Clinical Research Nurse Jobs in Rhode Island
Clinical Research Nurse jobs in Rhode Island are steadily in demand, concentrated in academic medical centers, pharmaceutical trial sites, and specialty care networks, with openings at every level from entry-level research coordinators to senior clinical research nurses managing complex protocols. The most active hiring is in Providence, with additional openings in Pawtucket and East Providence, anchored by employers such as Lifespan Health System, Care New England, and Brown University Health. Oncology trials, cardiovascular research, and neurology studies represent the most consistently posted specialties in the state. Find a role that fits below and apply directly.
Find Clinical Research Nurse JobsOverview
Showing 5 of 8+ Clinical Research Nurse jobs
Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.
We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.
As a Clinical Research Coordinator II (CRC II) at Iterative Health you will play a critical role in the successful execution of clinical trials by independently coordinating daily study activities and ensuring compliance with protocol requirements, regulatory standards, and patient safety guidelines.
This role is responsible for managing complex studies with minimal oversight while partnering closely with patients, investigators, sponsors, CROs, and internal teams to drive high-quality study execution and enrollment success.
Where You'll Drive Impact
- Independently coordinate and manage industry-sponsored clinical trials from study start-up through closeout with minimal supervision
- Manage complex study visit schedules and protocol-related activities while ensuring adherence to study timelines and requirements
- Lead patient recruitment and retention efforts including chart review, patient outreach, informed consent discussions, and enrollment tracking to support study enrollment goals
- Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs
- Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, investigational product accountability, and phlebotomy, as permitted by applicable regulations, training, and organizational policy
- Process laboratory specimens and prepare shipments in accordance with protocol requirements and applicable IATA regulations
- Maintain accurate, complete, and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms
- Ensure high-quality data entry and timely resolution of data queries in accordance with sponsor expectations and established timelines
- Serve as a primary point of contact for study participants throughout study participation
- Maintain ongoing communication with sponsors, CROs, investigators, site leadership, and internal teams to proactively resolve study-related issues
- Prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections
- Review safety reports and ensure appropriate investigator review and documentation in a timely manner
- Maintain inventory and organization of study equipment, supplies, and investigational products onsite
- Contribute to process improvement initiatives to enhance site performance, operational efficiency, and patient experience
- Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies
- Maintain compliance with all site SOPs, privacy standards, and research protocols
- May support onboarding and mentorship of junior research staff and coordinators
- Perform job related duties as requested
What You Bring to the Team
- Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required
- 3-5 years of clinical research or healthcare experience required
- Experience in [gastroenterology, hepatology, cardiology] therapeutic areas preferred
- CCRC® — Certified Clinical Research Coordinator or CCRP® — Certified Clinical Research Professional or equivalent clinical research certification preferred
- Strong organizational skills and attention to detail
- Ability to manage competing priorities in a fast-paced environment
- Ability to read, interpret, and apply research protocols and clinic policies
- Proficiency with CTMS, EDC systems, and standard office software applications
- Familiarity with CTMS or EDC systems preferred
Physical Requirements
- Ability to sit, stand, and move throughout clinical and office environments for extended periods of time
- Ability to lift and move up to 25 pounds as needed
At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.
Iterative Health is a healthcare technology and services company powering the acceleration of clinical research to transform patient outcomes.
We built a leading performance-driven network of 100+ sites across the US, Europe, India, and Australia, conducting research directly in the communities where care is delivered across gastrointestinal, hepatology, obesity, and cardiology. By combining deep clinical trial expertise with cutting-edge AI, we connect sponsors' scientific ambitions with high-performing research teams that expedite and expand access to novel therapeutics for patients in need. Today, Iterative Health is headquartered in Cambridge, Massachusetts, and New York City with 250+ employees world-wide.
As a Clinical Research Coordinator II (CRC II) at Iterative Health you will play a critical role in the successful execution of clinical trials by independently coordinating daily study activities and ensuring compliance with protocol requirements, regulatory standards, and patient safety guidelines.
This role is responsible for managing complex studies with minimal oversight while partnering closely with patients, investigators, sponsors, CROs, and internal teams to drive high-quality study execution and enrollment success.
