Standard Operating Procedure for Training Investigators and Site Staff in Clinical Research

Purpose

The purpose of this SOP is to establish the process for training investigators and site staff involved in clinical trials and clinical studies. This SOP ensures that investigators and site personnel are adequately trained on study procedures, protocols, and regulatory requirements to conduct the study efficiently and ethically.

Scope

This SOP applies to all personnel responsible for training investigators and site staff in clinical trials and clinical studies, including study sponsors, clinical research organizations (CROs), and site management organizations (SMOs).

Responsibilities

• Sponsor: Oversees the training process and provides necessary training materials and resources.
• Principal Investigator (PI): Ensures that all site staff receive appropriate training on the study protocol and procedures.
• Clinical Research Coordinators: Support the training process and act as a point of contact for site staff.
• Training Coordinator: Organizes and conducts training sessions for investigators and site staff.

Procedure

• Training Plan Development:
  • Develop a comprehensive training plan based on the study protocol and requirements.
  • Identify the training needs of investigators and site staff.
  • Determine the appropriate training methods (e.g., in-person, online, or self-paced learning).
• Training Materials Preparation:
  • Prepare training materials such as presentations, manuals, and guides based on the study protocol.
  • Ensure training materials are clear, concise, and up-to-date.
• Training Sessions:
  • Conduct training sessions for