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LEAD DATA MANAGER: A CRITICAL ROLE IN ANY PROJECT OR TRIAL

Lead Data Manager: A Critical Role in any project or trial

2019

Overview 

Do you want to learn or enhance your skills and gain an understanding of the critical tasks managed by the Lead Data Manager (LDM)? This webinar will teach skills required to become a Lead Data Manager and the associated critical tasks that they perform, We will go over tools and techniques that are utilized to deliver on time and high quality data.
Join this SCDM Lead Data Manager: A Critical Role in any Project or Trial webinar. We will discuss best practices for developing and managing timelines, prioritizing and finalizing documentation, managing data review teams, cross-functional communications, define reporting needs, facing challenges, utilizing trainings and the efficiencies to be gained by using standards, work practices and SOPs.

What you'll learn 

The Attendee will:
  1. Learn how to develop and managing realistic timelines
  2. Understand techniques for timely completion of DM documentation
  3. Develop leadership skills needed to successfully manage DM review teams and interact with project team members
  4. Understand how to determine the appropriate level of reporting, Metrics/Status needed for a project
  5. Develop skills for handling challenges
  6. Realize efficiencies when utilizing standards, developing Work Practices and following SOPs

Who should attend 

Beginner and intermediate level.

What are the benefits 

This webinar will enhance skills for individuals in the Lead Data Manager role and will provide insight to best practices for those considering taking the leap into the role. It will also provide critical information for those who would like to understand the role and all associated benefits and complexities.

Meet the instructor 

Aina Horton
Manager, Clinical Data Management

Aina Horton is a Manager of data Management at UBC located in Blue Bell, PA with over 13 years of pharmaceutical industry experience. Aina provides experience in trial start up to trial database lock; providing assistance and guidance across all functional clinical groups (e.g. Programming, Biostatistics, Clinical, Quality Assurance, etc.). Aina has experience leading multiple clinical trials in Phase I-IV across therapeutic areas. Aina is a mentor and leader who provides study oversight and guidance to team members to be successful in their roles.

Earn CEUs

Participants are eligible to receive CEUs upon attendance and successful completion of a web-based assessment within 30 days after the webinar. CEUs are not granted after the 30-day assesment deadline.
SCDM is authorized by IACET to offer 0.2 CEUs for this program.

Webinar registration

Individual registration: $360 member / $420 non-member
Group registration (max.10 people per group): $960 member / $1140 non-member

Group Registration Policy: Any group registration allows up to 10 people to attend the webinar and to complete the webinar assessment. Credits will be granted on an individual basis upon successful completion of the assessment by the registered participants.