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Clinical Research Program Manager Jobs in Massachusetts

Clinical Research Manager

Boston, MA · On-site

$74K - $111K/yr

What You'll Do The Clinical Research Program Manager is the operational lead of the Coordinating Center for a multi-site Lyme disease research program spanning three regional hubs and more than 20 ...

What You'll Do The Clinical Research Program Manager is the operational lead of the Coordinating Center for a multi-site Lyme disease research program spanning three regional hubs and more than 20 ...

Research Program Manager

Boston, MA · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Research Program Manager, a DoD sponsored research position, is a Boston or Washington DC based position responsible for research program and project management spanning two recently awarded ...

Research Program Manager

Boston, MA

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

The Research Program Manager,a DoD sponsored research position, is a Boston or Washington DC based position responsible for research program and project management spanning two recently awarded ...

Partner closely with the Distributed Research Program Manager to prioritize initiatives, allocate ... clinical research operations, digital health research, UX research, or a related field. * 2+ years ...

$26.25 - $35/hr

The GI Oncology Clinical Research Program supports PI initiated, industry sponsored, and ... The CRC will be responsible for the primary data collection and management of patient clinical ...

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Showing results 1-20

Clinical Research Program Manager information

See Massachusetts salary details

$48.6K

$101.1K

$163.3K

How much do clinical research program manager jobs pay per year?

As of Aug 17, 2026, the average yearly pay for clinical research program manager in Massachusetts is $101,134.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,200.00 and $114,700.00 per year, depending on experience, location, and employer.

What does a clinical research program manager do?

A Clinical Research Program Manager oversees the planning, implementation, and management of clinical research studies within an organization. They coordinate research activities, ensure compliance with regulatory requirements, manage budgets, and supervise research staff. Their role is crucial in maintaining timelines, quality standards, and communication among stakeholders, including investigators, sponsors, and regulatory authorities. They also play a key part in developing study protocols and ensuring that research activities align with organizational goals.

What are the key skills and qualifications needed to thrive as a clinical research program manager?

To thrive as a Clinical Research Program Manager, you need a strong background in clinical research, project management, regulatory compliance, and often an advanced degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) platforms, and certifications such as CCRP or PMP are typically required. Excellent leadership, organizational, and communication skills set standout managers apart, enabling them to coordinate teams and stakeholders effectively. These skills and qualifications are crucial for ensuring clinical studies meet regulatory standards, stay on schedule, and achieve high-quality outcomes.

What are some typical challenges faced by clinical research program managers in coordinating multi-site studies?

Clinical Research Program Managers often encounter challenges when coordinating multi-site studies, such as ensuring consistent protocol adherence across locations, managing data collection timelines, and addressing site-specific regulatory requirements. Effective communication and strong organizational skills are essential to keep all teams aligned and to resolve issues promptly. Additionally, the role frequently involves collaborating with investigators, sponsors, and regulatory bodies to maintain study integrity and ensure compliance.

What is the difference between Clinical Research Program Manager vs Clinical Research Coordinator?

AspectClinical Research Program ManagerClinical Research Coordinator
CredentialsBachelor's or higher in life sciences, often with project management certificationsTypically holds a bachelor's degree in health sciences or related field
Work EnvironmentOversees multiple studies, manages teams, and coordinates with stakeholdersHandles daily study activities, patient interactions, and data collection
Employer & Industry UsagePharmaceutical companies, CROs, academic institutionsHospitals, clinics, research sites
Search & Comparison IntentFocuses on management, oversight, and program coordinationFocuses on study-specific tasks and patient management

The Clinical Research Program Manager oversees multiple research projects, manages teams, and ensures compliance across studies. In contrast, the Clinical Research Coordinator handles the day-to-day activities of individual studies, including patient interactions and data collection. Both roles require relevant credentials but differ in scope and responsibilities.

What are the most commonly searched types of Clinical Research Program jobs in Massachusetts?

The most popular types of Clinical Research Program jobs in Massachusetts are:

What are popular job titles related to Clinical Research Program Manager jobs in Massachusetts?

