Sobre esta vaga de Senior Clinical Research Program Manager na Mass General Brigham
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.
Job Summary
This position will have dual reporting to the AMC Division of Allergy and Clinical Immunology (ACI) Division Director and the Manager of Finance & Research Administration and He/She will work closely with the Director of Clinical Research. The Senior Clinical Research Program/Project Manager plays a key role in coordinating the clinical research program administration. This includes overseeing research protocol management; supervising and training staff; supporting principal investigators with strategic planning, team organization, and grant preparation; coordinating materials transfers and data management/sharing; managing budgets and financial planning; and supporting conference and travel planning.The position manages key administrative HR functions such as hiring (in coordination with PIs), onboarding, and this role will evaluate and conduct the education and training program for the clinical research coordinators. The Senior clinical research program manager will be responsible for the day-to-day supervision of clinical research coordinators, including performance support and annual performance evaluations (pay changes, promotions, renewals). The manager also helps define study responsibilities and level of effort, oversees time tracking and project communication, and supports clinical trial billing activities. Serves as a resource to ACI MGB coordinators and Principal Investigators.
Qualifications
KEY ROLES AND RESPONSIBILITIES:
Project Management (Essential Functions)
- Project Lifecycle & Team Leadership: Oversee all administrative aspects of multiple active and pending Clinical research projects from inception to completion; define scope, goals, deliverables, and timelines while delegating tasks and managing study coordinators.
- Operational Oversight: Drive Clinical research trial projects by developing protocols with PI and coordinators, organizing meetings, and ensuring adherence to research protocols, data agreements, and quality standards across the portfolio.
- Financial & Resource Management: Execute and reconcile financial transactions (Check Requests, eBuy, Advarra) and industry-sponsored payments using MGB OnCore and Insight; oversee procurement and maintenance of study equipment.
- Regulatory & IRB Compliance: Manage Central and local IRB submissions, continuing reviews, protocol expiration dates, and timely reporting to prevent lapses; maintain expert knowledge of FDA/NIH guidelines, IND/IDE applications, and ClinicalTrials.gov requirements.
- Clinical Subject Management: Develop recruitment strategies, screen participants for suitability, and serve as the primary liaison between patients, families, and PIs; perform clinical tasks including phlebotomy and ECGs as required.
- Data Integrity & Coordination: Manage data/materials transfer agreements between collaborating institutions; develop data collection systems (CRFs) and perform rigorous validation and quality control.
- Audit & Site Readiness: Facilitate study monitoring and auditing visits with sponsors and third-party auditors; provide guidance to research teams on federal/state compliance and Good Clinical Practice (GCP). Appropriately documents and completes study close-outs and fund inactivation.
- Communications: Manage all protocol inquiries, participant correspondence, and regular reporting to Principal Investigators regarding trial progress.
Other Duties & Responsibilities:
Manage multi-site clinical studies, including site identification and feasibility, compliance assessment, and support for site contracting and agreement execution. Train site staff on study protocols and use of web-based data collection systems. Develop standard operating procedures and collaborate with investigators, clinicians, software developers, and laboratory personnel. Provide human research education at MGB institutions to groups of varying sizes, as assigned.
Can this role accept experience in lieu of a degree?
No
Experience
Research Related Experience 5-7 years required and Supervisory Experience 3-5 years preferred
SKILLS/ ABILITIES/ COMPETENCIES REQUIRED:
- Thorough knowledge of federal and institutional policies governing clinical research
- A broad understanding of Hospital practices and policies to assess and direct a wide range of practice issues
- Knowledge of clinical research protocols
- Strong interpersonal, communication, and organizational skills.
- Proficiency in Microsoft Office and related software; ability to learn new systems quickly. Oncore and clinical trials.gov
- Ability to handle confidential information and maintain professionalism.
- Detail-oriented, proactive, and adaptable to changing priorities.
- Ability to work independently and as part of a team.
Additional Job Details (if applicable)
Remote Type
Work Location
Scheduled Weekly Hours
Employee Type
Work Shift
Pay Range
$78,936.00 - $128,928.80/Annual
Grade
8
EEO Statement:
Mass General Brigham Competency Framework
At Mass General Brigham, our competency framework defines what effective leadership “looks like” by specifying which behaviors are most critical for successful performance at each job level. The framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. These competencies are used to evaluate performance, make hiring decisions, identify development needs, mobilize employees across our system, and establish a strong talent pipeline.
