Clinical Project Management Series II


14 - 16 April 2014, Singapore 9.00am - 5.00pm (Reg. from 8.30am)

Normal Course Fee: $2699 or $979 (One Day)
Early Bird Special: $2399 or $929 (One Day) (Before 8 Feb 2014)
Group (>3): $2264 or $899 (One Day)


Download Brochure Register Now Back to Course Listing



This is the Series II of the Advanced Clinical Project Management Topics comprising of 3 Single Day Topics. Clinical Project Management Series (I &II) for a complete view on this subject.

Series II Day One will cover the human resource management and Stakeholder/communication aspect of project management. Learn to plan project-specific training and ensure all team members are clear about their tasks, responsibilities and project deliverables. Keep the stakeholders aligned for maximum support for the project.

Series II Day Two Learn to build cost estimates with precision techniques. Understand Earned Value Management and Cost Control by EVM. Set up a budget for effective EVM cost control

Series II Day Three will bring you into details of developing two fundamental project documents: the Project Charter, and the Project Management Plan. Review the PMBoK TOC to better understand its structure, content, and how to work with it.

These training will combine both theory and practical with latest case studies and processes



  • Learn how to plan or adequate, project-specific training, how to ensure all project team members understand clearly their roles, tasks and responsibilities
  • Conduct Stakeholder analysis and understand what is needed to keep all these stakeholders aligned to support the project
  • Know how to effectively creating a budget for a clinical trial
  • Know how to control costs using EVM, including pass through costs
  • Understand the importance of risk management in controlling costs
  • Understand the role of the PM in cost control in any organizational structure
  • Develop the project documents: The Project Charter and the Project Management Plan.



  • Clinical Research professionals and associates
  • Clinical Scientist / Basic Scientist
  • Clinical Investigators / Principal Investigators
  • Experienced Clinical Quality Assurance Professionals
  • Project Managers
  • Clinical Study Coordinators
  • GCP-focused Regulatory Affairs Professionals



1 year of clinical trial management, or attend The Intensive “Essentials of Clinical Trial Management”



Mr Alexander Gissler
Principal Consultant, Director ProjectPharm Ltd.
(Mr) Alexander Gissler has over 20 years of experience in the pharmaceutical industry. Having joined the industry in 1992, he held various project management and senior management positions in different international site management and contract research organizations...Read More