Senior Clinical Research Program Manager

Mass General Brigham•Boston, MA

22h•$78,936 - $128,929•Hybrid

About The Position

Mass General Brigham relies on a wide range of professionals, including doctors, nurses, business people, tech experts, researchers, and systems analysts to advance our mission. As a not-for-profit, we support patient care, research, teaching, and community service, striving to provide exceptional care. We believe that high-performing teams drive groundbreaking medical discoveries and invite all applicants to join us and experience what it means to be part of Mass General Brigham. Working closely with the RII Division Chief, the Divisional Director of Epidemiology and Clinical Sciences Research, Divisional Principal Investigators (PIs), and in partnership with other RII Research Managers/Administrators, and reporting to the RII Senior Administrative Director, the Senior Clinical Research Program Manager provides high-level administrative support and operational oversight for the division's clinical trial portfolio. The Program Manager will be primarily responsible for guiding and mentoring clinical research personnel, with a dedicated focus on supporting junior principal investigators (PIs) and those navigating the clinical trial landscape. The position collaborates closely with the RII Clinical Operations/Program Director and Research Administrative Managers to ensure divisional clinical trials align with operational protocols, resource allocations, and institutional policies. Additionally, the Manager provides strategic leadership in research education and team development, overseeing a team of clinical research staff to ensure high-quality personnel management and professional growth.

Requirements

Bachelor's Degree Related Field of Study required
Research Related Experience 5-7 years required
Ability to effectively supervise and train Staff.
Excellent judgement and ability to interpret information and protocol.
Ability to make independent effective decisions.
Aptitude for technical problem solving.
Excellent organizational abilities to formulate and complete rigorous timetables.

Nice To Haves

Master's Degree Related Field of Study preferred
Supervisory Experience 3-5 years preferred

Responsibilities

Develops detailed protocol documents that meet federal institutional standards.
Ensures study design's compatibility with clinical practices.
Provides critical input as to feasibility of study design and available resources.
Ensures document consistency.
Responsible for developing/managing the clinical trial’s operating and capital budgets.