Clinical Research Coordinator Jobs in Massachusetts
Clinical Research Coordinator jobs in Massachusetts are among the most active in the country, concentrated in academic medical centers, pharmaceutical companies, and biotechnology firms at every level from entry-level research assistants through senior coordinators and lead CRCs. Boston, Cambridge, and Worcester anchor the hiring market, with institutions like Massachusetts General Hospital, Dana-Farber Cancer Institute, and Pfizer's Massachusetts operations consistently posting openings. Oncology trials, rare disease research, and Phase I through Phase III drug studies are the most in-demand specializations across the state. Find a role that fits below and apply directly.
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Showing 5 of 61+ Clinical 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 61 Clinical Research Coordinator Jobs in Massachusetts
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Find JobsClinical Research Coordinator Jobs by City in Massachusetts
Where Massachusetts roles are concentrated, by current openings.
Clinical Research Coordinator Job Market in Massachusetts
A snapshot from current Massachusetts openings, updated as new roles post.
Who's Hiring
- Massachusetts General Hospital13
- Beth Israel Lahey Health12
- Dana-Farber Cancer Institute9
- Tufts Medical Center4
- Boston University3
Top Industries Hiring
- Healthcare & Medical Services
- Biotechnology & Pharmaceuticals
What Massachusetts Employers Look For
The qualifications that appear most often in clinical research coordinator jobs across Massachusetts.
- Bachelor's degree in life sciences, nursing, or a related health field required
- ACRP or SOCRA certification (CCRC or CCRP) strongly preferred by Massachusetts employers
- Minimum one to two years of direct clinical trial coordination or research experience
- Working knowledge of FDA regulations, ICH-GCP guidelines, and IRB submission processes
- Proficiency with electronic data capture systems such as REDCap, Medidata Rave, or similar platforms
- Strong communication skills for coordinating with investigators, sponsors, and study participants
Clinical Research Coordinator Jobs in Massachusetts: Frequently Asked Questions
How do you become a clinical research coordinator in Massachusetts?
Most clinical research coordinator roles in Massachusetts require at minimum a bachelor's degree in a life science, nursing, or health-related field. Massachusetts does not issue a state-specific license for the role, but employers across the state strongly favor candidates who hold ACRP's Certified Clinical Research Coordinator (CCRC) credential or SOCRA's Certified Clinical Research Professional (CCRP). Entry-level candidates typically gain experience through hospital research departments, academic medical centers, or contract research organizations before pursuing certification.
How much do clinical research coordinators make in Massachusetts?
Clinical research coordinators in Massachusetts earn a median of about $267,290 a year, based on May 2025 Bureau of Labor Statistics wage data, ranging from around $153,490 for the lowest 10% to over $329,820 for the top 10%. Pay rises with experience, specialty, and employer.
Which companies hire clinical research coordinators in Massachusetts?
Employers hiring clinical 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 teaching hospitals, biotech companies, and contract research organizations means consistent hiring across both clinical and industry settings throughout the year.
Which Massachusetts cities have the most clinical research coordinator jobs?
Boston, Burlington, and Brookline have the most clinical research coordinator openings in Massachusetts. Boston and Cambridge dominate because of the density of academic medical centers, major hospital networks, and the Kendall Square biotechnology corridor, while Worcester draws consistent hiring from UMass Memorial Health and the city's growing life sciences presence.
Are there remote clinical research coordinator jobs in Massachusetts?
Yes, but they're limited. About 24% of clinical research coordinator openings tied to Massachusetts are remote or hybrid as of August 2026, reflecting the hands-on, site-based nature of most trial coordination work. The tasks most amenable to remote work include regulatory document preparation, data entry and query resolution, and sponsor communications, while patient visits and site monitoring almost always require in-person presence.
How can I get hired as a clinical research coordinator in Massachusetts with little or no experience?
The most realistic entry path is securing a research assistant or clinical trials assistant role at one of Massachusetts's large academic medical centers, such as Brigham and Women's Hospital, Boston Children's Hospital, or UMass Memorial Health, which regularly hire candidates with a relevant bachelor's degree and no direct CRC experience. Lateral moves from positions like medical assistant, clinical data associate, or study coordinator support roles are common. Completing a Good Clinical Practice training course and beginning the CCRC or CCRP exam requirements while employed gives newer candidates a measurable edge.
Where can I find and apply to clinical research coordinator jobs in Massachusetts?
You can find and apply to clinical research coordinator jobs in Massachusetts on Migrate Mate, which lists current openings across the state. Find the roles that fit your experience and apply directly.
See All 61 Clinical Research Coordinator Jobs in Massachusetts
Find roles in Massachusetts that match your experience and apply in just a few clicks.
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