Top 13 Research coordinator Jobs in Providence Ri

Clinical Research Coordinator II
Panoramic Health —Providence, RI
- Full-time
- Spanish
- Patient monitoring
- Laboratory experience
Quick Apply
7d
Administrative Research Coord
Care New England Health System —Pawtucket, RI
- Full-time
- Microsoft Excel
- Microsoft Outlook
- Computer literacy
Clinical Research Coordinator II - Attleboro
Dana-Farber Cancer Institute —Attleboro, MA
- $56,000 - $62,700 a year
- Full-time
- Computer literacy
- Mid-level
- Bachelor's degree
Clin Rsrch Project Coord I
Care New England Health System —Pawtucket, RI
- Full-time
- Management
- Computer literacy
- Mid-level
Clinical Trials Research Coordinator
Brown University Health —Providence, RI
- $64,480.00 - $106,412.80 a year
- 8 hour shift
- Nursing
- Vital signs
- Hospital
Clinical Research Coordinator II
Iterative Health —Providence, RI
- Patient monitoring
- HIPAA
- Mid-level
Quick Apply
12d
Clinical Research Coordinator II - Foxborough
Dana-Farber Cancer Institute —Foxborough, MA
- $56,000 - $62,700 a year
- Full-time
- Mid-level
- Databases
- Bachelor's degree
Coordinator, Graduate School of Oceanography/Research - (2 Positions)
University of Rhode Island —Kingston, RI
- $65,000 - $78,000 a year
- Multiple hires
- Word processing
- Office
- University
Senior Clinical Research Coordinator - Milford
Dana-Farber Cancer Institute —Milford, MA
- $73,600 - $83,000 a year
- Full-time
- 3 years
- Bachelor's degree
- Travel
Sr Clinical Research Prgm Coord 2
Brown University Health —Providence, RI
- $64,480.00 - $106,412.80 a year
- 8 hour shift
- Nursing
- Microsoft Excel
- Management
10d
Coordinator, NIUVT (National Institute of Undersea Vehicle Technology)
University of Rhode Island —Kingston, RI
- $70,000 - $75,000 a year
- Online Application
- Word processing
- Mid-level
- Office
Clinical Laboratory Scientist (Ancillary Testing Coordinator)
US Veterans Health Administration —Providence, RI
- $107,583 - $139,861 a year
- Part-time
- Background check
- Pass drug screening
- English
- Loan repayment program

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Administrative Research Coord
Care New England Health System —Pawtucket, RI
Schedules appointments and answers telephone. Skilled in filing, typing, and general computer skills. Bachelor's Degree Required; equivalent combination of…
Clin Rsrch Project Coord I
Care New England Health System —Pawtucket, RI
Basic computer skills, e.g. familiarity with Microsoft software, completing spreadsheet/data entry. Aids in preparation of IRB protocols, amendments, annual…

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Clinical Research Coordinator to coordinate and perform daily clinical research activities in accordance with approved protocols administered by the non-cancer…
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Clinical Research Coordinator I - RI Biobeh Fox
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Recruits, consents and enrolls subjects according to ICH/GCP regulations, and subjects’ rights through institutional IRB, federal and state regulations; answers…
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Clinical Research Coordinator II

Panoramic Health -
Providence, RI

Quick Apply

Job Details

Full-time
7 days ago

Qualifications

Medication dispensing
Data integrity assurance
Vascular access
Data quality checks
Document compliance management
Nephrology
Direct patient care
Spanish
Operational analysis
Patient flow optimization
Informed consent
Patient monitoring
Research ethical considerations
Adverse event reporting
Clinical incident reports
Operations coordination
Filing
Patient weighing scales
Laboratory experience
Care documentation
English
Phlebotomy specimen handling
Mid-level
Patient safety
Research project coordination
Data integrity and documentation
Schedule management
ICH guidelines
Clinical staff training
Policy & process development

Full Job Description

Nephrology Associates, Inc. | Providence, RI
Advance Clinical Research. Improve Kidney Care.

Nephrology Associates, Inc. is seeking an experienced Clinical Research Coordinator II (CRC II) to join our clinical research team in Providence, Rhode Island. This role offers the opportunity to play a key part in the execution of clinical research studies while working closely with investigators, physicians, clinic staff, patients, sponsors, and the broader research team.

The CRC II will take ownership of day-to-day study coordination at the site level, with a strong focus on patient recruitment and enrollment, study execution, regulatory and protocol compliance, data quality, and patient safety. The ideal candidate is organized, proactive, and comfortable managing multiple studies and a high volume of patients while maintaining a high standard of accuracy and quality.

What You'll Do
Study Start-Up & Site Readiness

Read, understand, and operationalize assigned research protocols and study requirements.
Prescreen patients and identify potentially eligible research participants.
Train site staff on study purpose, procedures, and requirements; maintain appropriate training documentation.
Evaluate study resources and coordinate with clinic leadership to ensure the site is prepared for successful study execution.
Develop and implement workflows that improve recruitment, enrollment, patient flow, and study operations.

