Sciences, Data Science, or a related field Authorization to work in the United States Nice-to-have SOCRA, ACRP or equivalent clinical research certification Experience with SAS or other statistical analysis software Familiarity with CDISC standards (SDTM, ADaM) Experience in oncology, cardiovascular or other regulated therapeutic areas What roles of this type could offer Most roles of this type offer the following, dependent on the industry and seniority of the role: Involvement in clinical trials that advance therapeutic innovation and patient outcomes Exposure to diverse therapeutic areas and cutting-edge research methodologies Development of specialized expertise in regulatory compliance and data governance Potential for progression into senior data management, clinical operations, or regulatory affairs roles Collaborative work environment with clinical researchers, sponsors and global teams Contract flexibility with potential for extension or conversion based on performance and organizational need About Specialist Staffing Group We are a leading provider of specialized staffing solutions across clinical, life sciences and healthcare sectors. We partner with forward-thinking organizations to identify exceptional talent that drives innovation, maintains regulatory excellence and delivers measurable impact. Our mission is to connect skilled professionals with meaningful opportunities where their expertise directly contributes to advancing patient care and scientific progress. 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.