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Clinical Research Program Manager Jobs in Brighton, MA

Tufts University

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 ...

NorthEastern

Research Program Manager

Boston, MA · On-site

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 ...

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Clinical Research Program Manager information

See Brighton, MA salary details

$48.5K

$100.9K

$162.9K

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

As of Aug 28, 2026, the average yearly pay for clinical research program manager in Brighton, MA is $100,922.00, according to ZipRecruiter salary data. Most workers in this role earn between $79,000.00 and $114,400.00 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 job categories do people searching Clinical Research Program Manager jobs in Brighton, MA look for?

The top searched job categories for Clinical Research Program Manager jobs in Brighton, MA are:

What cities near Brighton, MA are hiring for Clinical Research Program Manager jobs?

Cities near Brighton, MA with the most Clinical Research Program Manager job openings:

Clinical Research Program Manager jobs near you

Clinical Research Program Manager

Boston, MA

Shrinerschildrens
See more jobs at Shrinerschildrensexternal

Full-time

Posted 2 days ago

New

Job description

Company Overview

Shriners Children's is an organization that respects, supports, and values each other. Named as the 2025 best mid-sized employer by Forbes, we are engaged in providing excellence in patient care, embracing multi-disciplinary education, and research with global impact. We foster a learning environment that values evidenced based practice, experience, innovation, and critical thinking. Our compassion, integrity, accountability, and resilience define us as leaders in pediatric specialty care for our children and their families.

With 20+ hospitals, outpatient clinics, ambulatory care centers and outreach locations across the globe, we provide excellent care to children up to age 18 regardless of their family's ability to pay or insurance status. Please click here to learn more about our locations.

Job Description

Job Summary
The Clinical Research Program Manager at The Shriners Hospital for Children will oversee and manage all aspects of clinical research programs, ensuring compliance with ethical guidelines, regulatory requirements, and institutional policies. This role involves strategic planning, operational execution, and the overall success of research initiatives aimed at improving pediatric care.
Key Responsibilities

  • Reporting to the Hospital Administrator and Research Programs Office at SHC International Headquarters, the CRPM provides support and leadership in accordance with SHC's policies and procedures, SHC's hospital regulations, the Code of Federal Regulation, and Good Clinical Practice guidelines, when applicable.

  • The CRPM works closely with the Chief of Staff, SHC scientific and medical staff and other research personnel to ethically recruit and consent SHC's vulnerable pediatric subjects and to appropriately collect and safeguard data.

  • Overall, the CRPM is the site's primary liaison among research participants, local study staff, the local investigator(s) and study sponsor(s).

  • This position's main responsibilities are to help ensure proper study conduct, subject safety, and the quality of data and data safeguards.

  • This position will provide management for the day-to-day operations of the clinical research program, ensure competent and standardized staff practices, and coordinate strategies to enhance interdisciplinary communication and collaboration.


Required Qualifications

  • Bachelors or master's in clinical research, science or other healthcare related field preferred. Without a degree, 5 or more years of specific job-related experience in the administration of clinical research is required.

  • Three years' Clinical research experience, e.g. experience with site management, study management, IRB's and federalregulations regarding clinical research compliance

Preferred Qualifications

  • Certified Clinical Research Coordinator

  • Experience in the coordinationof intergroup or multi-site clinical studies

  • Supervisory or management experience

Compensation is determined based on years of relevant experience and departmental equity.

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