Top 391 Clinical research associate Jobs in Brighton, Ma

Research Coordinator
VA Boston Healthcare System —Boston, MA
- Full-time
- Background check
- Mid-level
- Administrative experience
- Health savings account
- Health insurance
Quick Apply
9d
Clinical Researcher — Night Shift
Orbit Technologies, Inc. —Charlestown, MA
- $30 - $50 an hour
- 8 hour shift
- In-person
- Entry level
- Relocation assistance
Quick Apply
Clinical Research Associate (CRA) – Temporary 6 Month Contract
Lighthouse Lab Services —Waltham, MA
- $45 an hour
- Temporary
- Nursing
- Medicine
- English
- Flexible schedule
Quick Apply
3d
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
Alira Health —Boston, MA
- $85,000 - $125,000 a year
- Full-time
- Bachelor of Science
- English
- Mid-level
Clinical Research Associate
CTTX Health —Cambridge, MA
- $103,000 - $105,000 a year
- Contract
- Hybrid work
- Nursing
- Mid-level
- 3 years
- Benefits from day one
Quick Apply
Clinical Research Associate - Contract
Lumicell —Waltham, MA
- Contract
- Remote
- Nursing
- Mid-level
- Bachelor's degree
Quick Apply
Clinical Research Associate
Alliance for Clinical Trial in Oncology Foundation —Boston, MA
- $57,000 - $75,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Bachelor of Science
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Clinical Trial Associate
Candel Therapeutics —Needham, MA
- $88,000 - $100,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Mid-level
- Bachelor's degree
Clinical Research Associate II/III - US
Optimapharm d.o.o. —Boston, MA
- $75,000 - $100,000 a year
- Full-time
- Remote
- Nursing
- Computer literacy
- Mid-level
- Health insurance
- Dental insurance
Clinical Assessment Data Operations Associate
Oruka Therapeutics —Waltham, MA
- $104,000 - $125,000 a year
- Remote
- Microsoft Excel
- Computer Science
- Mid-level
1d
Research Associate
Eight Sleep —Boston, MA
- $70,000 - $100,000 a year
- Weekends as needed
- Computer Science
- HIPAA
- Mid-level
Clinical Research Associate
RevBio, Inc. —Lowell, MA
- Full-time
- Hybrid work
- Engineering
- Mid-level
- Travel
- Work from home
Quick Apply
Research Associate
Bruker —Boston, MA
- $62,500 - $100,000 a year
- Full-time
- Bachelor of Science
- Microsoft Office
- Bachelor's degree
- Employee stock purchase plan
- Disability insurance
8d
Clinical Trial Associate
Deciphera Pharmaceuticals —Waltham, MA
- $90,000 - $124,000 a year
- Full-time
- Hybrid work
- Mid-level
- Master's degree
- Bachelor's degree
- Health insurance
- Dental insurance
Quick Apply
Senior Clinical Research Associate - US
Optimapharm d.o.o. —Boston, MA
- $100,000 - $130,000 a year
- Full-time
- Remote
- Nursing
- 5 years
- Computer literacy
- Health insurance
- Dental insurance
Clinical Data Analyst II
Deephealth —Somerville, MA
- $94,000 - $128,000 a year
- Full-time
- Remote
- Bachelor of Science
- HIPAA
- 3 years
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)
Medpace, Inc. —Boston, MA
- Full-time
- Remote
- Mid-level
- Office
- Driver's License
- Health insurance
- Paid time off
22h
Clinical Research Associate
The General Hospital Corporation —Boston, MA
- $20.16 - $29.01 an hour
- Full-time
- Bachelor's degree
- Communication skills
- Entry level
- Opportunities for advancement
Quick Apply
Clinical Research Assistant, Clinical Neurology
Boston University —Boston, MA
- University
- Bachelor's degree
- Neurology
4d

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Research Coordinator

VA Boston Healthcare System
Boston, MA

Quick Apply

Job Details

Full-time
9 days ago

Benefits

Health savings account
Health insurance
Dental insurance
Flexible spending account
Paid time off
Employee assistance program
Vision insurance
Life insurance
Retirement plan

Qualifications

Project reporting
Data privacy laws
EHR systems
Project documentation
Data quality assurance
Administrative experience
Research project coordination
Data integrity and documentation
Research report preparation
Clinical data report preparation
Data collection
Project stakeholder communication
Research compliance quality assurance records management

Full Job Description

Research Coordinator (Health Science Specialist)

VA Boston Healthcare System

Boston, MA 02130

On-site (Full-time, in-person)

This position is based within VA Boston Healthcare System, a leading healthcare system in New England that serves as a major referral center and a hub for clinical research. The organization’s Boston-based bioinformatics center is seeking a Research Coordinator to support regulatory document preparation and submissions for a portfolio of research projects aimed at improving cancer care. The position offers the opportunity to participate in data-driven projects that inform clinical decision-making and enhance outcomes for diverse patient populations.

