Versatile clinical research professional knowledgeable about coordinating patient information, laboratory samples and compliance documents for diverse clinical trials. Highly organized and thorough with good planning and problem-solving abilities. Certified in [Area].
Adverse Events: Common Terminology Criteria for Adverse Events (V5)
Assessment, Recording and Reporting of Adverse Events
Fundamentals of Clinical Research
Essential Documents
New user training- CORe and PDMS
OneConnect-for Research Study Team Members
International Conference on Harmonization (ICH) E6 Good Clinical Practice Guidelines
Protocol Writing Tips
Source documentation
Clinical Research audit program
Data management in clinical trials
FDA Audits
Clinical Research Audit Program
Introduction to Informed consent
Adverse Events: Common Terminology Criteria for Adverse Events (V5)
Assessment, Recording and Reporting of Adverse Events
Fundamentals of Clinical Research
Essential Documents
New user training- CORe and PDMS
OneConnect-for Research Study Team Members
International Conference on Harmonization (ICH) E6 Good Clinical Practice Guidelines
Protocol Writing Tips
Source documentation
Clinical Research audit program
Data management in clinical trials
FDA Audits
Clinical Research Audit Program
Introduction to Informed consent