This training course provides a comprehensive overview of the essential elements of clinical trial management and the overall drug development process, using real case studies, and practical examples.
Du lundi 19 septembre 2016 au mercredi 21 septembre 2016
Paris - ile de france
This course is suited to those newly appointed to a clinical study management position, e.g. monitors and clinical research professionals with some basic experience in the field of clinical research, who need a broader understanding of the principles of clinical study management. It is also suited to those who interact with clinical trial managers (such as IT, Finance, PV, QA and CTAs) as well as those in an academic research setting who interface with industry.
Clinical Research Professionals including CRAs, IT staff, Data Managers, Clinical Study Managers, Quality Management.
After successful completion of the training course, participants will be able to plan, execute and manage a clinical study.
Learning objectives:
This course will provide a deep insight into strategies and tools to prepare launch and manage a clinical trial from protocol to final report.
Learning outcomes:
- The clinical research phases and basic concepts of study design.
- Clinical Trial start-up incl. Regulatory framework, Study planning, Budgeting.
- Clinical Trial Conduct incl. Vendor management, Performance metrics, Communication plans, Risk management, Quality Management, Safety reporting requirements.
- General data management, statistical evaluation process and requirements for final study report preparation.
Time: 6:00 am - 12:45 pm.
Category: Classes / Courses | Professional Training | Classes, Courses & Workshops.
Prices:
Standard: EUR 2025,
Industry Member: EUR 1870,
Academia/Charitable/Government/Non-Profit Member (Full Time): EUR 935,
Academia/Charitable/Government/Non-Profit Non-Member (Full Time): EUR 1090.
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