Clinical Research Associate Jobs in Rhode Island
Clinical Research Associate jobs in Rhode Island concentrate in academic medical research, biopharmaceutical development, and hospital-based clinical trials, with openings ranging from entry-level coordinators to senior monitors and project leads. Most hiring is centered in Providence, with additional activity in the Pawtucket and East Providence corridors, where institutions like Brown University Health, Lifespan, and Care New England maintain active research programs. Oncology trials, cardiovascular studies, and rare disease protocols are the most consistently sought specialties in the state. Scan the live roles below and apply to whichever ones fit.
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- Job ID: JR-115304
- Entity: Rhode Island Hospital
- Location Name: Rhode Island Hospital
- City, State: Providence, RI
- Work Type: FULL TIME
- Hours Per Week: 40
- Shift: Day
- Posted Date: 10/22/2026
SUMMARY
Under general supervision, but following established policies and procedures, performs scientific investigative research in areas related to patient care. Researches literature in the field, participates in the design of experimental protocols and develops new procedures to carry out established research objectives. Interviews patients to gather information, prepares and maintains study record, enters data via computer, performs statistical analyses of resultant data. Participates in the qualitative/quantitative analyses of data. May assist in writing presentations and papers for publication based on the research performed. May perform EKG’s and take vital signs during research-based monitoring tests. May also perform blood spinning and shipment of blood and tissue samples as required by protocol. Brown University Health employees are expected to successfully role model the organization's values of Compassion, Accountability, Respect, and Excellence as these values guide our everyday actions with patients, customers and one another.
In addition to our values, all employees are expected to demonstrate the core Success Factors which tell us how we work together and how we get things done. The core Success Factors include:
- Instill Trust and Value Differences
- Patient and Community Focus and Collaborate
RESPONSIBILITIES
Identifies patients meeting criteria for inclusion in clinical research studies, ensuring research protocol eligibility requirements are met. In collaboration with the research investigator, participates in the design of experimental protocols to achieve the scientific objectives of the research project. Develops research methodologies within the parameters of experimental protocols and research objectives to allow quantitative and qualitative evaluation and interpretation of data obtained. Establishes and maintains study record for each participant. Interviews patient and/or family to explain the nature of the study, eliciting cooperation and gathering information to complete study questionnaire. Facilitates obtaining informed consent. May assist to schedule patient appointments and make calls to patients to complete documentation. Reviews medical records to abstract information necessary to complete forms. Requests and follows up on missing data such as laboratory test results and the like. Regularly monitors adherence to protocol; alerts physician when laboratory tests ordered have not been performed, medication protocol not followed, etc. Collects and organizes patient data into appropriate format to facilitate data entry. Creates, modifies as appropriate and maintains study database to meet needs for project. Gathers, tabulates, graphs develops explanatory charts, and analyzes data using statistical methodology. Performs computer-assisted statistical analysis such as multiple antecedent variables, linear regression, frequencies, cross-tabulation and the like. Writes non-complex programs using computer and software-compatible language to reformat information, create new files, etc. Prepares and maintains related graphs and charts or results of data gathered. Participates in quantitative/qualitative analyses of resultant information. May provide functional guidance to subordinate research staff assigned to the project to provide clarification of protocol, resolve issues, ensure adherence to research protocol procedures and assist in developing their professional skills in reviewing and interpreting statistical trends and the like. Participates in the interpretation of the results of experiences through conferences with principal investigator and other research professionals involved in the study to review data compared to hypothesis and research methodology in instances of inexplicable data. May make recommendation for modification of research protocol based upon initial findings. May assist in writing presentations and papers for publications based on research performed. Regularly reviews relevant literature to research being conducted in order to better understand the project. Maintains and enhances professional expertise through educational opportunities and participation in related teams and conferences. May perform research-based EKG’s, vital signs, blood spinning and shipping of blood and tissue products, in accordance with protocol specifications.
MINIMUM QUALIFICATIONS
BASIC KNOWLEDGE: Bachelor’s Degree in Applied or Life Sciences or related area, including courses in research methodologies and microcomputer systems.
EXPERIENCE: Two to three years progressively more responsible and related experience in the research field. Experience should demonstrate effective working knowledge of statistics, computer programming and research methodology and an in-depth knowledge of the scientific field in which the research is being conducted.
