Christina Mack Interview

Christina Mack, Ph.D., MSPH is Sr. Director of Epidemiology and Clinical Evidence in the IQVIA Real-World Insights division.

She is a recognized expert in effectiveness studies for medical devices and pharmaceutical products, sports injury research, and pharmacoepidemiology methods including the use of external comparators, propensity scores, instrumental variables, and missing data.  

Her work focuses on the use of electronic health record systems and claims data for research, with a focus in study design methodology, maternal health, orthopedics, oncology, and infectious disease.  

Dr. Mack oversees development of large evidence hubs and novel studies that augment primary data collection with existing data and leads the IQVIA Injury Surveillance and Analytics team which serves as the epidemiologic research arm of the NFL and NBA.

She is an epidemiologist and computer engineer by training, with Ph.D. and master’s degrees from the University of North Carolina at Chapel Hill and an engineering degree from the University of Notre Dame.  

Currently, Dr. Mack holds an academic appointment as Adjunct Assistant Professor of Epidemiology at the University of North Carolina at Chapel Hill and serves on the Advisory Board of the Carolina Health Informatics Program.

Dr. Mack has published manuscripts in leading journals and authored several chapters in the Agency for Healthcare Research and Quality (AHRQ) landmark publication “Registries for Evaluating Patient Outcomes: A User’s Guide” on the topics of designing registries for studies of medical devices, selection of data elements for observational research, missing data, and research networks.  

She is a speaker at regulatory, governmental, and academic forums on epidemiologic methods and novel study designs as well as careers in research.

Last but not the least, she has over fifteen years of scientific and technical experience working for Johnson & Johnson, GlaxoSmithKline, IBM, and the World Health Organization in addition to her work at IQVIA. Her regulatory experience includes advising the FDA, most recently as faculty at the 2017 MDEpiNet Annual Meeting and at the FDA Cardiac Research Safety Consortium discussing novel research methods and use of electronic medical records for outcomes trials.  

Please join me in welcoming Dr. Mack on the Clinical Trial Podcast.

This episode is brought to you by CBI Events.

The team at CBI has put together a Digital Therapeutics event in New York City on December 3-4, 2018. Topics range from strategies for new digital health projects to perspectives from the venture capital community on investment requirements for digital therapeutics.

Whether you’re a pioneer in this space or want to know just the right amount of information to get started, this event is going to value packed for you.

Some benefits from your participation in this event include:

  • Learning strategies on how to ensure data integrity
  • Understanding regulatory approaches to digital therapeutics and how to seamless approval in all regions
  • Finding out about payer approval requirements and uncovering changing business models
  • Collaborating with others on standard definitions and approaches to what constitutes a digital therapeutic
  • And much, much, more.

If you want to learn and network with others in the Digital Therapeutics space, you should attend the 2018 event in New York City on December 3-4, 2018. 

As a listener to this podcast, I’ve got an exclusive $500 discount to this event. When I mean exclusive, it really is exclusive. 

So head over to http://www.cbinet.com/digitaltherapeutics and use the code CTP500 at check-out to get your $500 discount. 

Register today to get your exclusive $500 off your event ticket using the code CTP500. This offer is only available to the Clinical Trial Podcast listeners.

Resources and organizations mentioned in this episode:

IQVIA

Food and Drug Administration (FDA)

Pubmed

ClinicalTrials.Gov

Norwegian Mother and Child Cohort Study (MoBa)

Global Fund

Clinton Foundation

World Health Organization and HIV

IBM

Johnson and Johnson

Organization of Eastern Caribbean Islands

Outcomes Sciences

MIT

Harvard School of Public Health

University of Lusaka

Quintiles

Healthcare Business Women’s Association

Agency for Healthcare Research and Quality (AHRQ) landmark publication “Registries for Evaluating Patient Outcomes: A User’s Guide” on the topics of designing registries for studies of medical devices, selection of data elements for observational research, missing data, and research networks

American College of Cardiology

National Cancer Institute

FDA’s Sentinel Initiative

NBA

NFL

MDEpinet

University of North Carolina Chapel Hill

New York Times

People mentioned in this episode:

Manuel Prado

Dr. Nancy Dreyer

Dr. Mark Travis

Rob Cahill

Leave a Reply

Your email address will not be published. Required fields are marked *