Best Practices for Project Management of Clinical Trials

Duration: 90 Minutes
This online training course will focus on the basic principles of project management and 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 in managing clinical trials and are looking to learn more about the basic project management process and how it might apply to their tasks.
Project Management of Clinical Trials
Product ID: 501532
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
Objectives of the Presentation
At the conclusion of this course, participants should be able to:
  • Define clinical project management
  • Plan the work
  • Estimate Dates
  • Produce the schedule
  • Work in teams
  • Forecast a clinical trial budget
  • Execute and control the clinical plans
  • Close the project
Why Should you Attend
With the increased amount of updated regulations, new technologies, and other healthcare changes most of these processes are undergoing changes that must be recognized and managed to maintain the Quality and Integrity of the products produced by these processes.

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
  • The responsibilities of the various stakeholders
Who can Benefit
  • Project Managers who manage Clinical Trials
  • Financial Staff
  • Operation managers and staff
  • Auditors
  • Compliance Professionals
  • Project practitioners
  • Quality Assurance Professionals
$375
Recorded Session for one participant
Get life time access with download option!
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  $500.00 Training CD
Free shipment within 4 Working Days of placing the order. Get life time access for unlimited participants.
  $600.00 Training USB Flash Drive
Free shipment within 4 Working Days of placing the order. Get life time access for unlimited participants.
For multiple location please contact our customer care team +1-510-857-5896.
How it works
Live Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • The webinar joining link, username and password for joining the webinar will be updated on your OCP Account 24 hours prior to the webinar
  • Presentation handouts in Downloadable PDF format will be updated on your OCP Account 24 hours prior to the live session
  • Login to the audio conference on the scheduled date and time
  • Get answers to your queries through interactive Q&A sessions via chat at the end of the session
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account 24 hours after the completion of the session
  • Please let us know your thoughts and views at the end of the webinar, your valuable feedback will help us improve
Recorded Session - How it works
  • Login to onlinecompliancepanel with your registered username and password https://www.onlinecompliancepanel.com/login
  • Upon purchase of the recorded session a link will be updated on your OCP Account within 24 hours
  • Please click on the link to access the Recorded Session
  • Presentation handouts in downloadable PDF format will be updated on your OCP Account within 24 hours of the purchase of the product
  • Download the Certificate of Attendance and Purchase Invoice from your OCP Account after 48 hours of the product Purchase
  • Please share your valuable Feedback at the end of the session
Instructor Profile:
Richard Chamberlain's experience includes consulting with numerous Pharmaceutical, Contract Research Organizations, and Medical Device companies in the areas of computerized project scheduling, strategic planning, Quality Management and Computer Systems Validation. He has also managed large-scale clinical projects including development of Remote Data Entry systems, Adverse Event reporting, Drug Supplies, project planning and supervision of staffs.

Apart from these Mr Chamberlain has taught numerous public and in-house courses on various aspects of Computer Systems Validation and Auditing Computer Systems; assisted in the development and validation of numerous computerized systems in all GxP environments; assisted with the development of all varieties of Standard Operating Procedures and other required documentation for Quality Management and Compliance to Regulations. He is also familiar with the various aspects of Computerized Systems and CFR 21, Part 11, FDA Guidelines for Computers, ICH-GCP, and GxPs.
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