Clinical Research Manager Jobs in Rhode Island
Clinical Research Manager jobs in Rhode Island concentrate in the life sciences and academic medical sectors, with steady demand from entry-level coordinators moving into management through senior directors overseeing multi-site trials. Most openings are in Providence and East Providence, where institutions like Brown University Health, Lifespan, and Care New England anchor the hiring market. Trial management for oncology, cardiovascular research, and rare-disease studies are the most consistently sought specialties. Find a role that fits below and apply directly.
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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 Manager Jobs in Rhode Island
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Find JobsClinical Research Manager Jobs by City in Rhode Island
Where Rhode Island roles are concentrated, by current openings.
Clinical Research Manager 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 manager jobs across Rhode Island.
- Bachelor's or advanced degree in life sciences, nursing, or a related clinical field
- Minimum five years of clinical research experience including at least two in management
- Demonstrated knowledge of ICH-GCP guidelines and FDA regulations for clinical trials
- Experience managing site budgets, regulatory submissions, and IRB correspondence
- Proficiency with electronic data capture systems such as Medidata Rave or Veeva Vault
- Strong communication skills for coordinating investigators, sponsors, and cross-functional teams
Clinical Research Manager Jobs in Rhode Island: Frequently Asked Questions
How do you become a clinical research manager in Rhode Island?
The most direct path is a bachelor's degree in a life science or health-related field, followed by several years working as a clinical research coordinator or associate at a Rhode Island academic medical center or contract research organization. Rhode Island does not require a state-issued license specific to clinical research management, but earning a credential such as the ACRP Certified Clinical Research Professional or SOCRA CCRP designation is widely expected by Providence-area employers and strengthens candidacy significantly.
Which companies hire clinical research managers in Rhode Island?
Companies currently hiring clinical research managers 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 systems and affiliated research institutes tend to post the most consistent openings, particularly for managers with oncology or cardiovascular trial experience.
Which Rhode Island cities have the most clinical research manager jobs?
Providence, Rhode Island, and East Providence have the most clinical research manager openings in Rhode Island. Providence dominates because it is home to the state's largest hospital systems and Brown University's medical and public health programs, while surrounding communities like East Providence and Pawtucket benefit from proximity to those anchor institutions and house satellite research offices and CRO operations.
Are there remote clinical research manager jobs in Rhode Island?
Yes, though opportunities are limited compared to fully desk-based fields, since clinical research managers often need to be on-site to oversee trial operations, conduct site visits, and manage staff directly. About 50% of clinical research manager openings tied to Rhode Island are remote or hybrid as of October 2026, with remote eligibility most common for roles focused on data oversight, sponsor liaison work, or multi-site coordination that does not require daily presence at a single facility.
How can I get hired as a clinical research manager in Rhode Island with little or no experience?
The most realistic entry point is a clinical research coordinator role at one of Providence's major academic medical systems, such as Lifespan or Brown University Health, which regularly bring in candidates from adjacent health positions like medical assistant, research nurse, or pharmacy technician. Building toward a management role typically means completing a GCP certification, taking on regulatory or budget responsibilities within a coordinator role, and expressing interest in a team lead track. Rhode Island's relatively small research community means internal promotion is common for coordinators who demonstrate initiative early.
Where can I find and apply to clinical research manager jobs in Rhode Island?
You can find and apply to clinical research manager jobs in Rhode Island on Migrate Mate, which lists current openings across the state. Find roles that fit your experience and apply directly to the employers posting them.
See All 10 Clinical Research Manager Jobs in Rhode Island
Find roles in Rhode Island that match your experience and apply in just a few clicks.
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