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September 3, 2026

1:00 pm ET - 3:30 pm ET

Location:

hybrid

Meeting of The Research, Development, and Regulatory Roundtable (R3)

September 3, 2026 @ 1:00 pm – 3:30 pm

The Research, Development, and Regulatory Roundtable (R3) is a forum to discuss pre-competitive issues in drug and device development, regulatory oversight of clinical trials, and human subjects research. Meetings convene policymakers, legal counsel, academicians, industry representatives, and global regulators. The R3 is a cooperative endeavor coordinated by the MRCT Center and Ropes & Gray LLP.

This hybrid meeting is open to sponsors of the Research, Development, and Regulatory Roundtable.

Topic: TBD

For more information, please email at MRCT@BWH.HARVARD.EDU

Deliverables

Projects

Research, Development, and Regulatory Roundtable (R3)

September 8, 2026

10:00 am ET - 12:30 pm ET

Location:

What’s Mine Is Mine and What’s Yours Is Mine: Data Ownership and Sovereignty 

September 8, 2026 @ 10:00 am – 12:30 pm

Topic: What’s Mine Is Mine and What’s Yours Is Mine: Data Ownership and Sovereignty

This meeting is open to sponsors of the MRCT Center Bioethics Collaborative and select invited guests. For more information about the Bioethics Collaborative and how to become a sponsor, click here.

September 22, 2026

10:00 am ET - 11:00 am ET

Location:

Virtual Event

Childhood Cancer Academic-Industry Collaborative Platform Trials (C3PT): Toolkit Launch Webinar

September 22, 2026 @ 10:00 am – 11:00 am

Virtual Event

The MRCT Center, in collaboration with ITCC (Innovative Therapies for Children and Adolescents with Cancer), Blood Cancer United, and the Children’s Oncology Group, will launch the Childhood Cancer Academic-Industry Collaborative Platform Trials (C3PT) Position Narrative and Toolkit, guidance for those planning and delivering platform trials for pediatric oncology.

The toolkit release marks the culmination of a two-year multi-stakeholder effort. In October 2024, the MRCT Center convened a group of experts for a two-day workshop, “Advancing Pediatric Platform Trials: Streamlining Development, Maximizing Impact,” that examined platform trials across pediatric oncology, major depressive disorder, and multidrug-resistant tuberculosis. A July 2025 follow-on workshop focused specifically on pediatric oncology, developing an implementation framework for academic and industry platform studies.

The C3PT resource includes a range of tools that support the user in putting that framework into practice. The toolkit offerings guide the user in determining whether a platform trial is the right trial design, what the optimal timing is for sponsor and regulatory interactions, guidance on templated sections for PIPs and iPSPs, considerations related to intellectual property and contracting, operational planning, and funding models.

The webinar will include opening remarks, a moderated multi-stakeholder discussion, and audience Q&A.

Deliverables

Projects

September 24, 2026

12:00 pm ET - 1:00 pm ET

Location:

Investigator Oversight in Decentralized Trials: New Resources and Practical Tools

 

Webinar

September 24, 2026 @ 12:00 pm – 1:00 pm

The Investigator Oversight in Decentralized Trials project builds on the MRCT Center and Medable’s prior IRB/EC Considerations for DCT Review. As data capture and trial activities increasingly occur outside traditional trial sites, the characteristics of decentralized trial conduct have created uncertainty about Investigator oversight and how it should be structured when the PI has no supervisory or contractual role with others collecting data and conducting trial activities.

To help close that gap, the MRCT Center and Medable developed four new resources for investigator oversight in clinical trials with decentralized elements (DCTs), with input from the Investigator Oversight in DCT task force. These resources include a proportional oversight framework, an approach to optimize DCT elements, a model instruction sheet for local healthcare providers, and a set of illustrative scenarios covering roles and responsibilities in common clinical situations from withdrawal requests to serious adverse events.

On Thursday, September 24, 2026, from 12:00 PM – 1:00 PM ET, the MRCT Center and Medable will host a webinar to release the resources and walk through their intended use and how they fit together.

IRB/EC Considerations for DCT Review
Ethical Considerations for Decentralized Clinical Trials: Tools, Resources and Best Practices

Bioethics Collaborative

October 21, 2026

8:00 am ET - 2:00 pm ET

Location:

MRCT Center 2026 Annual Symposium

Meeting

October 21, 2026 @ 8:00 am – October 22, 2026 @ 2:00 pm

JOIN US! MRCT Center 2026 Annual Symposium

The MRCT Center 2026 Annual Symposium returns to Boston on Wednesday, October 21, 2026, to be held at the offices of Ropes & Gray in Boston. Join us for a full day of discussions and presentations on ethical, actionable, and practical solutions to today’s global clinical research challenges.

