Clinical Research Site Manager 244017 Job at Medix™, Hattiesburg, MS

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  • Medix™
  • Hattiesburg, MS

Job Description

The Clinical Research Site Manager is responsible for managing the day-to-day operations of a clinical trial site to ensure high-quality, compliant, and efficient execution of clinical studies. This role oversees site staff, coordinates with sponsors and CROs, ensures regulatory compliance, and supports patient recruitment and retention activities.

Key Responsibilities:

  • Manage site operations to ensure studies are conducted in compliance with protocols, GCP, and regulatory requirements
  • Supervise and support site personnel (e.g., study coordinators, nurses, and support staff)
  • Maintain essential regulatory documents and site files (ISF)
  • Act as primary liaison with sponsors, CROs, and monitors
  • Oversee and support patient recruitment, enrollment, and retention efforts
  • Ensure accurate and timely data entry and query resolution in EDC systems
  • Prepare for and support monitoring visits, audits, and inspections
  • Track study budgets, assist with contract execution, and manage site-related finances

Job Tags

Contract work,

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