Barbara Bierer

Professor

Brigham and Women's Hospital

United States

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Professor Barbara Bierer is a faculty member at Brigham and Women's Hospital in the United States. Her research centers on clinical trial enrollment policies, data retention standards in biomedical research, and the promotion of diversity and inclusion in clinical studies. Recent publications address the complexities of decision-making capacity in research participants and advocate for best practices in maintaining research integrity.

Articles (22)

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2022

Collaborators (3)

Leslie P. Francis

distinguished professor

University of Utah

UNITED STATES

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Annabelle South

University College London

UNITED KINGDOM

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Katie Gillies

MRC Senior Non-Clinical Fellow & Professor

University of Aberdeen

UNITED KINGDOM

View details

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Barbara Bierer

Research Interests

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About

Articles (22)

Disparate data retention standards in biomedical research

An Analysis of Institutional Review Board Policies for Enrollment of Adults with Impaired or Uncertain Decision-Making Capacity

Benefits that Offset Research Risks and Burdens are Qualitatively Different

Advocating for collaboration among key partners to promote diversity in clinical studies amid policy challenges in the United States of America

The roadmap to integrate diversity, equity, and inclusion in hematology clinical trials: an American Society of Hematology initiative

Analysis of the Choice of Control in Acupuncture Clinical Trials Involving Patients with Breast Cancer

Persistent exclusion of non-English speakers in Pediatric research: a national analysis using ClinicalTrials.gov

Assessing Federal Policies to Reduce Economic Barriers to Clinical Trial Enrollment

Defamation Claims Arising from Research Misconduct Cases: Best Practices for Institutions

Maintaining the Integrity of the Biomedical Research Record Through Timely, Appropriate Corrective Action

The Role of Institutional Review Boards in Improving the Inclusion of Sex and Gender as Variables in Clinical Research

The PubPeer conundrum: Administrative challenges in research misconduct proceedings

Site staff perspectives on communicating trial results to participants: Cost and feasibility results from the Show RESPECT cluster randomised, factorial, mixed-methods trial

Acknowledging Complexity and Reimagining IRBs: A Reply to Discussions of the Protection–Inclusion Dilemma

Review of diversity, equity, and inclusion by ethics committees: A Delphi consensus statement

Terms and conditions apply: an ethical analysis of mobile health user agreements in research

IRBs and the Protection-Inclusion Dilemma: Finding a Balance

Ensuring the Scientific Value and Feasibility of Clinical Trials: A Qualitative Interview Study

Engaging key stakeholders to overcome barriers to studying the quality of research ethics oversight

Characterization of key information sections in informed consent forms posted on ClinicalTrials.gov

Implementation of single IRB review for multisite human subjects research: Persistent challenges and possible solutions

Supported decision-making can advance clinical research participation for people with disabilities

Collaborators (3)

Leslie P. Francis

Annabelle South

Katie Gillies

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