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Clinical Risk Manager Jobs in Irving, TX (NOW HIRING)

10351

Senior Counsel, Medical Risk Management

Dallas, TX

$138K - $187K/yr

Regularly interacts and collaborates with clinical staff and management to identify, quantify, and mitigate risk liability; strategic thinker who helps clinical staff navigate through legal ...

IQVIA

Senior Global Clinical Study Manager

Dallas, TX · On-site

Drive global clinical trials from first site activation to final patient visit-own the strategy ... Develop and manage integrated study plans and risk mitigation strategies * Proactively identify ...

IQVIA

Senior Global Clinical Study Manager

Dallas, TX · On-site

Drive global clinical trials from first site activation to final patient visit-own the strategy ... Develop and manage integrated study plans and risk mitigation strategies * Proactively identify ...

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Showing results 21-40

All JobsClinical Risk JobsClinical Risk Manager JobsClinical Risk Manager Jobs in Irving, TX

Clinical Risk Manager information

See Irving, TX salary details

$77.3K

$103.4K

$135.7K

How much do clinical risk manager jobs pay per year?

As of Aug 19, 2026, the average yearly pay for clinical risk manager in Irving, TX is $103,353.00, according to ZipRecruiter salary data. Most workers in this role earn between $87,392.00 and $125,536.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a clinical risk manager?

To thrive as a Clinical Risk Manager, you need a solid background in healthcare, risk management, and regulatory compliance, typically supported by a clinical degree and certifications such as CPHRM (Certified Professional in Healthcare Risk Management). Familiarity with incident reporting systems, electronic health records, and risk analysis tools is essential. Strong analytical thinking, communication, and problem-solving skills enable effective collaboration with healthcare teams and leadership. These competencies are vital for identifying, mitigating, and preventing risks to ensure patient safety and regulatory compliance in healthcare organizations.

How does a clinical risk manager collaborate with clinical staff to improve patient safety?

Clinical Risk Managers work closely with nurses, physicians, and other healthcare professionals to identify potential risks and prevent adverse events. They often conduct root cause analyses after incidents, facilitate safety training sessions, and lead multidisciplinary meetings to discuss risk mitigation strategies. By fostering open communication and encouraging reporting of near-misses, they help create a culture of safety and continuous improvement within the healthcare facility.

What is the difference between Clinical Risk Manager vs Clinical Risk Coordinator?

AspectClinical Risk ManagerClinical Risk Coordinator
CertificationsCPHRM, RACCPHRM, RAC (sometimes)
Work EnvironmentHospitals, healthcare organizations, risk management departmentsClinics, healthcare facilities, risk management teams
ResponsibilitiesOversees risk management programs, develops policies, analyzes risksAssists in risk assessments, supports risk mitigation efforts, data collection

The Clinical Risk Manager typically holds more advanced certifications and has broader responsibilities in developing and overseeing risk management strategies. The Clinical Risk Coordinator supports these efforts through data collection and risk assessment assistance. Both roles are essential in healthcare risk management but differ in scope and seniority.

Is healthcare risk management a good career?

Healthcare risk management is a growing field that involves identifying and reducing risks to improve patient safety and compliance. Clinical risk managers typically need strong analytical skills, knowledge of healthcare regulations, and certifications such as Certified Professional in Healthcare Risk Management (CPHRM). It offers opportunities for advancement and a stable career in the healthcare industry.

What do clinical risk managers do?

Clinical risk managers identify, assess, and develop strategies to reduce risks related to patient safety and healthcare quality. They analyze incident reports, implement safety protocols, and ensure compliance with healthcare regulations, often using data analysis tools. Their role helps prevent errors and improve overall clinical outcomes.

What are popular job titles related to Clinical Risk Manager jobs in Irving, TX?

For Clinical Risk Manager jobs in Irving, TX, the most frequently searched job titles are:

What job categories do people searching Clinical Risk Manager jobs in Irving, TX look for?

The top searched job categories for Clinical Risk Manager jobs in Irving, TX are:

What cities near Irving, TX are hiring for Clinical Risk Manager jobs?

Cities near Irving, TX with the most Clinical Risk Manager job openings:

Clinical Risk Manager jobs near you
Infographic showing various Clinical Risk Manager job openings in Irving, TX as of July 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $103,353 per year, or $49.7 per hour.

Senior Regulatory Affairs Specialist

Semler Scientific, Inc.

Dallas, TX • On-site

Full-time

Re-posted 4 days ago

Job description

Description

The Senior Regulatory Affairs Specialist is a key individual contributor supporting regulatory strategy and compliance across the product lifecycle.  


Regulatory and Quality report to the Compliance Department. This position reports to the Chief Compliance Officer. 


Principal Duties & Responsibilities

Participate in internal compliance audits (e.g. FDA, ISO, etc.) and actively participate and represent the company in 3rd party inspections.

Maintain up-to-date knowledge, identify, and monitor applicable standards and guidance documents for relevance, and communicate changes for timely implementation.

Manage, update, and enhance QMS activities and documents to meet compliance needs.

Support the product development team in the evaluation and translation of various complex FDA regulations and ISO standards including, ISO 13485, ISO 14971, IEC 60601-1, IEC 62304, and IEC 62366 into project objectives, deliverables, and activities.

Review regulatory labeling and documents for accuracy and adherence to regulatory requirements, noting deficiencies and inconsistencies.

Provide regulatory analysis and recommendations to support product classification decision and submission pathways.

Assist with preparation of regulatory filings such as 510(k) and DeNovo submissions and subsequent revisions/supplements and amendments by managing associated deliverables and timelines.

Ensure clinical studies adhere to applicable regulations and guidelines, including FDA and ICH standards.

Assist with developing and implementing pre-clinical test strategy and provide guidance to team members on execution strategy.

Support the preparation and submission of clinical trial site ethics review board applications and maintain communication throughout the study.

Develop, review, and update clinical design control documents including providing advice and guidance to product development team on development of technical summaries, clinical risk assessments, product training, instructions for use, design of validation protocols and reports, usability protocols and reports, design and application of FMEAs (Failure Modes and Effects Analysis), for technical and clinical documentation in product development.

Ensure procedural, medical, scientific, and economic factors are considered during cross-functional product development project team meetings.

Design, review and/or conduct literature searches and complete literature reviews for design concept, product development, protocol preparation, clinical risk assessments and/or clinical evaluation reports.

Requirements

Qualifications (Education, Experience, Skills)

BS in health profession or science preferred

10+ years of Regulatory/Clinical experience and relevant accomplishments

ISO 13485:2016 Lead Auditor Certification preferred 

Direct experience within an FDA regulated Class II software medical device organization 

Familiarity and comfort with software terminology and test strategy 

Understanding of economic endpoints to support Current Procedural Terminology (CPT) codes process and Health Technology Assessment (HTA) assessment for market access preferred. 

Demonstrated understanding of advanced technical principles related to regulated environments and harmonized standards

Impeccable attention to detail and organization skills

Strong planning and analytical skills with demonstrated business impact in previous roles

Self-driven with proven ability to simultaneously manage complex projects and timelines while handling the pressure of demanding deadlines

Understands the need for balancing high quality output with a high efficiency level

Excellent written and oral communication skills; technical writing capabilities and ability to convey complex issues in a straightforward manner are a must


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