Top 299 Clinical study Jobs in Rhode Island

Senior Clinical Study Manager
Veranex, Inc. —Providence, RI
- $125,600 - $179,630 a year
- Full-time
- 5 years
- Bachelor's degree
- Contracts
Quick Apply
Clinical Research Assistant
Brown University Health —Providence, RI
- $41,537.60 - $68,556.80 a year
- 8 hour shift
- Psychiatry
- Hospital
- Bachelor's degree
7d
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 Assistant PD
Brown University Health —East Providence, RI
- $19.97 - $32.96 an hour
- Day shift
- Hospital
- Computer literacy
- Analysis skills
Clinical Research Assistant I (MFM)
Care New England Health System —Providence, RI
- Weekends as needed
- Nursing
- Hospital
- Master's degree
Physician Assistant - Wakefield, RI
Ortho Rhode Island —Wakefield, RI
- $92,600 - $138,900 a year
- Full-time
- Surgery
- Inpatient
- Mid-level
- Paid time off
Quick Apply
Physician Assistant - Wakefield, RI
Ortho Rhode Island —Wakefield, RI
- $92,600 - $138,900 a year
- Full-time
- Surgery
- Inpatient
- Mid-level
- Paid time off
Quick Apply
Registered Nurse
Rhode Island Public Health Institute —Providence, RI
- $75,000 - $90,000 a year
- Full-time
- Spanish
- Nursing
- Medication administration
- Health insurance
- Dental insurance
Quick Apply
14d
Behavior Analyst (BCBA) - Hybrid
Autism Learning Partners —Providence, RI
- $82,000 - $90,000 a year
- 8 hour shift
- Hybrid work
- Experience working with individuals with developmental disabilities
- Current TB test
- Mid-level
- Continuing education credits
- Disability insurance
Quick Apply
Nurse Practitioner/ Physician Assistant
Pulmonary and Sleep Center of New England —Cumberland, RI
- $110,000 - $200,000 a year
- Part-time
- Certified Nurse Practitioner
- Laboratory experience
- Clinic experience
- Paid holidays
- Health insurance
Quick Apply
21h
Physician Assistant - Wakefield, RI
Ortho Rhode Island —Warwick, RI
- $92,600 - $138,900 a year
- Full-time
- Surgery
- Inpatient
- Mid-level
- Paid time off
Quick Apply
Registered Night Sleep Technician
EPOCH SLEEP CENTERS —Lincoln, RI
- $32 - $45 an hour
- Overnight shift
- CPR Certification
- Patient monitoring
- Bachelor of Science
- Health insurance
- Dental insurance
Quick Apply
Nurse Practitioner
HealthDrive —Providence, RI
- Part-time
- Nursing
- Skilled nursing facility
- Writing skills
- Paid training
- Continuing education credits
5d
Travel Mammography Tech - Providence, RI
Siemens Healthineers —Providence, RI
- $2,800 a week
- Full-time
- BLS Certification
- Mid-level
- Travel
- Paid training
- Paid time off
Quick Apply
7d
Clinical Research Asst II
Care New England Health System —Providence, RI
- $21 - $33 an hour
- Weekends as needed
- Inventory management
- Computer literacy
- Office
7d
Clinical Research Program Coordinator
Brown University Health —Providence, RI
- $55,744.00 - $91,956.80 a year
- 8 hour shift
- Management
- Hospital
- Mid-level
Medical Coordinator
Ortho Rhode Island —Warwick, RI
- $19.65 - $24.55 an hour
- Full-time
- Spanish
- Microsoft Excel
- HIPAA
- Health insurance
- Dental insurance
Quick Apply
Clinical Navigator FCU
Care New England Health System —Providence, RI
- $26.36 - $39.55 an hour
- Full-time
- Addiction Medicine
- Hospital
- Word processing
Phlebotomist Outreach
Brown University Health —Providence, RI
- $18.13 - $29.90 an hour
- Part-time
- Patient monitoring
- Hospital
- Outpatient experience
Community Health Worker
Brown University Health —Providence, RI
- $19.97 - $32.96 an hour
- 8 hour shift
- Spanish
- Hospital
- Computer literacy
13d

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clinical study jobs near rhode island

Senior Clinical Study Manager

Veranex, Inc. -
Providence, RI

Quick Apply

Job Details

Full-time
$125,600 - $179,630 a year

Qualifications

Document compliance management
ISO standards
Bachelor's degree
Biomedical regulatory compliance
Clinical quality assurance standards
FDA regulations
Research compliance quality assurance records management

Full Job Description

Veranex’s mission as an Innovation CRO is to improve patient outcomes by accelerating our clients’ innovations to market. As the world’s only end-to-end professional services firm focused on MedTech, we take clients’ Vision to Velocity through our comprehensive service portfolio, with expertise in human centered design and product development, preclinical and clinical research, regulatory affairs, and market access and reimbursement consulting.

