Top 102 Clinical research site manager Jobs in Boston, Ma

Clinical Research Manager
Tufts University —Boston, MA
- $74,000 - $111,000 a year
- Hybrid work
- Nursing
- 5 years
- HIPAA
13d
Clinical Research Manager
RevBio, Inc. —Lowell, MA
- Full-time
- Hybrid work
- 5 years
- Engineering
- Public speaking
- Work from home
Quick Apply
Clinical Research Program/Project Manager
The General Hospital Corporation —Boston, MA
- $63,252.80 - $102,596.00 a year
- Full-time
- Hybrid work
- Spanish
- 5 years
- Writing skills
- Opportunities for advancement
Quick Apply
3d
Clinical Research Manager - Breast Oncology
Dana-Farber Cancer Institute —Boston, MA
- $77,400 - $102,800 a year
- Full-time
- Analysis skills
- Bachelor's degree
- Recruiting
Site Manager
DM CLINICAL RESEARCH GROUP —Brookline, MA
- $100,000 - $120,000 a year
- Writing skills
- Mid-level
- Bachelor's degree
Clinical Research Project Manager - Breast Oncology
Dana-Farber Cancer Institute —Boston, MA
- $76,910 - $85,295 a year
- Full-time
- 3 years
- Bachelor's degree
- Computer skills
Clinical Research Associate II
AbbVie —Boston, MA
- $84,500 - $162,000 a year
- Full-time
- Remote
- Nursing
- Mid-level
- Organizational skills
- Paid holidays
- Health insurance
Clinical Research Associate Manager
The General Hospital Corporation —Boston, MA
- $63,252.80 - $102,596.00 a year
- Full-time
- Vital signs
- 3 years
- Master's degree
- Opportunities for advancement
Quick Apply
2d
Clinical Research Program / Project Manager
The General Hospital Corporation —Boston, MA
- $63,252.80 - $102,596.00 a year
- Full-time
- Hybrid work
- Microsoft Excel
- 3 years
- Bachelor's degree
- Opportunities for advancement
Quick Apply
3d
Project Manager
Alira Health —Boston, MA
- $115,000 - $145,000 a year
- Full-time
- Customer service
- Bachelor of Science
- English
Clinical Study Operations Manager
Beacon Biosignals —Boston, MA
- $90,000 - $110,000 a year
- Remote
- 5 years
- English
- Travel
- Paid time off
Quick Apply
13d
Clinical Research Associate
Alira Health —Boston, MA
- $85,000 - $125,000 a year
- Full-time
- Bachelor of Science
- English
- Mid-level
Clinical Trial Manager
Biogen —Cambridge, MA
- $117,000 - $157,000 a year
- Full-time
- Hybrid work
- 5 years
- Office
- Bachelor's degree
- Paid parental leave
- Employee stock purchase plan
1d
Clinical Research Coordinator – Ophthalmology
Andover Eye Associates Inc —Andover, MA
- From $28 an hour
- Part-time
- Patient monitoring
- HIPAA
- Mid-level
Quick Apply
Region Manager
Care Access —Boston, MA
- $95,000 - $115,000 a year
- Up to 50% travel
- Inventory management
- Pass drug screening
- Health savings account
- Paid holidays
Senior Manager, Clinical Study Quality Lead (Hybrid)
Vertex Pharmaceuticals —Boston, MA
- $137,800 - $206,800 a year
- Full-time
- Hybrid work
- 6 years
- Project management
- Bachelor's degree
- Loan repayment program
- Health insurance
Clinical Research Associate (CRA) – Temporary 6 Month Contract
Lighthouse Lab Services —Waltham, MA
- $45 an hour
- Temporary
- Nursing
- Medicine
- English
- Flexible schedule
Quick Apply
1d
Senior/Clinical Trial Manager (CTM)
Vor Bio —Boston, MA
- $140,000 - $195,000 a year
- 5 years
- Bachelor of Science
- Bachelor's degree
- Health insurance
- 401(k)
Research Project Manager, Infectious Diseases
Boston Medical Center —Boston, MA
- $66,000 - $96,000 a year
- Email
- Mid-level
- 3 years
- Master's degree
- Health insurance
- Dental insurance
Manager, RBQM
Moderna, Inc. —Cambridge, MA
- $109,200 - $174,600 a year
- Full-time
- 6 years
- Data analysis skills
- Office
- Paid time off
- Adoption assistance

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Clinical Research Manager

Tufts University -
Boston, MA

Apply Now

Job Details

$74,000 - $111,000 a year
13 days ago

Qualifications

Document compliance management
Record keeping
Clinical study protocols and reports
HIPAA compliance
Project documentation
Procedural guides
Clinical trial risk management
Operations coordination
HIPAA
Orientation and onboarding programs (healthcare teaching and curriculum development)
Schedule management
Supervising experience
Managing clinical research teams
Mentoring
Developing new training programs
Clinical trial standard operating procedures
Implementing research protocols
Communication with regulatory authorities for clinical trials
Managing projects
Research and development project management
Cross-functional collaboration
Onboarding process management
Ethical review application preparation
Cross-functional team management
Standard operating procedures (SOPs)
Project risk management
Project stakeholder communication
Cross-functional communication
Research compliance audit records management
Research compliance quality assurance records management

Full Job Description

Overview:

The Department of Molecular Biology and Microbiology at Tufts University School of Medicine works to improve global health by using molecular genetics and innovation to address fundamental and medically related problems in microbiology. Training is a core tenet of the department's approach, with students, postdocs, and staff serving as key drivers of its scientific impact. Founded on community building, mentorship, and collaboration, the department is committed to fostering a diverse, inclusive scientific community that welcomes a range of perspectives to produce more innovative and impactful science.

