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The Manager, Site Resourcing will oversee site management for clinical research, coordinate teams and budget, and ensure compliance with regulations.

As a Clinical Research Associate, you'll conduct clinical trial visits, ensure protocol compliance, manage data quality, and assist in study documentation.

Conduct site qualification, monitoring, and close-out visits for clinical trials while ensuring compliance and data integrity. Collaborate with investigators and prepare study documentation.

The Principal Biostatistician leads Phase I-III clinical trials, overseeing statistical activities and mentoring junior statisticians while engaging with clients and regulatory agencies.