Jefferson Health - Philadelphia, PA

posted 2 months ago

Full-time - Mid Level
Philadelphia, PA
10,001+ employees
Hospitals

About the position

The Clinical Trial Coordinator oversees the day-to-day activities of clinical trials, ensuring compliance with Good Clinical Research Practice (GCP) and applicable regulations. This role involves managing various aspects of clinical trials from startup to closeout, including protocol coordination, data management, and regulatory document preparation. The coordinator also trains and supervises research staff, maintains accurate documentation, and performs quality control assessments to ensure data integrity.

Responsibilities

  • Oversee the day-to-day activities of clinical trials in accordance with GCP.
  • Run portions of clinical trials from startup to closeout, including protocol coordination, feasibility planning, and data management.
  • Prepare and submit materials for the Institutional Review Board (IRB) and other regulatory bodies.
  • Maintain accurate subject logs and track expenses for clinical trials.
  • Perform regular quality control assessments to ensure compliance with GCP.
  • Organize and maintain documentation of all patient data.
  • Design electronic capture databases and manage collected data.
  • Assist in the orientation and training of new staff.
  • Develop workflows and revise SOP/guidance documents.

Requirements

  • High School Diploma or equivalent with 6 years of clinical research experience, or
  • Bachelor's degree with 2 years of clinical research experience, or
  • Master's Degree with 1 year of clinical research experience.
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