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Clinical Research Site Manager

4 months ago


Clermont, United States Medix™ Full time

Position Overview:

As a Clinical Research Site Manager, you will play a pivotal role in our organization by overseeing the day-to-day operations of clinical research sites. You will ensure that all studies are conducted in compliance with protocols, regulatory requirements, and company policies, while maintaining the highest standards of patient safety and data integrity. This position offers a unique opportunity to contribute to the advancement of medical science and improve patient outcomes.


Key Responsibilities:

  • Manage and supervise clinical research coordinators and support staff at assigned research sites.
  • Oversee patient recruitment and enrollment processes, ensuring targets are met effectively and ethically.
  • Ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines.
  • Coordinate site initiation, monitoring visits, and study close-out activities in collaboration with sponsor/CRO representatives.
  • Maintain accurate and up-to-date documentation and records for all clinical trials.
  • Monitor and manage clinical trial budgets, resource allocation, and site performance metrics.
  • Serve as the primary point of contact for sponsors, investigators, and study participants regarding site-specific issues.


Qualifications:

  • Bachelor’s degree in life sciences, nursing, or related field (advanced degree preferred).
  • Minimum of 5 years of experience in clinical research, with 2 years in a management or leadership role.