Donna Sattler
About Donna Sattler
Donna Sattler is the Director and Head of Standards Operational Management at Bristol Myers Squibb and leads the Data Standards Committee at SGM Alliance. She has over 22 years of experience in data management and statistical programming roles, contributing significantly to clinical data standards and inclusivity initiatives.
Company
Donna Sattler is affiliated with multiple organizations in key roles. Currently, she serves as the Director, Head Standards Operational Management at Bristol Myers Squibb in New Jersey. Additionally, she holds the position of Lead, Data Standards Committee at SGM Alliance, based in Miami, Florida. Her roles include a blend of remote and on-site responsibilities emphasizing data standards and operational management.
Title
Donna's current titles reflect her significant expertise in data management and operational standards. As the Director, Head Standards Operational Management at Bristol Myers Squibb, she focuses on enhancing clinical data standards and ensuring compliance. In her role as Lead for the Data Standards Committee at SGM Alliance, she contributes to the development and harmonization of industry-wide data practices.
Education and Expertise
Donna has pursued extensive education in various fields of study. She holds an MBA from Ursinus College, and she studied for an MBA at Regis University. Additionally, she has SAS Certifications from Philadelphia University and a BFA in Fine Arts Photography from Kutztown University of Pennsylvania. Her educational background also includes Graphic Design studies at Temple University. With over 22 years of experience, Donna's expertise spans data management, statistical programming, and clinical trial standards.
Background
Donna Sattler has a diverse professional background, beginning her career as a SAS Programmer at Johnson & Johnson. Her career spans various roles, including Senior Specialist at Octagon Research Solutions, Clinical Programmer at INC Research, and Technical Project Manager at MaxisIT Inc. She also has significant experience as a Consultant and Clinical Data Standards Lead at Eli Lilly and DePuy Synthes. Her role as Associate Director at Bristol Myers Squibb highlighted her capability in clinical data standards before she advanced to her current positions.
Achievements
Donna co-leads the CDASH initiative, which focuses on standardizing data collection in clinical trials. She is also an active member of the SOGI working group, contributing to inclusive data standards. Additionally, she leads the Disability Advancement Working Group and serves on planning and academic committees for organizations such as CDISC, PharmaSUG, PhUSE, and DIA. Donna is a PROUD LGBTQIA+ ally, advocating for diversity and inclusion within the clinical research industry, and excels in identifying gaps in clinical trial processes for better CDISC harmonization.