Overall Clinical Trials Process, Roles and Responsibilities

2 part webinar
60-minute presentation followed by 30-minute Q&A 

Presenter

Carol Antinori, Consultant, Data Management. Carol has been consulting for sanofi-aventis for the last 4 years and has a total of over 20 years of Data Management experience. She has worked in the Pharmaceutical, Biotech and CRO industries in a variety of therapeutic areas in all study phases.  

Overview

This program will provide an overview of the clinical trial process from study design through database lock and those roles, tasks and activities for which Clinical Data Managers assume responsibility. The roles and responsibilities will be defined to ensure clarity at the task and process level, as well as expected interactions and communication with the overall project team. 

Learning Outcomes

At the conclusion of the program the attendee will be able to:·        

  • Describe the clinical trial process from study design through database lock     
  • List roles and responsibilities for data management functions    
  • Describe the methods of managing processes and tasks 
  • Describe the expectations of communicating with the cross functional areas of the project team


Continuing Education Credit Opportunity                                        

Attendees are eligible for CEUs upon attendance and successful completion of assessment questions.  Each part of this 2 part webinar carries 0.2 CEUs.
SCDM is authorized by IACET to offer .2 CEUs for this program.