SUPERVISORY RESPONSIBILITY: Provides functional guidance to subordinate research staff assigned to the project. Completion in a laboratory environment with possible exposure to human and animal serum chemical reagents, animal subjects and radioactive materials.
PAY RANGE
$48,068.80 - $79,372.80
LOCATION
Rhode Island Hospital - 593 Eddy Street Providence, Rhode Island 02903
WORK TYPE
M - F, 8:30am - 5:00pm
WORK SHIFT
Day
DAILY HOURS
8 hours
DRIVING REQUIRED
No
Brown University Health is committed to providing equal employment opportunities and maintaining a work environment free from all forms of unlawful discrimination and harassment.
- Job ID: JR-115304
- Entity: Rhode Island Hospital
- Location Name: Rhode Island Hospital
- City, State: Providence, RI
- Work Type: FULL TIME
- Hours Per Week: 40
- Shift: Day
- Posted Date: 10/22/2026
SUMMARY
Under general supervision, but following established policies and procedures, performs scientific investigative research in areas related to patient care. Researches literature in the field, participates in the design of experimental protocols and develops new procedures to carry out established research objectives. Interviews patients to gather information, prepares and maintains study record, enters data via computer, performs statistical analyses of resultant data. Participates in the qualitative/quantitative analyses of data. May assist in writing presentations and papers for publication based on the research performed. May perform EKG’s and take vital signs during research-based monitoring tests. May also perform blood spinning and shipment of blood and tissue samples as required by protocol. Brown University Health employees are expected to successfully role model the organization's values of Compassion, Accountability, Respect, and Excellence as these values guide our everyday actions with patients, customers and one another.
In addition to our values, all employees are expected to demonstrate the core Success Factors which tell us how we work together and how we get things done. The core Success Factors include:
- Instill Trust and Value Differences
- Patient and Community Focus and Collaborate
RESPONSIBILITIES
Identifies patients meeting criteria for inclusion in clinical research studies, ensuring research protocol eligibility requirements are met. In collaboration with the research investigator, participates in the design of experimental protocols to achieve the scientific objectives of the research project. Develops research methodologies within the parameters of experimental protocols and research objectives to allow quantitative and qualitative evaluation and interpretation of data obtained. Establishes and maintains study record for each participant. Interviews patient and/or family to explain the nature of the study, eliciting cooperation and gathering information to complete study questionnaire. Facilitates obtaining informed consent. May assist to schedule patient appointments and make calls to patients to complete documentation. Reviews medical records to abstract information necessary to complete forms. Requests and follows up on missing data such as laboratory test results and the like. Regularly monitors adherence to protocol; alerts physician when laboratory tests ordered have not been performed, medication protocol not followed, etc. Collects and organizes patient data into appropriate format to facilitate data entry. Creates, modifies as appropriate and maintains study database to meet needs for project. Gathers, tabulates, graphs develops explanatory charts, and analyzes data using statistical methodology. Performs computer-assisted statistical analysis such as multiple antecedent variables, linear regression, frequencies, cross-tabulation and the like. Writes non-complex programs using computer and software-compatible language to reformat information, create new files, etc. Prepares and maintains related graphs and charts or results of data gathered. Participates in quantitative/qualitative analyses of resultant information. May provide functional guidance to subordinate research staff assigned to the project to provide clarification of protocol, resolve issues, ensure adherence to research protocol procedures and assist in developing their professional skills in reviewing and interpreting statistical trends and the like. Participates in the interpretation of the results of experiences through conferences with principal investigator and other research professionals involved in the study to review data compared to hypothesis and research methodology in instances of inexplicable data. May make recommendation for modification of research protocol based upon initial findings. May assist in writing presentations and papers for publications based on research performed. Regularly reviews relevant literature to research being conducted in order to better understand the project. Maintains and enhances professional expertise through educational opportunities and participation in related teams and conferences. May perform research-based EKG’s, vital signs, blood spinning and shipping of blood and tissue products, in accordance with protocol specifications.
MINIMUM QUALIFICATIONS
BASIC KNOWLEDGE: Bachelor’s Degree in Applied or Life Sciences or related area, including courses in research methodologies and microcomputer systems.
