Clinical Research Monitor

Site Monitoring Specialist

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

Conduct site monitoring visits in accordance with standards of practice guidelines and federal regulations to ensure that the rights and well-being of human subjects are protected and electronic case report forms (e-CRF) are accurate, complete, and verifiable from source documents. Essential Functions-Responsible for conducting study monitoring visits to assess protocol and regulatory compliance per the approved monitoring plan.

-Review and compare source documentation to CRFs to ensure data is complete and accurate.

-Draft site monitoring plans-Provide Investigator and study staff training at study initiation and as needed through the course of the trial-Review study-specific site documents, including regulatory documents, drug and device accountability logs, training logs, and delegation of authority logs.

-Maintain regular communication with assigned sites to support site enrollment, data entry, query resolution, and patient retention.

-Document site visit findings and observations via trip reports and letters.

-Escalate major visit findings as described in the monitoring plan to appropriate study team members.

-Prepare trip reports and follow-up letters; track issues to closure via CAPA where needed-Participate in weekly meetings with the study team.

Qualifications

Education

• Bachelor's Degree required; experience can be considered in lieu of a degree

Experience

• At least 1-2 years of clinical research experience required
• Previous experience with monitoring highly 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.

Additional Job Details (if applicable)

Working Conditions

• This is a hybrid role that requires an onsite presence at the office (325 Cambridge Street in Boston) 3x/week

Remote Type

Hybrid

Work Location

325 Cambridge Street

Scheduled Weekly Hours

40

Employee Type

Regular

Work Shift

Day (United States of America)

Pay Range

$50,502.40 - $82,014.40/Annual

EEO Statement:

0100 Mass General Brigham Incorporated is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religious creed, national origin, sex, age, gender identity, disability, sexual orientation, military service, genetic information, and/or other status protected under law. We will ensure that all individuals with a disability are provided a reasonable accommodation to participate in the job application or interview process, to perform essential job functions, and to receive other benefits and privileges of employment.

To ensure reasonable accommodation for individuals protected by Section 503 of the Rehabilitation Act of 1973, the Vietnam Veteran's Readjustment Act of 1974, and Title I of the Americans with Disabilities Act of 1990, applicants who require accommodation in the job application process may contact Human Resources.