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Who should attend?
This event will particularly benefit professionals involved in the planning, logistics, management and implementation of e-Clinical Trials. It will introduce new e-Clinical professionals to the entire scope of their responsibilities, and upgrade the knowledge base of experienced clinical supply professionals with new technologies and processes.
From pharmaceutical, biotech and CROs:
- Clinical Project Leaders
- Heads of Clinical Operations
- Heads of Clinical Research
- Clinical Research Associates
- Clinical Trials Managers
- Clinical/Site Monitors
- Regulatory Managers
- Clinical Auditors
- Heads of Quality Control/Assurance/GCP Compliance
- Clinical Statisticians
- Programmers
- Clinical Data Managers/Co-ordinators
- Clinical IT Managers
- Clinical/Medical Advisors
- Investigators
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Last year's attendees
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