EXPERIENCE: Two to three years progressively more responsible and related experience in the research field. Experience should demonstrate effective working knowledge of statistics, computer programming and research methodology and an in-depth knowledge of the scientific field in which the research is being conducted.
SUPERVISORY RESPONSIBILITY: Provides functional guidance to subordinate research staff assigned to the project. Completion in a laboratory environment with possible exposure to human and animal serum chemical reagents, animal subjects and radioactive materials.
PAY RANGE
$48,068.80 - $79,372.80
LOCATION
Rhode Island Hospital - 593 Eddy Street Providence, Rhode Island 02903
WORK TYPE
M - F, 8:30am - 5:00pm
WORK SHIFT
Day
DAILY HOURS
8 hours
DRIVING REQUIRED
No
Brown University Health is committed to providing equal employment opportunities and maintaining a work environment free from all forms of unlawful discrimination and harassment.
See All 10 Clinical Research Associate Jobs in Rhode Island
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Find JobsClinical Research Associate Jobs by City in Rhode Island
Where Rhode Island roles are concentrated, by current openings.
Clinical Research Associate Job Market in Rhode Island
A snapshot from current Rhode Island openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Education
What Rhode Island Employers Look For
The qualifications that appear most often in clinical research associate jobs across Rhode Island.
- Bachelor's degree in life sciences, nursing, or a related clinical field required
- Prior experience in clinical trial monitoring or coordination at a CRO or sponsor
- Knowledge of ICH-GCP guidelines and FDA regulatory requirements for clinical research
- Familiarity with electronic data capture systems such as Medidata Rave or Oracle
- Strong site management skills including site qualification, initiation, and monitoring visits
- ACRP or SOCRA certification preferred by most Rhode Island research employers
Clinical Research Associate Jobs in Rhode Island: Frequently Asked Questions
How do you become a clinical research associate in Rhode Island?
Start with a bachelor's degree in a life science, nursing, or health-related field, then gain hands-on experience through clinical trial coordination, data management, or a research assistant role. Rhode Island has no state-issued license specific to clinical research associates, but employers at institutions like Brown University Health and Lifespan strongly favor candidates with ACRP's CCRA credential or SOCRA's CCRP certification. Building a foundation in GCP compliance and site monitoring puts candidates in the strongest position.
Which companies hire clinical research associates in Rhode Island?
Companies currently hiring clinical research associates in Rhode Island include Brown University Health, Care New England Health System, and Science 37, per current listings on Migrate Mate as of October 2026. Rhode Island's academic medical centers and regional CRO offices drive much of the consistent demand for site monitors and research coordinators in the state.
Which Rhode Island cities have the most clinical research associate jobs?
Providence, Rhode Island, and East Providence have the most clinical research associate openings in Rhode Island. Providence anchors the market because Brown University, its affiliated hospitals, and several CRO regional offices are concentrated there, while Pawtucket and East Providence draw additional postings from the research and biomedical operations based along the Seekonk River corridor.
Are there remote clinical research associate jobs in Rhode Island?
Yes, and more than many clinical roles, since experienced monitors often conduct central and remote monitoring in addition to on-site visits. About 50% of clinical research associate openings tied to Rhode Island are remote or hybrid as of October 2026, reflecting the growing acceptance of risk-based monitoring models. Central monitoring, data review, and sponsor oversight work tend to be the most remote-eligible parts of the role.
How can I get hired as a clinical research associate in Rhode Island with little or no experience?
The most realistic entry path is a clinical research coordinator role, which Rhode Island hospitals like those in the Lifespan and Care New England systems use as the primary pipeline for future monitors. Research assistant positions in Brown University's clinical departments also provide documented GCP exposure. Earning a CCRP or CCRA certification while in a coordinator role signals readiness to move into monitoring and separates candidates in a competitive applicant pool.
Where can I find and apply to clinical research associate jobs in Rhode Island?
You can find and apply to clinical research associate jobs in Rhode Island on Migrate Mate, which lists current Rhode Island openings in one place. Search for roles that match your experience level and therapeutic area focus, then apply directly to the ones that fit your background.
See All 10 Clinical Research Associate Jobs in Rhode Island
Find roles in Rhode Island that match your experience and apply in just a few clicks.
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