Clinical Research Regulatory Coordinator I

Mass General Brigham

🏠 Remote
📍Boston, MA
Posted May 19, 2026

Job Overview

Position

Clinical Research Regulatory Coordinator I

Company

Mass General Brigham

Location

Boston, MA

Work Type

Remote

Job ID

li-4416673441

Job Description

Site: Mass General Brigham Incorporated

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
The Clinical Research Regulatory Coordinator I (CRRCI) works under general supervision to ensure the regulatory requirements for clinical trials are met. This position involves working with clinical teams, Institutional Review Boards (IRB), clinical trial sponsors and federal regulatory agencies. The CRRCI will be trained on the institutional and federal regulations governing clinical research. This position does not involve patient contact.

Principal Duties And Responsibilities
The following regulatory duties will be performed under general supervision by the Clinical Research Manager:

  • Maintain and organize study specific regulatory binders

  • Prepare and submit protocol amendments, continuing reviews, and safety reports to the IRB

  • Revise informed consent documents to include new risk information and/or updated protocol requirements through the course of the study

  • Manage adverse event and deviation/violation/exception documentation for all enrolled patients and report to the sponsor and IRB as required

  • Submit Data and Safety Monitoring Reports

  • Maintain source documentation of correspondence with the IRB, investigators, and sponsors throughout the clinical trial process

  • Collect, complete, and submit essential regulatory documents to various regulatory entities

  • Participate in monitoring visits and file all monitoring visit correspondence

  • Ensure appropriate documentation of delegation and training for all study staff members

  • Maintain screening and enrollment logs

Skills/Abilities/Competencies Required

  • Careful attention to detail

  • Good organizational skills

  • Ability to follow directions

  • Good communication skills

  • Computer literacy

  • Working knowledge of clinical research protocols

Qualifications
Education

Bachelor's Degree Related Field of Study required

Can this role accept experience in lieu of a degree?

Yes

Licenses and Credentials

Experience
Knowledge, Skills and Abilities

  • Careful attention to detail.

  • Good organizational skills.

  • Ability to follow directions.

  • Computer literacy.

  • Working knowledge of clinical research protocols.

Physical Requirements
Additional Job Details (if applicable)

  • Standing Occasionally (3-33%)

  • Walking Occasionally (3-33%)

  • Sitting Constantly (67-100%)

  • Lifting Occasionally (3-33%) 20lbs - 35lbs

  • Carrying Occasionally (3-33%) 20lbs - 35lbs

  • Pushing Rarely (Less than 2%)

  • Pulling Rarely (Less than 2%)

  • Climbing Rarely (Less than 2%)

  • Balancing Occasionally (3-33%)

  • Stooping Occasionally (3-33%)

  • Kneeling Rarely (Less than 2%)

  • Crouching Rarely (Less than 2%)

  • Crawling Rarely (Less than 2%)

  • Reaching Occasionally (3-33%)

  • Gross Manipulation (Handling) Constantly (67-100%)

  • Fine Manipulation (Fingering) Frequently (34-66%)

  • Feeling Constantly (67-100%)

  • Foot Use Rarely (Less than 2%)

  • Vision - Far Constantly (67-100%)

  • Vision - Near Constantly (67-100%)

  • Talking Constantly (67-100%)

  • Hearing Constantly (67-100%)

Remote Type
Remote

Work Location
101 Merrimac Street

Scheduled Weekly Hours
40

Employee Type
Regular

Work Shift
Day (United States of America)

Pay Range
$20.16 - $29.01/Hourly

Grade
5

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 opportunities, differentials, premiums and bonuses as applicable and recognition programs designed to celebrate your contributions and support your professional growth. We invite you to apply, and our Talent Acquisition team will provide an overview of your potential compensation and benefits package.

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 at (857)-282-7642.

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.

Interview Prep

AI-powered insights to help you prepare

Key Skills

Required:
Preferred:

Practice Questions

💡Technical Questions (3)
  • 1.Can you walk me through the steps you would take to prepare and submit a continuing review to the IRB?
  • 2.How would you manage the documentation for an adverse event that must be reported to both the sponsor and the IRB?
  • 3.If a protocol amendment requires updates to the informed consent document, what is your process for ensuring the revised form is properly implemented?
🎯Behavioral Questions (3)
  • 1.Tell me about a time when your attention to detail prevented a significant error in a project or regulatory process.
  • 2.Describe a situation where you had to manage multiple competing deadlines from different stakeholders, such as sponsors, IRBs, and internal teams.
  • 3.Give an example of a time you had to follow strict directions or regulations that you found overly complex. How did you ensure compliance?
🧩Situational Questions (2)
  • 1.You discover that a study team member has been using an outdated, unapproved informed consent form for the past week. What do you do?
  • 2.A sponsor monitoring visit is scheduled for tomorrow, and you realize a key piece of regulatory documentation is missing from the binder. How do you handle this?

Resume Keywords

Make sure these keywords appear on your resume

IRB submissionsRegulatory bindersInformed consentAdverse eventsProtocol amendmentsContinuing reviewClinical trialsSource documentationMonitoring visitsSafety reportsDeviation reportingRegulatory compliance

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