Instructor-led Training

Explore The Full ClinCapture Application

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  • Certified ClinCapture Training
  • Eight 2-hour sessions each month (10am to 12pm PST)
  • Certificates provided upon successful quiz completion
  • Free support for North American customers who complete all 8 modules

Module 1 – Introduction to ClinCapture

Locate training and support materials
Create and share a study in Studio
Add and manage subjects in EDC
Perform clinical data entry in EDC

Module 2 – Study Workflow

Manage and modify subject data
Manage discrepancies and queries
Source data verify (SDV) subject data
Utilize the Investigator Signature feature

Module 3 – Build Studio – eCRF Design and Management

Design Simple CRFs
Understand ClinCapture Datatypes
Clone CRFs and Fields from another study
Understand how to interpret basic Metadata

Module 4 – Build Studio - Advanced eCRFs and Publishing

Design complex CRFs
Perform calculations
Publish and revise CRFs
Configure Partial SDV

Module 5 – Study Config – Settings, Events, and Groups

Configure System Settings
Understand Study Specific Settings
Create and Configure Events
Use Groups for cohorts or treatment arms

Module 6 – Study Config –Rules, Sites, and Testing

Create and test data validation Rules
Create Sites
Prepare a test plan for UAT

 

Module 7 – Production Deploy and Management

Move a study from @build to Production
Perform data extracts
Prevent users from seeing specific CRFs
Manage live user issues

Module 8 – Closing and Archiving

Understand steps needed to lock the Database in ClinCapture
Prepare for Archiving

 

 

Eric Morrie

Eric Morrie

Director of Product Operations

Eric is currently managing customer support, professional services, and product roadmap. Prior to joining ClinCapture, he worked with Wincere, a bay area consulting company and CRO, providing systems consulting and managing clinical and statistical programming. He previously worked at Onyx Pharmaceuticals, Abbott Vascular, and Bausch + Lomb, providing process and technology implementation for clinical operations, data management, regulatory affairs, and global product safety. His experience in academic research and healthcare at the University of Rochester Medical Center utilized diverse technologies and specialized programming. He has worked in the healthcare, pharmaceutical, and medical device industry for over 20 years.

Maxine Pestonk

Maxine Pestonk

Senior Project Manager & ClinCapture Trainer

Maxine Pestronk has been in the clinical trial industry since 1993. Having worked for contract research organizations, EDC software vendors, and pharmaceutical and biotechnology companies, Maxine has an array of experiences in the field of Clinical Data Management. Many of Maxine’s years in the industry were in roles related to training of data managers, reengineering process for conducting studies using EDC systems, and demonstrating the usefulness of quality metric programs. Maxine has a Master of Science in Computer Information Systems, is a licensed and registered Dietitian (RD / LDN), and is proud to be a Certified Clinical Data Manager (CCDM®).