On Thursday, October 22, the MRCT Center leads a day dedicated to data sharing, co-organized with Vivli.

The symposium is hybrid, in-person in Boston, and online, and it is free and open to all. Registration is now open. Attend one day or both, in person or virtually. The keynote and full agenda will be announced in the coming weeks.

Register today to secure your spot and help drive responsible innovation in clinical trials.

AI in the Operations and Administration of Clinical Trials will be featured at the 2026 MRCT Center Annual Symposium.

As part of this effort, we request individuals and organizations to share pilots, tools, and/or technical solutions. Please contact Trevor Baker (tbaker13@bwh.harvard.edu) if you have or know of such solutions. In addition, please feel free to introduce us to others you know, or let us know of others to whom we should reach out.

Bioethics Collaborative

November 5, 2026

1:00 pm ET - 3:30 pm ET

Location:

hybrid

Meeting of The Research, Development, and Regulatory Roundtable (R3)

November 5, 2026 @ 1:00 pm – 3:30 pm

The Research, Development, and Regulatory Roundtable (R3) is a forum to discuss pre-competitive issues in drug and device development, regulatory oversight of clinical trials, and human subjects research. Meetings convene policymakers, legal counsel, academicians, industry representatives, and global regulators. The R3 is a cooperative endeavor coordinated by the MRCT Center and Ropes & Gray LLP.

This hybrid meeting is open to sponsors of the Research, Development, and Regulatory Roundtable.

Topic: TBD

For more information, please email at MRCT@BWH.HARVARD.EDU

Deliverables

Projects

Research, Development, and Regulatory Roundtable (R3)

December 1, 2026

11:00 am ET - 1:00 pm ET

Location:

Joint Task Force for Clinical Trial Competency (JTF) Global Biannual Meeting

Meeting

December 1, 2026 @ 11:00 am – 1:00 pm

The Joint Task Force for Clinical Trial Competency (JTF), anchored at the MRCT Center, develops and disseminates standards and practices for the global clinical research workforce. By fostering a cohesive and collaborative approach, the JTF ensures that professionals have the competencies to conduct clinical trials ethically and effectively.

Our international team of investigators, educators, and clinical research professionals has developed and/or utilizes a framework that defines the knowledge, skills, and attitudes necessary for conducting safe, ethical, and high-quality clinical research.

Join us on Tuesday, December 1, from 11:00 AM – 1:00 PM ET for the Joint Task Force for Clinical Trial Competency (JTF) Biannual Global Meeting. A detailed agenda will be posted in the coming months.

To learn more about the JTF Framework: https://mrctcenter.org/clinical-trial-competency/framework/overview/

All registrants will receive slides and a meeting summary after the meeting. This event is free.

Bioethics Collaborative

December 1, 2026

1:00 pm ET - 3:00 pm ET

Location:

Joint Task Force for Clinical Trial Competency (JTF) Global Biannual Meeting

Meeting

December 1, 2026 @ 1:00 pm – 3:00 pm

The Joint Task Force for Clinical Trial Competency (JTF), anchored at the MRCT Center, develops and disseminates standards and practices for the global clinical research workforce. By fostering a cohesive and collaborative approach, the JTF ensures that professionals have the competencies to conduct clinical trials ethically and effectively.

Our international team of investigators, educators, and clinical research professionals has developed and/or utilizes a framework that defines the knowledge, skills, and attitudes necessary for conducting safe, ethical, and high-quality clinical research.

Join us on December 1, 2026, 1:00-3:00 PM for the Joint Task Force for Clinical Trial Competency (JTF) Biannual Global Meeting to hear about global perspectives on implementing the JTF Framework. Updates include:

  • From Translation to Transformation: Advancing Clinical Research Competencies in Pakistan through the Urdu JTF Framework
  • Advancing Professional Standards and Recognition for Australian Clinical Trials Professionals
  • Professional Development of the Clinical Research Workforce in New Zealand Public Hospitals
  • Designing Experiential Learning with a focus on JTF Competencies at North Carolina Central University
  • Using JTF competencies in designing a master level training program in Clinical Data Science

To learn more about the JTF Framework: https://mrctcenter.org/clinical-trial-competency/framework/overview/

All registrants will receive slides and a meeting summary after the meeting. This event is free.

Bioethics Collaborative

December 8, 2026

10:00 am ET - 12:30 pm ET

Location:

Meeting of the Bioethics Collaborative

December 8, 2026 @ 10:00 am – 12:30 pm

Topic: TBD

This meeting is open to sponsors of the MRCT Center Bioethics Collaborative and select invited guests. For more information about the Bioethics Collaborative and how to become a sponsor, click here.