- Coordinate day-to-day operational activities supporting clinical trials and Rater Services programs.
- Support sites, clinicians, raters, CRAs, sponsors, and internal stakeholders with timely communication.
- Maintain study documentation, trackers, reports, and records, and manage communications and scheduling.
- Support study start-up, conduct, and close-out across Rater Training, Central Monitoring, Central Rating, and Scale Management.
- Monitor study progress and follow up on outstanding actions to help meet project timelines and deliverables.
- Assist with operational reporting, quality activities, and tracking deliverables against project requirements.
- Collaborate with Study Managers and functional teams to provide support across operational areas and changing priorities.
- Manage responsibilities in accordance with company SOPs, quality standards, and applicable regulatory requirements.
- Contribute to continuous process improvement and other operational activities as required.
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