What you will learn
- The fundamentals of clinical research project managements
- How to navigate the project environment (governance, regulations, guidelines, SOPs)
- Be able to create an overview, plan, organize and draw up a budget for your project
- How to identify and manage the project stakeholders, CRO, site management and sponsor
- How to plan the clinical trial (milestones, phases and activities)
- How to manage ‘the dynamic cycle of Project Risk Management’ (planning, identification, analyzing, planning risk response, monitoring and controlling)
- How to analyze and manage risks by identifying project critical paths and their value to making informed decisions (‘The Risk’ mindset)
- How to estimate resource requirements (time and costs)
What your company will get
- A professional who understands the fundamentals of clinical research project managements
- A professional who understands the project environment (regulations, guidelines, standard operation procedures (SOPs))
- A professional who is able to create overview, plan, organize and draw up a budget for your project in a clinical setting
- A professional who can identify and manage the stakeholders of a project - CRO, Site Management and Sponsor
- A professional who can plan a clinical trial (milestones, phases and activities)
- A professional who can provide valuable input to all other team members in Clinical Project Management
- A professional who can operate in a highly dynamic and changing environment