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As a Clinical Research Associate, you will monitor clinical trial sites, ensure compliance with protocols, and support site staff while managing multiple projects.

Lead one or more Clinical Data Science project teams, oversee project initiation, planning, and execution, and manage communication with clients and vendors. Four key responsibilities include quality control, issue tracking, project kick-off facilitation, and support in sales efforts.

The CRA will conduct clinical trial visits, ensure compliance, manage data quality, collaborate with site staff, and maintain audit readiness.

As a Study Start Up Specialist, you will conduct feasibility assessments, site identification and negotiations, ensuring compliance with regulations while driving study initiation success.