Clinical Trial Project Management

• Project management - tools, plans & documentation
• Managing the "people-business" - skills and methods
• Setting up a project - critical success factors
• Surveillance of a project - resources, budget & quality
• Project close-out - lessons learned & process improvement

Who should attend

Project management in clinical trials is complex. A project manager must possess extensive technical knowledge to effectively oversee clinical studies from planning through to completion, as well as master the people skills necessary to ensure successful collaboration within the study team.

This seminar offers you both - specialized knowledge in project management of clinical drug trials as well as essential competencies for team management.

You will become familiar with the documents and measures that are used to steer and monitor clinical trials. You will understand the tasks assigned to you as a project manager during the various project stages of clinical trials. And you will learn how to ensure throughout the entire project duration that quality, data integrity, and budget compliance are maintained.

After the seminar, you will

• be familiar with the wide range of responsibilities associated with the role of a project manager in clinical drug trials.
• understand which documents need to be created, maintained, and monitored within the scope of project management.
• be capable of performing your practical tasks related to the planning, conduction, and surveillance of clinical trials.
• have gained an appreciation of the importance of aspects beyond purely technical PM-expertise, such as team leadership and communication.