Top 5 Clinical study manager 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
Research Nurse Manager
Brown University Health —Providence, RI
- $97,718.40 - $195,436.80 a year
- 8 hour shift
- Nursing
- Patient monitoring
- RN License
8d
Sr Research Administrator Clinical Trials
Brown University Health —Providence, RI
- $71,136.00 - $117,353.60 a year
- 8 hour shift
- Microsoft Word
- Microsoft Excel
- Hospital
6d
Research Program Administrator
Brown University Health —Providence, RI
- $67,724.80 - $111,716.80 a year
- 8 hour shift
- 6 years
- Hospital
- Master's degree

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Senior Clinical Study Manager
Veranex, Inc. —Providence, RI
Lead the execution of clinical studies, evaluation and analysis of clinical data, and preparation/review of clinical study reports.
$125,600 - $179,630 a year
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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.

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clinical study manager jobs in rhode island

Senior Clinical Study Manager

Research Nurse Manager

Sr Research Administrator Clinical Trials

Research Program Administrator

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