Mass General Brigham
Direct Workday career site

Senior Clinical Research Coordinator

Location
Boston-MA
Listed
Today

Site: The General Hospital Corporation

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 MGH CORE Program is seeking a full-time Senior Clinical Research Coordinator (CRC-Senior) to join our multidisciplinary team. This position offers the opportunity to take on a leadership role in advancing innovative supportive care research in oncology and palliative care. The MGH CORE Program brings together oncologists, palliative care specialists, psychiatrists, psychologists, nurses, and other allied clinician researchers dedicated to improving the quality of care and outcomes for patients and families facing cancer and serious illness.

Senior Clinical Research Coordinator (CRC)

The CRC-Senior will oversee program-wide regulatory and operational needs across multiple supportive care research studies. In addition to contributing to projects employing qualitative methods, survey data, and clinical trial designs, the CRC-Senior will help develop and implement standard operating procedures, onboard and train junior clinical research coordinators (CRCs), and ensure high-quality study execution and compliance. This position is ideal for candidates with prior research experience who are ready to take on supervisory and program development responsibilities.

Key Responsibilities

Leadership & Training

  • Train, and mentor entry-level CRCs, ensuring adherence to standard operating procedures and best practices.
  • Assist CORE faculty investigators with allocating workload and providing ongoing feedback.

Study Coordination

  • Provide an extra layer of support in managing CORE studies, including participant eligibility reviews, recruitment, informed consent, and coordination of study visits.
  • Assist with data collection (surveys, interviews, chart reviews) and quality control checks, using REDCap (Research Electronic Data Capture) or other programs.

Regulatory & Compliance

  • Prepare and maintain Institutional Review Board (IRB) protocol submissions, amendments, continuing reviews, and adverse event reports.
  • Ensure compliance with study protocols, Human Subjects and Good Clinical Practice guidelines, and institutional policies.

Program Development

  • Assist in developing standard operating procedures and quality assurance systems.
  • Contribute to creation of study templates and guidance for protocol design, database management, and grant submissions.

Additional Job Details (if applicable)

Education & Experience

  • Bachelor's degree required (health sciences, psychology, public health, nursing, or related field preferred)
  • Minimum of 2-5 years of post-baccalaureate research experience in clinical trials or human subjects research, including direct experience with IRB/regulatory documentation.

Skills & Competencies

  • Ability to oversee, train and evaluate others effectively.
  • Strong organizational, time management, and problem-solving skills.
  • Excellent interpersonal and written/verbal communication skills.
  • Ability to work independently and collaboratively across multiple investigators and teams.
  • Familiarity with REDCap and other data capture systems preferred.

Application Instructions

Please submit your resume and a cover letter (maximum 300 words) describing your background, interest in supportive care research, and what makes you a strong candidate for this leadership role. We value team members from diverse backgrounds and encourage applicants to share in their cover letter how their unique experiences, perspectives, or interests would contribute to our program's mission.

  • Remote Type
  • Onsite
  • Work Location
  • 125 Nashua Street
  • Scheduled Weekly Hours
  • 40
  • Employee Type
  • Regular
  • Work Shift
  • Day (United States of America)

Pay Range $26.78 - $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 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.

Read the original posting

From Mass General Brigham's careers page, first listed on Rolev.ai on November 13, 2026. Rolev.ai is not the employer.

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Common questions

Where is the Senior Clinical Research Coordinator job at Mass General Brigham located?

This Senior Clinical Research Coordinator position at Mass General Brigham is located in Boston-MA. Always check Mass General Brigham's application page for specific state eligibility or relocation policies.

How do I apply for the Senior Clinical Research Coordinator position at Mass General Brigham?

This listing links directly to Mass General Brigham's Workday application page. You can apply directly on Mass General Brigham's site, or use Rolev.ai to check your resume fit, generate a zero-hallucination tailored resume and cover letter for this posting, and autofill the Workday application form in 1 click with the Rolev.ai Chrome extension. You always review the form and press Submit yourself.