For Clinical Research Program Manager jobs in Massachusetts, the most frequently searched job titles are:

What cities in Massachusetts are hiring for Clinical Research Program Manager jobs?

Cities in Massachusetts with the most Clinical Research Program Manager job openings:

Infographic showing various Clinical Research Program Manager job openings in Massachusetts as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $101,134 per year, or $48.6 per hour.

Clinical Research Program Manager

Mass General Brigham

Boston, MA • On-site

$78K - $128K/yr

Full-time

Re-posted 2 days ago


Brigham and Women's Hospital rating

8.1

Company rating: 8.1 out of 10

Based on 101 frontline employees who took The Breakroom Quiz

121st of 1,060 rated hospitals


Job description

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
The Cancer and Well-being Research Program (CARE) at Brigham and Women's Hospital is
recruiting a full-time Clinical Research Program Manager to join its multidisciplinary team. The
program manager will work closely with the principal investigator in collaboration with a
diverse group of researchers (oncologists, palliative care clinicians, psychiatrists, psychologists)
to oversee the day-to-day administration of program activities. The program manager will
contribute to the development of study protocols and procedures, and the preparation and
submission of research manuscripts, abstracts, and grant applications. The program manager
will be responsible for hiring and onboarding new staff as well as maintaining a working
knowledge of clinical research conduct to support study-related activities and initiatives across
the program locally and nationally.
Qualifications
BA/BS degree required
• Minimum of 2 years of management experience required
Research and program responsibilities will include the following:
• Collaborate with the principal investigator to oversee all laboratory projects
• Work closely with the principal investigator on grant submissions, including summarizing
grant instructions and required elements, assisting with writing research proposals,
developing templates for required documents, and collecting required documentation
from investigators and study sites
• Assist with manuscript preparation for peer-reviewed journals, including performing
literature reviews, outlining study methods and findings, and editing manuscripts prior to
submission
• Assist with abstract and presentation submissions for local, regional, national, and
international conferences
• Assist with writing protocols for CARE studies, including Institutional Review Board
applications and informed consent documents, as well as defining project timelines and
maintaining study amendments and continuing reviews
• Collaborate with the principal investigator to develop standard operating procedures and
templates to improve efficiency and consistency across all studies
• Oversee all Institutional Review Board communications regarding projects
• Monitor progression of clinical trials against project milestones
• Oversee all study procedures, compliance, and communication with all collaborating
institutions for multi-site trials
• Oversee all data collection in collaboration with clinical research coordinators for accuracy
and compliance
• Oversee internal and external audits and coordinate all processes with Data Safety and Monitoring Boards for all clinical trials
• Act as the point of contact for CARE members to provide direction and guidance regarding
day-to-day issues and activities as well as interpretation of hospital and regulatory policies
• Maintain centralized training records for all research staff
• Maintain and update CARE email distribution lists and manage the CARE meeting
schedule, including presentations, journal clubs, and guest speakers
• Work with the Development Office to support activities for CARE donors, including Patient
Advisory Councils
• Oversee program website to ensure content is current and accurate; manage CARE study
email accounts and respond to inquiries; submit study team reimbursements
Management responsibilities will include the following:
• Manage hiring process for new clinical research coordinators and project manager positions
• Onboard and oversee new research staff, interns, and volunteers
• Serve as liaison regarding issues related to human resources
• Assess computer equipment acquisition and training needs
• Manage CARE research space
• Oversee system access and support the use of research technology systems
• Perform other managerial and administrative responsibilities as assigned to support the
evolving needs of the CARE research program
Additional Job Details (if applicable)
• Master's degree or PhD preferred
• Minimum of 5 years of research experience preferred
Remote Type
Onsite
Work Location
60 Fenwood Road
Scheduled Weekly Hours
40
Employee Type
Regular
Work Shift
Day (United States of America)
Pay Range
$78,936.00 - $128,928.80/Annual
Grade
8
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:
2200 The Brigham and Women's Hospital, Inc. 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.

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