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 clinical and data-collection sites across New England. Reporting to study leadership, this role provides study-wide project management and serves as the primary regulatory lead for the Tufts single IRB, coordinating across clinical operations, data management, laboratory operations, investigative project teams, documentation, training, and stakeholder communications. The ideal candidate brings strong clinical research operations experience, excellent organizational and communication skills, and the ability to manage complex timelines, cross-functional workflows, and competing priorities across multiple institutions.

Serve as the operational center of the study through the Coordinating Center, which owns and drives study-wide infrastructure and execution, including procedures, training, participant materials, progress tracking, and cross-group coordination.
Serve as primary regulatory lead for the Tufts single IRB of record: prepare and maintain submissions, modifications, continuing reviews, reportable new information, consent revisions, reliance agreements, and the study regulatory binder; advise investigators and site staff on compliance strategy across sites.
Maintain study-wide timelines, milestones, and dependencies; manage risks, decisions, and action items using appropriate project-management tools; and oversee implementation of protocol amendments and operational changes across all hubs and sites.
Create, maintain, and update study Manuals of Procedures, SOPs, workflows, and controlled documentation.
Develop and deliver onboarding, refresher, and ongoing training and guidance for study coordinators and site staff across hubs.
Track enrollment and retention across hubs and sites, identify barriers, develop participant-facing retention materials, and work with hub teams on solutions.
Serve as operational liaison to the Diagnostic Core (sample-kit logistics, specimen workflows, enrollment-season readiness, consent preferences) and the Data Center (REDCap updates, data requests, reports, data-quality activities), keeping deliverables on schedule and resolving bottlenecks.
Oversee Tufts hub operations and Tufts-affiliated sites, including site activation, enrollment preparation, and ongoing support; train, onboard, supervise, and support Tufts study coordinators and delegated staff.
Serve as the operational link among the investigative project teams, Data Center, and Diagnostic Core to support sample requests, clinical and diagnostic data needs, analysis support, and selection criteria; prepare enrollment and retention metrics and progress reports for leadership and external stakeholders.

What We're Looking For:

Basic Requirements:
Knowledge and experience typically acquired by:

Advanced degree in clinical research, public health, project management, health administration, life sciences, nursing, or a related field, or equivalent experience.
At least 5 years of progressively responsible clinical research experience, including managing complex, multi-site or multi-institutional studies.
Strong IRB experience, including single-IRB oversight and negotiating or managing reliance agreements.
Demonstrated project-management experience: timeline development, milestone tracking, risk management, dependency tracking, and stakeholder communication.
Experience supervising, training, or leading clinical research staff.
Experience developing and maintaining MOPs, SOPs, training materials, study workflows, onboarding tools, or controlled documentation.
Experience supporting study recruitment, enrollment tracking, participant retention, and follow-up workflows, including developing participant-facing retention materials.
Ability to coordinate work across clinical operations, regulatory, data-management, laboratory, and investigator teams.
Excellent written and verbal communication skills; strong organizational skills and ability to manage multiple priorities in a fast-paced, highly collaborative environment.
Knowledge of Good Clinical Practice, human-subjects protections, HIPAA, and applicable clinical research regulations.
Ability to travel to clinical sites as needed.

Preferred Qualifications:

Experience managing NIH-funded clinical or translational research.
Familiarity with REDCap sufficient to understand data-team workflows and communicate effectively about data collection, reports, and database changes.
Ability to independently access and analyze study data using R, SAS, Python, or similar tools to build enrollment, retention, and operational reports that inform decisions.
Experience coordinating biospecimen collection, laboratory workflows, or biorepository procedures.
Formal project-management training or certification.
Familiarity with infectious-disease, longitudinal studies, or biorepository research

Salary Range: Minimum $74,000.00, Midpoint $92,500.00, Maximum $111,000.00

Apply Now

Refine Your Search

clinical research site manager jobs in boston, ma

Clinical Research Manager

Clinical Research Manager

Clinical Research Program/Project Manager

Clinical Research Manager - Breast Oncology

Site Manager

Clinical Research Project Manager - Breast Oncology

Clinical Research Associate II

Clinical Research Associate Manager

Clinical Research Program / Project Manager

Project Manager

Clinical Study Operations Manager

Clinical Research Associate

Clinical Trial Manager

Clinical Research Coordinator – Ophthalmology

Region Manager

Senior Manager, Clinical Study Quality Lead (Hybrid)

Clinical Research Associate (CRA) – Temporary 6 Month Contract

Senior/Clinical Trial Manager (CTM)

Research Project Manager, Infectious Diseases

Manager, RBQM

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