Research Coordinator Jobs in Massachusetts
Research Coordinator jobs in Massachusetts are among the most active in the country, concentrated in academic medical centers, biotechnology firms, and public health agencies, with openings ranging from entry-level clinical trial assistants to senior protocol managers. Boston, Cambridge, and Worcester anchor the hiring market, where institutions like Massachusetts General Hospital, Dana-Farber Cancer Institute, and Brigham and Women's Hospital maintain ongoing research coordinator pipelines. The most in-demand specialties are oncology clinical trials, epidemiological studies, and biotech drug development research. See the openings below and apply to the ones that match your experience.
Find Research Coordinator JobsOverview
Showing 5 of 79+ Research Coordinator jobs
- Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA
- Identify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up calls
- Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data
- Conduct preliminary quality assurance reviews of study data
- Assist with financial /operational aspects of grant and contracts. May be responsible for clinical research billing review within the required timeframe
- Present study status reports related to assigned research projects
- Contribute to data presentations and Institutional Review Board (IRB) processes
- Track and maintain study related information in the data management system within the required timeframe Provide detailed written summaries from literature searches and related sources to serve as a resource for the study team and clinicians/PIs
- Contribute to the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
- Responsible for monitoring the inventory of research related supplies
- Document and collect data/ samples for research related procedures performed during participant study visits. Ensure clinicians and/or PI accurately document their study activities according to protocol.
- Monitor strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines. Identify and resolve issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance
- Comply with all safety and infection control standards appropriate to this position
- Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices Perform other duties as required.
- Bachelor’s degree in a scientific or health related field, or equivalent experience
- 1-3 years of related experience
- Ability to travel off site locations
- Obtain consent of research participants in accordance with the IRB approved protocols and all applicable regulations including HIPAA
- Identify, schedule and/or conduct participant study visits, tests and/or interviews/telephone follow up calls
- Ensure accuracy and completion of all regulatory documentation, including local or central IRB and study data
- Conduct preliminary quality assurance reviews of study data
- Assist with financial /operational aspects of grant and contracts. May be responsible for clinical research billing review within the required timeframe
- Present study status reports related to assigned research projects
- Contribute to data presentations and Institutional Review Board (IRB) processes
- Track and maintain study related information in the data management system within the required timeframe Provide detailed written summaries from literature searches and related sources to serve as a resource for the study team and clinicians/PIs
- Contribute to the design, development, and documentation of study related data and collection tools, (e.g. questionnaires, treatment data and/or therapeutic checklists)
- Responsible for monitoring the inventory of research related supplies
- Document and collect data/ samples for research related procedures performed during participant study visits. Ensure clinicians and/or PI accurately document their study activities according to protocol.
- Monitor strict adherence to all study protocols, including all regulatory requirements adhering to appropriate federal, local and institutional guidelines. Identify and resolve issues with protocol compliance. Keep principal investigator and manager aware of any issues regarding compliance
- Comply with all safety and infection control standards appropriate to this position
- Adhere to Good Clinical Practice (GCP) guidelines and all human subject protection practices Perform other duties as required.
- Bachelor’s degree in a scientific or health related field, or equivalent experience
- 1-3 years of related experience
- Ability to travel off site locations
See All 79 Research Coordinator Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
Find Research Coordinator JobsResearch Coordinator Jobs by City in Massachusetts
Where Massachusetts roles are concentrated, by current openings.
Research Coordinator Job Market in Massachusetts
A snapshot from current Massachusetts openings, updated as new roles post.
Who's Hiring
- Massachusetts General Hospital15
- Beth Israel Lahey Health13
- Dana-Farber Cancer Institute9
- Boston University4
- Tufts Medical Center4
Top Industries Hiring
- Healthcare & Medical Services
- Biotechnology & Pharmaceuticals
What Massachusetts Employers Look For
The qualifications that appear most often in research coordinator jobs across Massachusetts.
- Bachelor's degree in life sciences, public health, or a related field required
- Experience with IRB submissions, protocol management, and regulatory documentation
- Familiarity with clinical trial management systems such as OnCore, REDCap, or Medidata
- Knowledge of FDA regulations and Good Clinical Practice guidelines
- Strong data collection, participant recruitment, and record-keeping skills
- Ability to coordinate across multidisciplinary teams in fast-paced research environments
Research Coordinator Jobs in Massachusetts: Frequently Asked Questions
How do you become a research coordinator in Massachusetts?
Most research coordinator roles in Massachusetts require a bachelor's degree in a life science, nursing, public health, or a related field. While Massachusetts does not issue a state license specific to research coordination, many employers and academic medical centers strongly prefer or require the Certified Clinical Research Coordinator credential from the Association of Clinical Research Professionals or the Society of Clinical Research Associates certification. Gaining experience through a hospital research department, university lab, or biotech internship is the most direct path into the field.
Which companies hire research coordinators in Massachusetts?
Employers hiring research coordinators in Massachusetts right now include Massachusetts General Hospital, Beth Israel Lahey Health, and Dana-Farber Cancer Institute, based on current listings on Migrate Mate as of August 2026. Massachusetts's deep concentration of academic medical centers, biotechnology companies, and contract research organizations means openings are distributed across hospital systems, life science campuses, and public health agencies throughout the state.
Which Massachusetts cities have the most research coordinator jobs?
Boston, Burlington, and Brookline have the most research coordinator openings in Massachusetts. Boston and Cambridge dominate because they are home to the state's largest academic medical centers, teaching hospitals, and the Kendall Square biotech corridor, while Worcester draws consistent demand from UMass Memorial Medical Center and the University of Massachusetts Medical School research enterprise.
Are there remote research coordinator jobs in Massachusetts?
Yes, but they are limited. Research coordination often requires on-site patient contact, specimen handling, and direct protocol oversight, which makes fully remote work less common than in purely analytical roles. About 26% of research coordinator openings tied to Massachusetts are remote or hybrid as of August 2026, with remote work most accessible for data management, regulatory affairs coordination, and sponsor-facing administrative functions.
How can I get hired as a research coordinator in Massachusetts with little or no experience?
The most realistic entry path is applying to research assistant or clinical trial assistant roles at Massachusetts academic medical centers, which regularly hire candidates without prior research experience and provide structured on-the-job training. Institutions like Massachusetts General Hospital, Boston Medical Center, and Dana-Farber Cancer Institute post entry-level research support positions that build directly toward coordinator responsibilities. A background in patient care, laboratory work, or public health data collection is a competitive advantage, and earning a Good Clinical Practice training certificate before applying helps differentiate candidates who are new to the field.
Where can I find and apply to research coordinator jobs in Massachusetts?
You can find and apply to research coordinator jobs in Massachusetts on Migrate Mate, which lists current openings from employers across the state. Search the listings to find roles that match your experience level and specialty area, then apply directly to the positions that fit.
See All 79 Research Coordinator Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
Find Research Coordinator Jobs