Job Description

IQVIA seeks a Site Manager to oversee clinical trial operations at an on-site location. The role involves managing study teams, coordinating patient recruitment, ensuring regulatory compliance, and supervising multiple concurrent trials across therapeutic areas.

Responsibilities

• Oversee assigned site operations; train staff and providers; serve as point of contact for operations leadership
• Coordinate enrollment and revenue strategies across multiple studies; develop and implement patient recruitment plans
• Serve as primary CRC on six or more medium-to-high complexity studies; back-up CRC support as needed
• Perform quality control on source documentation and regulatory materials; coordinate with Quality Assurance on process improvements
• Manage participant scheduling, informed consent, adverse event reporting, specimen handling, and study visit coordination

Requirements

• Clinical experience obtaining vitals, performing blood draws, EKGs, and similar procedures
• CRC Level II capabilities and demonstrated ability to fulfill those responsibilities
• Extensive knowledge of GCP/ICH guidelines and applicable regulatory requirements
• Superior experience with site operations and drug development processes
• Leadership, project management, and process development training

Compensation: $64,600–$161,500 base (annualized)

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