Maintains project timelines in MS Project; distributes updates to the study team.
Schedules meetings; prepares agendas, takes minutes, files records.
Manages CTMS tasks: milestones, enrolment projections, helpdesk tickets.
Prepares and tracks study training; maintains training records.
Establishes study SharePoint site and manages access for team and sponsors.
Manages user access and study communications (SUSARs, newsletters, etc.).

🎯 Requirements

4-year college degree or equivalent in business/science/healthcare.
Minimum 2 years clinical trial support experience as CTA or similar.
Fluency in Microsoft Office (Outlook, Word, Excel, PowerPoint).
Strong customer service, teamwork and attention to detail.
Working knowledge of ICH-GCP, Precision SOPs, and regulatory guidance.
Excellent written and verbal communication in professional English.

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