This is an opportunity to register your interest in future Data Management Coordinator positions within clinical trial operations. Roles of this type could support the integrity and compliance of patient data across regulated research environments, helping to bring critical therapies to the patients who need them. Please note the content of this advert does not represent a live vacancy. About the opportunity Data Management Coordinator roles in clinical research involve ensuring the accuracy, completeness and regulatory compliance of clinical trial data from enrollment through database lock. These contract positions could be based in Boston, Massachusetts, and would typically sit within a collaborative clinical operations team, working closely with clinical monitors, quality assurance specialists and regulatory coordinators to maintain the highest standards of data integrity and patient safety. Typical role overview

Location:

Boston, Massachusetts, USA Type:

Contract

•

Full-time Rate:

$560-$800 per day, dependent on experience and expertise

Domain:

Clinical trial data management

• Regulatory compliance

• Patient safety What you would do Typical responsibilities could include: Managing the collection, validation and entry of clinical trial data according to study protocols and regulatory requirements Performing data quality checks and discrepancy resolution to ensure accuracy and completeness Maintaining compliance with

ICH-GCP, FDA

regulations and company standard operating procedures Coordinating with clinical sites, monitors and study teams to resolve data queries and issues Preparing data for database lock and supporting statistical analysis readiness Documenting all data management activities and maintaining audit trails Supporting regulatory submissions and inspections with data integrity evidence Contributing to process improvements in data workflows and system efficiency What you could bring Most roles of this type require the following: Must-have 2-5 years of experience in clinical data management, clinical trial coordination or related healthcare data environments Bachelor's degree in Life Sciences, Data Science, Health Sciences or related field Working knowledge of ICH-GCP guidelines, FDA regulations and 21 CFR Part 11 Proficiency in electronic data capture (EDC) systems and clinical trial management platforms Strong attention to detail, with demonstrated ability to identify and resolve data discrepancies Excellent communication and organizational skills Authorization to work in the United States Nice-to-have GCP or clinical data management certification Experience with SAS or other statistical analysis tools Familiarity with CDISC standards Previous exposure to regulatory inspections 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: Hands-on involvement in advancing clinical research and contributing to patient safety Exposure to regulatory and quality processes that shape healthcare compliance Opportunity to develop technical skills in EDC systems, data analysis and regulatory knowledge Collaborative work environment with experienced clinical and operations teams Flexible contract terms and potential for extension based on project needs Professional development support in data management practices and clinical research standards About Specialist Staffing Group We are a specialized recruitment firm focused on connecting talented professionals with opportunities in clinical research, life sciences and healthcare. Our mission is to build strong partnerships between candidates and organizations, ensuring the right fit for both parties. We work closely with leading clinical research organizations, biotech companies and healthcare systems to identify and place skilled professionals who are passionate about advancing patient care and scientific excellence. 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.