Project Management of Clinical Studies

Date : 7th June 2018 to 7th June 2018

Place : United States, Aurora

Website :https://bit.ly/2wQlQ2H

Contact Person:Training Doyens

Description:

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 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 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: https://bit.ly/2wOfBw8 Email: [email protected] Toll Free: +1-888-300-8494 Tel: +1-720-996-1616 Fax: +1-888-909-1882

Project Management of Clinical Studies will be held in Aurora,United States on date 2018-06-07

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Deadline for abstracts/proposals : 7th June 2018

Keynote Speakers : 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.

Venue :Training Doyens, Aurora, CO, United States

Check the event website for more details.