Clinical Trial Management

SRC's Expertise Introduction:
"At SRC, our Clinical Trial Management course is designed to empower you with the skills to lead and manage clinical trials from start to finish, ensuring regulatory compliance and study efficiency."

Course Introduction:
This course provides a comprehensive overview of the essential principles and practices involved in managing clinical trials, including protocol development, site management, and compliance with global regulations.

What We Teach:

• Protocol Development and Study Design: Learn how to create detailed clinical trial protocols and implement study designs that meet regulatory and ethical standards.

• Site and Sponsor Management: Understand the fundamentals of site selection, sponsor communication, and trial oversight to ensure smooth and effective project execution.

• Regulatory Compliance and Documentation: Master the regulatory frameworks and documentation procedures required for managing clinical trials across different regions.

• Data Management and Reporting: Gain practical experience in managing trial data, monitoring results, and preparing comprehensive reports for sponsors and regulatory authorities.

Learning Objectives:

• Clinical trial lifecycle

• Protocol creation

• Regulatory adherence

• Site management

• Data analysis

• Compliance reporting

FAQs:

What qualifications are required for the Clinical Trial Management course?
A background in life sciences or healthcare is beneficial but not mandatory.

How long is the course?
The course runs for one month with 20 sessions, each lasting one hour.

What career opportunities are available after completing this course?
Graduates can pursue roles such as Clinical Trial Manager, Project Manager, or Regulatory Affairs Specialist.

Is this course suitable for beginners?
Yes, the course is designed for both beginners and professionals looking to transition into clinical trial management.

Are there hands-on activities included?
Yes, the course includes practical assignments and case studies to provide real-world experience in clinical trial management.