We are seeking a Trial Coordinator to support the delivery of clinical research in the Boston, Massachusetts area. This role could involve managing patient recruitment, coordinating study protocols and ensuring regulatory compliance across ongoing trials—working at the intersection of clinical excellence, data integrity and patient safety. 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 Trial Coordinator positions within clinical research, roles that could support the advancement of patient-centered care through rigorous protocol execution and regulatory adherence. Roles of this type may sit within a collaborative clinical research environment where you would coordinate the day-to-day activities of active trials, liaise with study teams, and maintain the highest standards of data quality and patient safety. Typical role overview

Location:

Boston, Massachusetts, USA Type:

Contract •

Full-time Rate:

$400 - $480 per day

Domain:

Clinical research • Trial coordination • Regulatory compliance What you would do Typical responsibilities could include: Coordinating patient recruitment, screening and enrollment across assigned trials Managing study protocols and ensuring adherence to trial-specific requirements Maintaining accurate and complete trial documentation and regulatory records Supporting informed consent processes and patient safety monitoring Communicating with study team members, sites and regulatory bodies Collecting, organizing and verifying clinical trial data for accuracy and completeness Preparing reports and study status updates for project leadership Assisting with regulatory submissions and audit-readiness activities What you could bring Most roles of this type require the following: 2-5 years of experience in clinical research, clinical trial coordination or related healthcare settings Working knowledge of clinical trial protocols, Good Clinical Practice (GCP) and regulatory frameworks Familiarity with data integrity practices and electronic data capture (EDC) systems Strong organizational and communication skills, with attention to detail Bachelor's degree in Life Sciences, Biology, Chemistry or related field (or equivalent professional experience) Authorization to work in the United States Nice-to-have experience includes GCP certification, prior experience with FDA-regulated trials, or exposure to specific therapeutic areas such as oncology, cardiovascular or immunology. 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 clinical research and patient-centered care Exposure to regulatory processes and healthcare compliance frameworks Opportunities to develop expertise in trial management and data integrity Collaboration with experienced research teams and healthcare professionals Professional development and potential progression within clinical research Contract flexibility with a daily rate of $400 - $480, dependent on experience and qualifications About Specialist Staffing Group We connect talented professionals with clinical and life sciences organizations across the United States. Our focus is on supporting rigorous research, regulatory excellence and patient safety through skilled recruitment and professional staffing. 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.