Placet Research Global Services

Latin Pla´cet: "It seems right; it is approved of."

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Training of Clinical Research Professionals 
We are offering training seminars designed to prepare students for the careers in the field of Clinical Research. The courses are designed for recent college graduates and clinical staff looking to expend their understanding of clinical trial principles, or career-changing professionals looking to advance into the field of Clinical Research industry. Some of the most demanded and lucrative careers are CRA (Clinical Research Associates), Data Managers positions and CRC (Clinical Research Coordinator).

 
Our 4 week class consists of 40 hours of instructor-led training combined with approximately 80 hours of self-study. It shows students how to apply the detailed "book knowledge" to real-world clinical trials, using practical, current based on real-life scenarios.

We also offer one day seminar onsite or on designated location custom tailored to clients requirements including webinars in different languages.

Clinical Research Associate/Clinical Research Coordinator
• Medical/Clinical Terminology *
• The Drug and Device Development Process *.
• Good Clinical Practices *.
• The Science of Clinical Trials Design.
• Clinical Trials Site Monitoring *
• Practical Clinical Statistics for Non-Statisticians *
• Document Preparation: Protocols, Reports, Summaries.
• Case Report Forms Development
• Clinical Project Management
• Devices: Regulatory Strategy and Marketing Pathways.
• Preparing for FDA Inspections and Conducting Sponsor Audits. *
• Development of Clinical SOPs (Standard Operating Procedures)
• Contracting with Contract Research Organizations (CROs)
• Drug Safety and Adverse Events Reporting *
 
Data Management
• Medical/Clinical Terminology *
• The Drug and Device Development Process *
• Good Clinical Practices *
• The Science of Clinical Trials Design
• Clinical Trials Site Monitoring I
• Practical Clinical Statistics for Non-Statisticians
• Database and Query Resolution. *
• Document Preparation: Protocols, Reports, Summaries and Case Report Forms Development *
• Devices: Regulatory Strategy and Marketing Pathways
• Development of Clinical SOPs (Standard Operating Procedures) * 
 
Clinical Project Management at Investigator’s site
• Medical/Clinical Terminology.
• The Drug and Device Development Process*.
• Good Clinical Practices. *
• The Science of Clinical Trials Design. *
• Clinical Trials Site Monitoring
• Practical Clinical Statistics for Non-Statisticians. *
• Document Preparation: Protocols, Reports, Summaries. *
• Case Report Forms Development
• Clinical Project Management *
• Devices: Regulatory Strategy and Marketing Pathways.
• Preparing for FDA Inspections and Conducting Sponsor Audits.
• Development of Clinical SOPs (Standard Operating Procedures)
• Contracting with Contract Research Organizations (CROs) *
 
* -- Required Classes