Patient Recruitment & Enrollment

Proactively identify and recruit potentially eligible patients through collaboration with physicians, clinic staff, and the research team.
Communicate study eligibility criteria and research opportunities to referring physicians and clinic staff.
Partner with the Central Research team, including the Central Enrollment Team, to meet or exceed referral, consent, and enrollment targets.
Obtain and document informed consent in accordance with ICH/GCP, protocol requirements, and site SOPs.
Promote a positive patient experience while prioritizing patient safety and ethical research practices.

Study Coordination & Patient Visits

Coordinate and plan subject visits according to protocol-specific schedules and requirements.
Ensure visits and procedures are completed within protocol-defined windows and minimize protocol deviations.
Perform basic clinical procedures, including vital signs, height, weight, blood collection, and ECGs.
Collect, process, and ship laboratory specimens according to protocol requirements.
Dispense and collect investigational product/medication and maintain accurate accountability records.
Monitor patient participation and maintain accurate patient tracking documentation.

Data & Documentation

Complete case report forms (CRFs), electronic data capture systems, and other study documentation accurately and in a timely manner.
Maintain data integrity in accordance with ALCOA principles: Attributable, Legible, Contemporaneous, Original, and Accurate.
Maintain a thorough understanding of study-specific data collection instruments and ensure data are collected according to protocol.
Report adverse events and serious adverse events to the appropriate IRB, sponsor, and management within required timelines.
Maintain accurate study files, logs, source documentation, and patient records.

Monitoring & Quality Oversight

Prepare for and support sponsor/CRO monitoring visits.
Ensure source documents are organized, complete, and readily available for monitoring.
Respond to monitor follow-up letters in a timely manner and ensure outstanding items are resolved.
Maintain current temperature logs, investigational product accountability records, and other required study documentation.
Resolve data queries and outstanding action items promptly.
Maintain compliance with study protocols, site SOPs, ICH/GCP, IATA, FDA regulations, and applicable research requirements.

Site Operations & Collaboration

Coordinate with location administration to ensure appropriate space, equipment, supplies, and other resources are available for study activities.
Build strong working relationships with physicians, clinic staff, patients, sponsors, CROs, and internal research teams.
Identify operational challenges and proactively implement solutions to improve study performance.
Perform other duties and responsibilities as assigned.

What We're Looking For

3–5 years of clinical research experience, preferably in a coordinator role with increasing responsibility.
Bachelor's degree in a health-related field preferred.
Medical Assistant (MA) certification preferred.
Good Clinical Practice (GCP) and/or IATA certification preferred.
ACRP or SOCRA certification preferred.
Experience in CKD, nephrology, vascular access, or a related therapeutic area is a plus.
Bilingual English/Spanish skills preferred.
Strong knowledge of medical terminology and clinical research practices.
Working knowledge of GCP, IATA, FDA regulations, and research compliance requirements.
Demonstrated ability to manage multiple studies and a high volume of patients while maintaining quality and attention to detail.
Ability to perform basic clinical procedures, including blood draws, vital signs, height, and weight.
Ability to perform ECGs.
Excellent organizational, interpersonal, written, and verbal communication skills.
Highly self-motivated and proactive, with the ability to independently drive recruitment, enrollment, data quality, and study execution.
Strong attention to detail and commitment to patient safety and research quality.
Ability to multitask, prioritize competing responsibilities, and work effectively in a fast-paced clinical environment.

Why Join Us?
This is an opportunity to join a clinical research program focused on advancing care for patients with kidney disease while gaining exposure to the full spectrum of site-level research operations. The CRC II will have meaningful ownership of study execution and the opportunity to make a direct impact on patient recruitment, research quality, and the development of new treatment options for patients with kidney disease.

The Company is committed to the principles of equal employment. We are committed to complying with all federal, state, and local laws providing equal employment opportunities, and all other employment laws and regulations. It is our intent to maintain a work environment which is free of harassment, discrimination, or retaliation because of age, race, color, national origin, ancestry, religion, sex, pregnancy (including childbirth, lactation and related medical conditions), physical or mental disability, genetic information (including testing and characteristics), veteran status, uniformed servicemember status, or any other status protected by federal, state, or local laws. The company is dedicated to the fulfillment of this policy in regard to all aspects of employment, including but not limited to recruiting, hiring, placement, transfer, training, promotion, rates of pay, and other compensation, termination, and all other terms, conditions, and privileges of employment.

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Refine Your Search

research coordinator jobs in providence ri

Clinical Research Coordinator II

Administrative Research Coord

Clinical Research Coordinator II - Attleboro

Clin Rsrch Project Coord I

Clinical Trials Research Coordinator

Clinical Research Coordinator II

Clinical Research Coordinator II - Foxborough

Coordinator, Graduate School of Oceanography/Research - (2 Positions)

Senior Clinical Research Coordinator - Milford

Sr Clinical Research Prgm Coord 2

Coordinator, NIUVT (National Institute of Undersea Vehicle Technology)

Clinical Laboratory Scientist (Ancillary Testing Coordinator)

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