Senior Study Monitor

Site: The Brigham and Women's Hospital, Inc.

 

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

Summary
The Senior Study Monitor provides centralized oversight of study quality and compliance across up to 15 participating sites. This role ensures protocol adherence, data quality, and consistent operational standards throughout the study.
Primary Responsibilities
Conduct timely centralized monitoring of site performance and protocol adherence
Review documentation and data quality across participating sites using remote data capture (RDC)
Able to conduct site-visits for monitoring purposes as needed.
Identify trends, risks, or compliance issues and support corrective actions
Coordinate closely with the Senior Project Manager on study priorities, and adherence to IRB requirements and research Good Clinical Practices (GCP) guidelines.
Maintain monitoring documentation and reporting in accordance with sponsor and institutional standards
Escalate significant issues through defined governance channels

Travel and Work Environment

Travel is expected, including a mix of remote monitoring and periodic onsite visits
Onsite visits are conducted in compliance with Mass General Brigham institutional policies
Flexibility required to coordinate monitoring activities across multiple sites

Reporting and Collaboration

Works in close coordination with the Senior Project Manager and research administration team

Core Competencies (Workday‑Aligned)

Quality & Compliance Attention to Detail Analytical Thinking Communication
Collaboration / Relationship Management
Competent and knowledgeable not Institutional Review Board general policies and requirements
Competent and adheres to Research Good Clinical Practices (GCP)
Familiar with RDC (Remote Data Capture) for monitoring purposes
Familiar with EDC (Electronic Data Capture) databases and Electronic Medical Records (EMR) 

 

Education
Bachelor's Degree Related Field of Study required

Can this role accept experience in lieu of a degree?
Yes

Licenses and Credentials

Experience
Previous Clinical Research Experience 1-2 years required, 3-5 years preferred and Previous experience with monitoring 2-3 year preferred

Knowledge, Skills and Abilities
- Ability to work independently and as a team member.
- Strong attention to detail and organizational skills.
- Knowledge of clinical research protocols.
- Knowledge of data management programs.
- Computer literacy.
- Knowledge of clinical trials, research, and general medicine.

 

 

Hybrid

 

221 Longwood Avenue

 

40

 

Regular

 

Day (United States of America)

 

Pay Range

$50,502.40 - $82,014.40/Annual

 

Grade

6

 

At Mass General Brigham, we believe in recognizing and rewarding the unique value each team member brings to our organization. Our approach to determining base pay is comprehensive, and any offer extended will take into account your skills, relevant experience if applicable, education, certifications and other essential factors. The base pay information provided offers an estimate based on the minimum job qualifications; however, it does not encompass all elements contributing to your total compensation package. In addition to competitive base pay, we offer comprehensive benefits, career advancement opp