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The Study Start-Up Lead manages submissions and approvals for clinical studies, coordinates with various regulatory bodies, and ensures timelines meet global expectations.

The Clinical Trial Coordinator will assist in managing clinical trials, ensuring compliance, monitoring progress, and preparing study documentation.

As a Clinical Research Associate, you'll conduct site visits for clinical trials, ensuring compliance and data integrity, and collaborating with investigators.

Act as strategic liaison to investigator sites, build long-term relationships, support multiple studies, escalate operational issues, align site capabilities with study opportunities, monitor performance metrics, and drive site engagement and improvement initiatives.