Clinical Research Jobs in Rhode Island
Clinical research jobs in Rhode Island are concentrated in Providence and the surrounding corridor, where anchor institutions like Brown University Health, Lifespan, and Care New England drive consistent demand for coordinators, associates, and project managers. The most in-demand specialties are oncology trials, cardiovascular studies, and phase II through IV multi-site protocols. Openings range from entry-level coordinator roles to senior CRA and regulatory affairs positions, reflecting the depth of Rhode Island's academic medical infrastructure. See the openings below and apply to the ones that match your experience.
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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 Jobs in Rhode Island
Find roles in Rhode Island that match your experience and apply in just a few clicks.
Find Clinical Research JobsClinical Research Jobs by City in Rhode Island
Where Rhode Island roles are concentrated, by current openings.
Clinical Research 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 jobs across Rhode Island.
- ACRP or SOCRA certification (CCRC, CCRP) strongly preferred or required for most roles
- Bachelor's degree in life sciences, nursing, or a related health field required
- Proficiency with electronic data capture systems such as Medidata Rave or REDCap
- Working knowledge of FDA regulations, ICH-GCP guidelines, and IRB submission processes
- Experience monitoring or coordinating Phase I through IV clinical trials at a sponsor or site
- Strong attention to protocol compliance, source document verification, and adverse event reporting
Clinical Research Jobs in Rhode Island: Frequently Asked Questions
How do you become a clinical research professional in Rhode Island?
Rhode Island does not have a state-issued license specific to clinical research, so the standard path is a bachelor's degree in a life science, nursing, or health-related field followed by an entry-level coordinator role at a hospital, academic medical center, or CRO. Earning ACRP or SOCRA certification demonstrates competency and is frequently required for advancement. Providence-area institutions affiliated with Brown University's medical programs are common starting points for new professionals in the state.
Which companies hire clinical research professionals in Rhode Island?
Rhode Island clinical research roles are posted by Brown University Health, Care New England Health System, and Science 37 and others right now, based on current listings on Migrate Mate as of October 2026. Rhode Island's academic medical systems and the CROs that partner with them account for a large share of active postings across the state.
Which Rhode Island cities have the most clinical research jobs?
Providence, Rhode Island, and East Providence are the cities with the most clinical research openings in Rhode Island. Providence dominates because of its concentration of academic medical centers and Brown University-affiliated research programs, while nearby communities reflect the geographic spread of satellite trial sites and outpatient research facilities tied to the same large health systems.
Are there remote clinical research jobs in Rhode Island?
Yes, but they are limited. About 50% of clinical research openings tied to Rhode Island are remote or hybrid as of October 2026, which reflects the on-site nature of most trial coordination and monitoring work. The roles most likely to offer remote flexibility are data management, medical writing, regulatory affairs, and sponsor-side clinical monitoring positions that do not require direct patient or site contact.
How can I get hired as a clinical research professional in Rhode Island with little or no experience?
The most realistic entry path is applying for a clinical research coordinator I or research assistant role at one of Providence's large health systems, such as those under the Lifespan or Care New England umbrella, which regularly onboard candidates from adjacent roles like phlebotomy, medical assisting, or clinical data entry. A bachelor's degree in a health science and completion of a Good Clinical Practice training course are the credentials that give new applicants an edge before their first coordinator position.
Where can I find and apply to clinical research jobs in Rhode Island?
You can find and apply to clinical research jobs in Rhode Island on Migrate Mate, which lists current openings from employers hiring in the state right now. Search the listings to find roles that match your experience level and specialization, then apply directly to the ones that fit.
See All 10 Clinical Research Jobs in Rhode Island
Find roles in Rhode Island that match your experience and apply in just a few clicks.
Find Clinical Research Jobs