Effective Project Management for Clinical Trials Videorecording

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Effective Project Management for Clinical Trials Videorecording

100% online

Training features

Fully online

no need to travel, just sit back, relax and enjoy the learning experience

On any device

you can log in via mobile, tablet or laptop

Flexible Schedule

start when you want and follow the course at your own pace

Continuous access

you will continue to have access to the course for 3 months after completing your registration

Conveniently designed video content

the course content is divided into shorter video lectures that will allow you to increase the attention span and improve the learning experience

Full slide deck

you will be able to download the full slide deck to support your learning

Certificate of completion

upon the completion of the course you will receive the certificate of completion signed by the course leader

Course description

Project Management of Clinical Trials requires more than having a good Project Manager. A Clinical Project Manager must have a thorough understanding of what is required for the clinical trial, the regulatory requirements, design implementation, technology, country cultures and medical practices is only the starting point. Understanding how to plan study start up to maximise study success. Managing CROs, Sponsors, laboratories, niche providers and technology require broad skills and knowledge.  This course will focus on honing the skills for excellent Clinical Project Management.

meet the training leader
Julianne Hull BSc MSc
Consultant and Trainer in Pharma Industry
United Kingdom
training

Brochure

Reveal the full schedule of the training as well as key topics, course objectives, key takeaways, special features, and the trainer bio!

Effective Project Management for Clinical Trials Videorecording online training organized by Fleming_Agenda Cover
key training

Topics

Project definition

Roles & responsibilities at different stakeholders and within your team

Optimization of protocol design

Critical to quality factors

Project risk analysis, issue management and CAPA

Prioritization during your clinical trials projects

Effective study feasibility

Study enrolment plan & patient recruitment challenges

Safety monitoring

Budget planning & management

Protocol adherence during crises

Inspection ready clinical trials

Management of vendors, CROs and subcontractors

Tracking timelines & measuring the progress of your projects

Project close out

Benefits of attending

In associate with

phetairos_logo

Phetairos is an associate community of world-class biopharmaceutical consultants and subject matter experts. We help our clients by using our combined experience and industry best practice to design and deliver innovative solutions across the entire biopharmaceutical value chain. Our independent “hands-on” approach helps our clients to release the full potential of their products, organisations & people. We are dedicated to consistent delivery of successful client outcomes through collaboration, quality assurance, flexibility, cultural alignment, transparency and knowledge sharing.

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