Training programs
Clinical Team
01
- Clinical Trial Assistants
- Clinical Research Associates
- Clinical Leads
- Line Managers
Clinical Sites
02
- Clinical Site Start
- Clinical Site Advanced
Our Training Programs include:
Face-to-face trainings
LIVE Online programs with ZOOM technology
Exclusive training platform
An Exclusive Training Platform
Clinical Team Training
The Best CRAs Development Program
- 5 weeks
- 68 hours
- Training and Mentoring
- Certification
CRA Training
Clinical Team Enhancement
Monitoring Techniques
• The 7 responsibilities
•The 4 visits
• Quality Management
Solid Knowledge
• The foundation
• Clinical Research Associate Mindset
• How to handle study specific documents
Soft Skills
• The behavior that leverage performance
CRA Training
12 HOURS
Solid Knowledge
• Clinical research history
• Introduction of Evidence Based Medicine
• Good Clinical Practices
• Applicable regulatory requirements
• How to handle study specific documents
• CRA Mindset
• Introduction of Evidence Based Medicine
• Good Clinical Practices
• Applicable regulatory requirements
• How to handle study specific documents
• CRA Mindset
CRA Training
Monitoring Techniques
Take a look at our curriculum on monitoring techniques:
- Communication
- Site Resources
- Investigational Product
- Informed Consent
- Data Verirication and Safety
- Trial Master File
- Recruitment
- Site Selection Visit
- Site Initiation Visit
- Site Monitoring Visit
- Close Out Visit
- General Quality Management
- Audits
- Inspections
CRA Training
Soft Skills
The behavior that leverage performance.
What we teach about soft skills:
DISC Behaviour Analysis
- Web-Based assessment
- Individual Analysis for Self-Awareness and Active Development
Building Relationship
- With sites
- With sponsor
- With study team
Time Management
- Time Triad
- The cyclic method for CRAs
Negotiation
- Influence
- Relationship maintenance
- Tecniques
Results Orientation
- Company and Study Goals Clarity
- GROW Method
- Planning and Execution
- Time stealers and distractions
Communication
- Verbal and nonverbal communication
- Efficient Communication
LEARNING PATH
Learning Path:
Methodolgy
Active Learning based on practice:
- Theory, activities, simulations and role play
- Mastermind
- Exclusive tools
- Mentoring meetings and/or on-site
Certification
Certificated professionals after testing
- Tests based on case-studies
- Role-Play Test
- Site visit initiation and site visit
Learning Path
Solid Knowledge
Foundation for a strong, ethical and comprehensive execution and approach.
Technique and Soft Skills
Clinical Research Associates that are confident and efficient.
Strong Team
Clinical Research Associates that build trust with sites and represent the company brand.
Results
Customer satisfaction and sites engagement.
Our Exclusive Program
- The program can be 100% customized based on the actual needs
- Main relevant Standard Operational Procedures and Templates can be added to the program
- It can be adjusted for Clinical Trial Assistants
- Monthly individual or group mentoring meetings can be added to an extended support
- On-site and remote accompanied site visits with CRAs
Other programs
- The program can be 100% customized based on the actual needs
- Main relevant Standard Operational Procedures and Templates can be added to the program
- It can be adjusted for Clinical Trial Assistants
- Monthly individual or group mentoring meetings can be added to an extended support
- On-site and remote accompanied site visits with CRAs
Trained and Certified CRAs
Professionals ready to start working:
- Strong Foundation
- Monitoring Techniques
- Soft Skills
- Practice – 42 hours Internship
- Oversight after hiring for 2 months
Support on specific needs
- Clinical trials processes analysis and creation
- Recruitment planning based on patient Journey for clinical trials
- Synergy enhancement among departments
- Relationship plan with clinical sites
Quality Management and Control
Audit
CAPA
Process Improvement
Quality Maintenance
The Clinical Research Professional must honor the trust of participants and future patients in the scientific process.