Where You'll Drive Impact
- Independently coordinate and manage industry-sponsored clinical trials from study start-up through closeout with minimal supervision
- Manage complex study visit schedules and protocol-related activities while ensuring adherence to study timelines and requirements
- Lead patient recruitment and retention efforts including chart review, patient outreach, informed consent discussions, and enrollment tracking to support study enrollment goals
- Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and site SOPs
- Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, investigational product accountability, and phlebotomy, as permitted by applicable regulations, training, and organizational policy
- Process laboratory specimens and prepare shipments in accordance with protocol requirements and applicable IATA regulations
- Maintain accurate, complete, and timely study documentation including source records, informed consent forms, CTMS updates, and case report forms
- Ensure high-quality data entry and timely resolution of data queries in accordance with sponsor expectations and established timelines
- Serve as a primary point of contact for study participants throughout study participation
- Maintain ongoing communication with sponsors, CROs, investigators, site leadership, and internal teams to proactively resolve study-related issues
- Prepare for and support sponsor, CRO, and regulatory monitoring visits, audits, and inspections
- Review safety reports and ensure appropriate investigator review and documentation in a timely manner
- Maintain inventory and organization of study equipment, supplies, and investigational products onsite
- Contribute to process improvement initiatives to enhance site performance, operational efficiency, and patient experience
- Support the protection of human research participants in compliance with federal regulations, GCP, HIPAA, and institutional policies
- Maintain compliance with all site SOPs, privacy standards, and research protocols
- May support onboarding and mentorship of junior research staff and coordinators
- Perform job related duties as requested
What You Bring to the Team
- Associate's or Bachelor's degree in a scientific, healthcare, or related discipline required
- 3-5 years of clinical research or healthcare experience required
- Experience in [gastroenterology, hepatology, cardiology] therapeutic areas preferred
- CCRC® — Certified Clinical Research Coordinator or CCRP® — Certified Clinical Research Professional or equivalent clinical research certification preferred
- Strong organizational skills and attention to detail
- Ability to manage competing priorities in a fast-paced environment
- Ability to read, interpret, and apply research protocols and clinic policies
- Proficiency with CTMS, EDC systems, and standard office software applications
- Familiarity with CTMS or EDC systems preferred
Physical Requirements
- Ability to sit, stand, and move throughout clinical and office environments for extended periods of time
- Ability to lift and move up to 25 pounds as needed
At Iterative Health, we're actively working towards creating an environment that is representative of the diversity of patients our technology serves. We are focused on building an equitable and inclusive culture, and by extension, hiring process. If you require any accommodations to make the application process or interviewing experience more accessible to you, please contact CandidateAccommodations@iterative.health.
See All 8 Clinical Research Nurse Jobs in Rhode Island
Find roles in Rhode Island that match your experience and apply in just a few clicks.
Find Clinical Research Nurse JobsClinical Research Nurse Jobs by City in Rhode Island
Where Rhode Island roles are concentrated, by current openings.
Clinical Research Nurse Job Market in Rhode Island
A snapshot from current Rhode Island openings, updated as new roles post.
Who's Hiring
Top Industries Hiring
- Education
- Healthcare & Medical Services
What Rhode Island Employers Look For
The qualifications that appear most often in clinical research nurse jobs across Rhode Island.
- Active Rhode Island RN license issued or recognized by the Rhode Island Board of Nursing
- At least one year of clinical nursing experience in a relevant specialty area
- Experience with clinical trial protocols, GCP guidelines, and informed consent processes
- Proficiency in electronic data capture systems and clinical trial management platforms
- Strong knowledge of FDA regulations and ICH guidelines governing clinical research
- CCRP or CCRC certification preferred or required for senior research nurse positions
Clinical Research Nurse Jobs in Rhode Island: Frequently Asked Questions
How do you become a clinical research nurse in Rhode Island?
You become a clinical research nurse in Rhode Island by first obtaining an active RN license through the Rhode Island Board of Nursing, which requires passing the NCLEX-RN and meeting the Board's education requirements. Most employers then want at least one year of direct clinical experience before moving into research. From there, earning credentials such as the CCRP through the Association of Clinical Research Professionals strengthens your candidacy significantly.
Which companies hire clinical research nurses in Rhode Island?
Companies currently hiring clinical research nurses in Rhode Island include EmVenio Research, Care New England Health System, and Science 37, per current listings on Migrate Mate as of August 2026. Rhode Island's academic medical systems and affiliated trial networks drive the majority of ongoing openings in the state.
Which Rhode Island cities have the most clinical research nurse jobs?
Providence, Wakefield, and North Kingstown have the most clinical research nurse openings in Rhode Island. Providence leads because it is home to the state's largest academic health systems and research institutions, while surrounding cities like Pawtucket and East Providence benefit from proximity to those anchor employers and their affiliated outpatient and specialty trial sites.
How can I get hired as a clinical research nurse in Rhode Island with little or no experience?
The most realistic entry path is applying to clinical research coordinator or research assistant positions at Rhode Island's major health systems, such as Lifespan or Care New England, which occasionally offer new-graduate pathways into their research departments. Lateral moves from oncology, cardiology, or neurology nursing roles are common since those specialties align with the most active trial areas. Completing a Good Clinical Practice training course and pursuing CCRP eligibility early signals commitment to hiring teams.
Where can I find and apply to clinical research nurse jobs in Rhode Island?
You can find and apply to clinical research nurse jobs in Rhode Island on Migrate Mate, which lists current openings from employers across the state. Search the listings, find roles that match your experience and specialty focus, and apply directly to the ones that fit.
See All 8 Clinical Research Nurse Jobs in Rhode Island
Find roles in Rhode Island that match your experience and apply in just a few clicks.
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