Expert Profile
Sarah Fowler Dixon
Education Specialist, Washington University
Sarah Fowler-Dixon, PhD, CIP is Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for human subject research which has served as a model for other institutions. She crafted budgets, policies, procedures, reporting, and training for the new program. She has initiated the planning, development, authorship and implementation of many human subjects research policies, practices, guidelines, submission and reviewer forms often working with state and federal authorities. She has provided consultation regarding ethical, federal, state, and institutional requirements for faculty and staff both in the design and execution of their projects and teaches research ethics and regulatory affairs and the fundamentals of research management to graduate and undergraduate students. More recently, she lead a task force in the development of the Community Engaged Research Program at Washington University. Dr. Fowler-Dixon has simultaneously served as an Independent Consultant, providing expertise and creating supplemental educational materials, including a copyrighted workbook. Prior to joining Washington University, Dr. Fowler-Dixon was the Educational Development and Learning Specialist for Saint Louis University serving on various committees to improve research, procedures, community outreach, and retention.
Trainings by Expert
What are Serious Adverse Events and How do I Handle These?
Category:
Clinical Research
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Life Sciences
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Roles and Responsibilities
New Part 11 Guidance for Clinical Trials: What This Means for You
Category:
Clinical Research
,
Clinical Trial Regulations
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Documentation and Policy Management
,
Lifescience process & Procedures
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
,
IT
Institutional Review Boards (IRBs): The Changing Landscape and the Effect on the Conduct of Clinical Research
Category:
Clinical Research
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Audits & Inspections
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Trial Design and Management
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Ethics, Fraud and Misconduct
,
Clinical Trial Regulations
,
Audit & Inspection-Role
,
Clinical Research Audit
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
Achieving Research Compliance Through Risk Assessment
Category:
Clinical Research
,
Risk Management
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GCP & Other Best Practices
,
Clinical Trial Regulations
,
Regulations & Guidances
,
Regulatory Affairs
Electronic Data Integrity in a GxP Environment: Managing the Data Lifecycle for Compliance
Category:
Clinical Research
,
Audits & Inspections
,
GCP & Other Best Practices
,
Clinical Trial Regulations
,
Audit & Inspection-Role
,
Clinical Research Audit
,
Life sciences QA/QC
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
,
QA/QC
Issues related to informed consent in clinical trials
Category:
Clinical Research
,
Audits & Inspections
,
GCP & Other Best Practices
,
HR
,
Clinical Trial Regulations
,
Audit & Inspection-Role
,
Clinical Research Audit
,
Life sciences QA/QC
,
Regulations & Guidances
,
Life Sciences
,
Regulatory Affairs
,
Documentation and Data Management
,
QA/QC
