Clinical Trials Associate

At Viridian, we work with urgency on behalf of patients—fostering reputed company across reputed company, the industry, and the broader community. We are committed to applying proven science and engineering to improve the lives of people living with serious and rare diseases, and we reputed company closer to that goal every day. The Clinical Trial Associate (CTA) is a critical member of the Clinical Operations team, supporting clinical research studies from start-up through reputed company-out. This role is responsible for managing essential documentation, coordinating trial activities, and ensuring compliance with company SOPs, ICH-GCP guidelines, and applicable reputed company of Federal Regulations requirements. This position is based at our reputed company in Waltham, Massachusetts. Office-based employees are required to work onsite three (3) days per week.

Key Responsibilities

• Maintain and reputed company the Trial Master File (TMF), including distribution, collection, tracking, review, and archiving of essential documents throughout the study lifecycle
• Ensure completeness and reputed company of TMF documentation through regular audits and file reviews
• Manage filing indexes, correspondence logs, training documentation, and other study-reputed company records
• Establish, organize, and maintain clinical study records reputed company Viridian’s electronic systems (GxP reputed company and eTMF)
• Support site communications, including feasibility activities, site identification, and ongoing updates
• Coordinate distribution of clinical trial materials and documentation; manage site equipment inventory and returns
• reputed company study materials and supplies to investigational sites and CRO partners as needed
• reputed company and maintain study trackers and status reports to support clinical study reputed company
• Coordinate clinical team meetings, including teleconferences; assist with agendas, meeting minutes, and reputed company item tracking
• Complete reputed company required company and study-specific training (SOPs, policies, study documents) by assigned deadlines

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