About This Role:
The Senior Clinical Study Manager is responsible for planning, executing, and overseeing clinical trials to ensure they are conducted efficiently, ethically, and in compliance with regulatory standards. This role involves collaborating with various stakeholders, including sponsors and regulatory authorities, to drive the successful completion of clinical studies. By managing the operational aspects of the trial, a Clinical Study Manager ensures that high-quality data is generated, contributing to the advancement of medical science and the development of new therapies.

Location: Remote, US

What You Will Do:
Study Management

Lead day-to-day management of study activities and deliverables.
Serve as a liaison with stakeholders across all functional areas of the study.
Manage study budget and timelines.
Manage vendors, including the implementation and coordination of vendor scope of work (SOW).
Serve as a point of contact for issue escalation.
Interact directly with institutions and investigators, execute clinical research initiatives, and ensure alignment with strategic goals.

Study Start-Up, Site Management & Execution

Coordinate and support execution of study projects, including:
Site identification and initiation
Ethics and regulatory approvals
Contracting
Site budgeting and invoicing
Site staff training
Site initiations, routine monitoring, and close-out activities
Identify and establish the suitability of study investigators and sites and liaise with them to ensure compliance with all study requirements, approvals, and agreements.
Lead the development and implementation of key study documents, including study-specific plans, monitoring plans, study reference manuals, and source document templates.
Lead the execution of clinical studies, evaluation and analysis of clinical data, and preparation/review of clinical study reports.

Quality, Compliance & Oversight

Oversee maintenance of clinical and regulatory files, ensuring accurate and timely tracking and documentation.
Oversee the development of clinical reports supporting regulatory submissions.
Oversee monitoring of study conduct and progress, including proactive identification and resolution of issues impacting quality, timelines, budget, or compliance.
Identify and mitigate quality risks and/or issues associated with assigned studies and activities.
Ensure study conduct complies with ethical and regulatory standards, SOPs, GCP, and local regulations.

Performance Tracking & Reporting

Lead the collection, tracking, and reporting of key performance indicators (KPIs), including:
query resolution
safety data collection/issues
product/device reconciliation and shipment
site and patient enrollment
protocol deviations

Strategic & Business Support

Contribute to business development activities as a subject matter expert (SME).
Generate strategy and proposal documentation as directed.

Qualifications

Required:

Bachelor's degree in health sciences or related discipline
Minimum of 5 years of relevant experience in medical device clinical study planning, preferably within a MedTech-oriented CRO
Experience maintaining documentation in compliance with FDA and ISO standards
Ability to independently manage multiple priorities in a fast-paced environment
Strong organizational, analytical, and problem-solving skills
Excellent written and verbal communication skill

Veranex is an equal opportunity employer and prohibits discrimination of any kind. All qualified applicants will receive consideration for employment without regard for race, color, religion or belief, sex (including pregnancy, gender identity or gender expression), sexual orientation, parental or marital status, disability, age, status as a protected veteran, national, social, or ethnic origin, or any other applicable legally protected characteristics.

Quick Apply

Refine Your Search

clinical study jobs in rhode island

Senior Clinical Study Manager

Clinical Research Assistant

Clinical Trials Research Coordinator

Clinical Research Assistant PD

Clinical Research Assistant I (MFM)

Physician Assistant - Wakefield, RI

Physician Assistant - Wakefield, RI

Registered Nurse

Behavior Analyst (BCBA) - Hybrid

Nurse Practitioner/ Physician Assistant

Physician Assistant - Wakefield, RI

Registered Night Sleep Technician

Nurse Practitioner

Travel Mammography Tech - Providence, RI

Clinical Research Asst II

Clinical Research Program Coordinator

Medical Coordinator

Clinical Navigator FCU

Phlebotomist Outreach

Community Health Worker

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