Clinical Study Specialist
ICON · Cambridge, MA +2 more
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Role summary
This hybrid role supports clinical trial operations across multiple sites and regions, managing study documentation, coordinating meetings, and tracking site activities and enrollment progress. The position requires organizing reports, maintaining trial records, and communicating with investigator sites while ensuring compliance with regulatory requirements. A bachelor's degree and minimum two years of industry experience are required, along with proficiency in trial master files, case management systems, and Microsoft Office applications.
What they're looking for
- Bachelor's degree
- Minimum 2 years industry-related work experience
- Experience supporting global clinical trials across multiple regions
- Proficiency with TMF, CTMS, and SharePoint systems
- Strong written and verbal communication skills
- Informed Consent Form review experience
- Proficiency in PowerPoint and Excel
What you'll be doing
- Generate analyzable reports and metrics for clinical study leadership
- Coordinate study team meetings, prepare agendas and documentation
- Collate data for feasibility assessments and site selection reviews
- Review and maintain study documents including protocols and case report forms
- Track site activation, enrollment, and monitoring activities against project timelines
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.