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FREE Information Session - Data Quality in Clinical Research 2019


During this Information Session the instructors Denise Redkar-Brown and Farida Dabouz will introduce their course called "Data Quality in Clinical Research" and will allow interested CDM's to ask any questions regarding this course.


  • Instructor Information
  • Course Overview & Objectives
  • Course Structure, Pacing and Timelines
  • Course Platform and Tools
  • Registration Process
  • Certification and CEUs


  • Denise Redkar-Brown

    Denise Redkar-Brown is the Principal at Sunburst Clinical Solutions dedicated to consultation in the area of Clinical Data Management training and auditing capabilities. Her last assignment in the corporate area was as Director of Scientific Affairs, Data Management at Cetero Research in Fargo, North Dakota. She is also a frequent contributor to the GCDMP and chairs SCDM's sub-taskforce on Electronic Learning. Denise began her career as a Medical Technologist working in a hospital laboratory environment. She made the transition to the pharmaceutical industry, and after more than 20 years, she has held positions in basic and clinical research. She is published in the European Journal of Pharmacology for her work in Pharmacology while at AstraZeneca and contributed to the successful submission for Accolate®, the first leukotriene antagonist for asthma therapy as well as other drugs and vaccines. Her latest publication was in the Good Clinical Practices journal (GCPj) in 2008 describing the evolving role of Clinical Data Managers.

  • Farida Dabouz

    Farida Dabouz, PhD. CCRP, is the president of FB2D Clinical Research Consulting Inc., a consulting company.
    Over the course of her multi-faceted 23 year career, she has worked in international pharmaceutical companies, CROs as well as academic international oncology group, in Europe and Canada. She has experience in the field of biostatistics, data management and medical writing as well as process improvement (quality assurance), applied in a vast array of therapeutics areas from Phase II to Phase IV, and observational studies.

    Dr. Dabouz has a strong experience in training investigators, study coordinators, nurses, project managers, CRAs, administrative assistants, QA and data managers, IT, as well as statisticians covering all data aspects, mainly demystifying statistics in clinical trials.

    Dr; Dabouz has a PhD in statistics and certified SOCRA. This certification allows being closer to clinical sites and working with investigators’ teams in improving data quality/integrity at the source.

August 22, 2019
Thu 8:00 AM PDT

Duration 0H 30M

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