Job Description

IQVIA seeks a Site Manager to oversee clinical trial operations at a Jefferson City location. This role manages site staff, coordinates patient enrollment across multiple studies, ensures regulatory compliance, and serves as a clinical research coordinator on complex trials.

Responsibilities

• Oversee assigned site conduct; train staff and serve as point of contact for operations directors
• Develop and implement patient recruitment strategies to achieve enrollment targets across studies
• Serve as primary CRC on 6+ medium to high complexity studies and backup CRC as needed
• Maintain source documentation, perform quality control checks, and resolve data queries
• Coordinate study visits, obtain informed consent, report adverse events, and manage site-level compliance

Requirements

• Clinical skills experience obtaining vitals and performing procedures such as blood draws and EKGs
• Ability to fulfill CRC Level II responsibilities
• Extensive knowledge of GCP/ICH and applicable regulatory guidelines
• Superior knowledge of site operations and drug development processes
• Training in leadership, project management, and process development

Compensation: $64,600.00 - $161,500.00 base

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