Clinical Project Management

Module 1: Learn how to manage your clinical development project

  • 26. Nov 2018

3 days course

English

17.350,- DKK ex VAT
(app. 2.333,- EUR ex VAT)

module 1

Summary

Managing a clinical development project is a complex and intricate process. A trial has many factors to rely on to be executed successfully. Clinical Project Management Module 1 will strengthen your understanding of the methods you use when working on clinical development projects and the fundamental tools for planning and follow-up that maximize the efficiency and success of your project as well as your role and responsibilities as project manager.

During the course you will be able to create a project overview and plan, organize, allocate staff and draw up a budget for your project. You will become able to evaluate the collaboration in the project team and know how to deal with stakeholders.

As course participants will come from a wide variety of academia, CROs and pharma companies, network and exchange of experiences will be a big part of this module. We will do our best to take advantage of this by incorporating different experiences and viewpoints to the training sessions. The many practical exercises and discussions are great opportunities for you to strengthen your network.

Since this course is an interactive course with many cases and workshops that put the theoretical concepts into practice we expect you to participate actively.

This course is conducted in English and developed in collaboration with IMPLEMENT Learning Institute.
 

Keywords

Clinical project management
Generic project management toolbox (tools and techniques)
Project management methodologies
Clinical research methodologies
Clinical trial life cycle
Project timelines and budgets
Project risk management
Stakeholder management

What you will learn

  1. The fundamentals of clinical research project managements
  2. How to navigate the project environment (governance, regulations, guidelines, SOPs)
  3. Be able to create an overview, plan, organize and draw up a budget for your project
  4. How to identify and manage the project stakeholders, CRO, site management and sponsor
  5. How to plan the clinical trial (milestones, phases and activities)
  6. How to manage ‘the dynamic cycle of Project Risk Management’ (planning, identification, analyzing, planning risk response, monitoring and controlling)
  7. How to analyze and manage risks by identifying project critical paths and their value to making informed decisions (‘The Risk’ mindset)
  8. How to estimate resource requirements (time and costs)

What your company will get

  1. A professional who understands the fundamentals of clinical research project managements
  2. A professional who understands the project environment (regulations, guidelines, standard operation procedures (SOPs))
  3. A professional who is able to create overview, plan, organize and draw up a budget for your project in a clinical setting
  4. A professional who can identify and manage the stakeholders of a project - CRO, Site Management and Sponsor
  5. A professional who can plan a clinical trial (milestones, phases and activities)
  6. A professional who can provide valuable input to all other team members in Clinical Project Management
  7. A professional who can operate in a highly dynamic and changing environment
Available start dates

Registration quick facts

You can pay by credit card or by invoice. We charge the amount shortly after you register. If you cancel your registration more than 30 days prior to the course, you will receive a full refund. Read our cancellation policy.

Yes, if you experience any technical problems, please call us at + 45 39 27 60 60, or send us an email at contact@atriumcph.com

If you cancel your registration more than 30 days prior to the course, you will receive a full refund. If you get sick on the day of the course, you can hand over your seat to a colleague. To hand over your seat, please contact us at +45 39 27 60 60. Read our cancellation policy.

WANT TO KNOW MORE ABOUT THIS COURSE?

Contact Programme Director Gitte Hornemann Møller at +45 39 15 09 20

Send an email

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