Project Management of Clinical Studies
OVERVIEW
- State
of the industry
- Initiating
projects
- Planning
projects
- Resources
- Dates
- The
management of Phase I through Phase IV
- Executing
and controlling
- Risk
management and Quality Management
- Project
team dynamics
- Closing
Projects
WHY
SHOULD YOU ATTEND
This
online training course will focus on the basic principles of project managementand how they can be applied to best meet the needs of your clinical
trials. You will take away a set of project management skills and
techniques that can be immediately put to use.
This
is designed for biotechnology/pharmaceutical/medical device professionals who
are involved managing clinical trials and are looking to learn more about the
basic project management process and how it might apply to their tasks.
AREAS
COVERED
- The
Role of the Required Documentation
- The
Management of Dates and Resources
- The
use of Excel and MS Project
- The
Role of SOPs in the Preparation and Management of that Documentation.
- The
organization of Processes and Sub-Processes.
- How
to use Quality Management and Risk Management.
- The
Content and Format of SOPs.
LEARNING
OBJECTIVES
At
the conclusion of this course, participants should be able to:
- Define
clinical project management
- Plan
the work
- Estimating
Dates
- Produce
the schedule
- Work
in teams
- Forecast
a clinical trial budget
- Execute
and control the clinical plans
- Close
the project
WHO
WILL BENEFIT
- Project
Managers who manage Clinical Trials
- Financial
Staff
- Operation
managers and staff
- Auditors
- Compliance
Professionals
- Project
practitioners
- Quality
Assurance Professionals
For more detail please
click on this below link:
Email:
support@trainingdoyens.com
Toll Free: +1-888-300-8494
Tel: +1-720-996-1616
Fax:
+1-888-909-1882

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