Under the supervision of Principal Investigators and senior administrative staff, the Research Coordinator will serve as the point of contact for regulatory documentation and submission for a portfolio of oncology research projects. This work supports a learning healthcare system in which insights from existing data directly guide the development, testing, and refinement of clinical decision support and care delivery strategies for older Veterans with cancer.

You will join a multidisciplinary team of clinicians, statisticians, and data scientists at a nationally recognized, Age‑Friendly academic VA health system affiliated with Harvard Medical School and Boston University School of Medicine. This role offers a unique opportunity to contribute to high‑impact research that translates real‑world evidence into improved, patient‑centered cancer care for older patients.

PRIMARY DUTIES:

Perform all aspects of regulatory-related work, including preparation and submission of the following:
new projects to the appropriate committees (e.g., local Research & Development Committee, Central IRB, Office of Research Reviews)
annual status report submissions, continuing reviews, protocol amendments, financial disclosure submissions, and timely reporting of protocol deviations and/or unanticipated events
study closure submissions
Accurately complete regulatory documentation and meet all submission deadlines
Assist with preparation of budgets, statements of work, data use agreements, contracts, deliverables and timelines, data access provisioning
Collaborate with the Principal Investigator (PI) and study team members
Establish and follow processes for regulatory documentation and submissions
Follow center standard operating procedures
Effectively communicate among PI, study team members, sponsor, auditors, and review committee members; keep the PI informed of progress and potential problems
Prepare and maintain study files, documents, and data for internal and external audits
Act as a primary contact and resource for the regulatory submissions for each study

MINIMUM QUALIFICATION:

MUST be a US Citizen and MUST clear a US government background check
BASIC EDUCATION REQUIREMENT: Applicants must possess a bachelor's or graduate/higher level degree with major study in an academic field related to the medical field, health sciences, or allied sciences appropriate to the work of the position. This degree must be from an educational program from an accrediting body recognized by the U.S. Department of Education at the time the degree was obtained.
EXPERIENCE: In addition to meeting the above requirement, applicants must have at least one (1) full year of specialized experience that equipped them with the knowledge, skills, and abilities to successfully perform the duties of this position with specialized experience that includes: coordinating or supporting multiple research or healthcare projects; facilitating communication among multidisciplinary teams and stakeholders; preparing project reports, presentations, and other written communications; supporting research data collection, tracking, and quality assurance activities; working with electronic medical record data, clinical databases, or other healthcare datasets; and assisting with research administrative and regulatory activities in accordance with applicable institutional policies and data privacy requirements.

SUBSTITUTION OF EDUCATION FOR EXPERIENCE: Successful completion of one (1) full year of progressively higher-level graduate education with a major in a field appropriate to the work of this position to substitute for the one year of experience is fully qualifying for this position.

COMBINING EDUCATION AND EXPERIENCE: Combination of successful completed of a graduate education and experience may be used to meet total qualification requirements.

NOTE: Reference OPM website for more information on Qualification Standards: https://www.opm.gov/policy-data-oversight/classification-qualifications/general-schedule-qualification-standards/#url=Occupational-Series

PREFERRED QUALIFICATIONS:

Understanding of regulatory submission processes for research activities within healthcare systems
Experience preparing and submitting research study submissions to regulatory bodies (e.g., IRB, R&D, etc.) in a clinical research or bioinformatics/data science setting
Experience preparing for and undergoing internal and external audits of clinical research documentation
Excellent written and verbal communication, attention to detail, and organizational skills are a must.

POINT OF CONTACT FOR POSITION:

Applicants should submit a cover letter, resume/CV, (must indicate full-time or part-time for each position listed under work experience and # of hours), and unofficial transcripts by Friday, August 28, 2026, with “Research Coordinator” in the e-mail subject line to: [email protected]

Please confirm US citizenship in your cover letter.

EEO/Equal Opportunity Employer

Benefits:

Dental insurance
Employee assistance program
Flexible spending account
Health insurance
Health savings account
Life insurance
Paid time off
Retirement plan
Vision insurance

Work Location: In person

Quick Apply

Refine Your Search

clinical research associate jobs in brighton, ma

Research Coordinator

Clinical Researcher — Night Shift

Clinical Research Associate (CRA) – Temporary 6 Month Contract

Clinical Research Associate II

Clinical Research Associate

Clinical Research Associate

Clinical Research Associate - Contract

Clinical Research Associate

Clinical Trial Associate

Clinical Research Associate II/III - US

Clinical Assessment Data Operations Associate

Research Associate

Clinical Research Associate

Research Associate

Clinical Trial Associate

Senior Clinical Research Associate - US

Clinical Data Analyst II

Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)

Clinical Research Associate

Clinical Research Assistant, Clinical Neurology

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