The therawis team is an experienced group of medical, clinical, and scientific professionalswith a track record of 20 years+ for each team member.
Medical Affairs
Clinical Affairs
Project Management
Clinical Trial Liaison
Pre-Launch and Launch Support
Medical Science Liaison
Support successful execution of clinical trials through close interaction with study sites to increase awareness and visibility in Europe
Develop, maintain and manage relationships with key opinion leaders and national coordinators
Provide background information to study protocol and the drug’s mechanism of action
Identify barriers of enrollment and develop strategies and recommendation of solutions to overcome these barriers site-specific and country-specific
Medical affairs
Provide support and response to medical questions within clinical trials, drug development and life cycle management
Provide consultancy for the establishment of clinical development plans
Create scientific training modules and materials
Write briefing packages to regulatory authorities such as FDA and EMA
Clinical Affairs
Project management of trials Phase 1-3
Ethical Committee (EC) and IRB submissions
Perform feasibility studies
Write study protocols and related documents
