Hematology Oncology, Vice Chair of Clinical Research

Mass General Brigham•Somerville, MA

8d•$200,000 - $500,000•Onsite

About The Position

The Vice Chair for Clinical Research is a key member of the hematology oncology leadership team, reporting directly to the Physician-in-Chief. This position is a critical leader of the clinical research enterprise. Working closely with the Senior Director of the clinical trials office, Division Chiefs, and program leaders, the Vice Chair will provide physician oversight of the clinical trial portfolio, infrastructure, and compliance. The Vice Chair for Clinical Research is responsible for advancing MGBCI’s clinical research mission by ensuring robust operational support, facilitating collaboration across programs, and fostering excellence in clinical trial design, execution, and dissemination of findings.

Requirements

Advanced degree (MD or equivalent) with 10+ years in clinical research including leading clinical trials.
Leadership experience in clinical trials and research administration.
Strong knowledge of FDA, NIH, and other regulatory requirements for clinical research.
Ability to collaborate effectively in a matrixed environment.
Exceptional leadership, communication, and organizational skills.

Responsibilities

Develop and implement strategic plans to expand and enhance the clinical research portfolio of MGBCI.
Ensure alignment of clinical research activities with the mission and strategic priorities of MGBCI.
Ensure close collaboration with the other member institutions of the Harvard Cancer Consortium (HCC) and enhance the mission of HCC.
In close collaboration with the disease programs and the clinical trials office, oversee the portfolio of clinical trials at MGBCI, including industry sponsored, investigator initiated, and cooperative group studies.
Collaborate closely with the clinical trials office to ensure compliance with regulatory requirements and ethical standards for clinical research.
Develop and monitor metrics for clinical trial implementation and conduct.
Manage and enhance clinical trial infrastructure, including processes and systems to enhance trial implementation and conduct across MGBCI sites.
Innovate to increase efficiencies of trial implementation and conduct while maintaining the highest standards of quality.
Serve as a liaison between program directors, investigators, clinical research staff, to facilitate collaboration.
Provide regular updates to the MGBCI leadership on the status, challenges, and achievements of clinical research programs.
Maintain adherence to FDA, NIH, and other regulatory standards for clinical trials.
Ensure proper participation on SRC, IRB, audit and other review panels.
In collaboration with the clinical trials office, manage budgets and finances for clinical research activities.
Identify opportunities to secure funding for new and ongoing clinical research programs.
Design and implement training programs for investigators, coordinators, and other research personnel.
Promote best practices in clinical trial design, conduct, and reporting.
Foster a culture of mentorship and professional development in clinical research.
Ensure data integrity, security, and compliance with institutional and regulatory standards.