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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Showing 5 of 8+ Clinical Research Manager 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 Manager Jobs in Rhode Island
Find roles in Rhode Island that match your experience and apply in just a few clicks.
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
- Healthcare & Medical Services
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 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 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, Wakefield, and North Kingstown 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.
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 8 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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