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Clinical Risk Manager Jobs in Raleigh, NC (NOW HIRING)

IQVIA

Clinical Trial Lead

Durham, NC · On-site +1

Job Posting Title- Clinical Trial Lead Location: Home-based in the U.S. Responsibilities & Key ... Provide coaching on project planning, risk management, and problem-solving to ensure global ...

IQVIA, Inc.

Clinical Trial Lead

Durham, NC · On-site

Job Posting Title- Clinical Trial Lead Location: Home-based in the U.S. Responsibilities & Key ... risk management, and problem-solving to ensure global alignment and adoption of process and ...

IQVIA

Clinical Trial Lead

Durham, NC · On-site +1

Job Posting Title- Clinical Trial Lead Location: Home-based in the U.S. Responsibilities & Key ... Provide coaching on project planning, risk management, and problem-solving to ensure global ...

Aerogen Ltd

Clinical Trial Manager

Morrisville, NC · On-site

The assigned clinical trial may be of high complexity or high risk. • Ensure clinical trial ... • Manage CRAs assigned to clinical trials and activities related to site qualification ...

IQVIA

Clinical Program Manager

Durham, NC · On-site

$93K - $285K/yr

Anticipating risk and implementing mitigation strategies * Managing study team assignments ... A minimum of 5 years' in Clinical Project Management in industry/CRO/business experience is ...

IQVIA

Clinical Program Manager

Durham, NC

$93K - $285K/yr

Anticipating risk and implementing mitigation strategies * Managing study team assignments ... A minimum of 5 years' in Clinical Project Management in industry/CRO/business experience is ...

IQVIA, Inc.

Clinical Program Manager

Durham, NC · On-site

$93K - $285K/yr

Anticipating risk and implementing mitigation strategies * Managing study team assignments ... A minimum of 5 years' in Clinical Project Management in industry/CRO/business experience is ...

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Clinical Risk Manager information

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 Raleigh, NC?

For Clinical Risk Manager jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Clinical Risk Manager jobs in Raleigh, NC look for?

The top searched job categories for Clinical Risk Manager jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Clinical Risk Manager jobs?

Cities near Raleigh, NC with the most Clinical Risk Manager job openings:

Clinical Risk Manager jobs near you
Infographic showing various Clinical Risk Manager job openings in Raleigh, NC as of August 2026, with employment types broken down into 92% Full Time, 4% Part Time, and 4% Contract. Highlights an 81% In-person, and 19% Remote job distribution.

Senior Global Clinical Study Manager

IQVIA, Inc.

Durham, NC • On-site

Full-time

Re-posted 25 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

62nd of 224 rated it services

Job description

IQVIA Biotech is a full-service CRO purpose-built to serve biotech sponsors. With over 25 years of experience, we offer agile, therapeutically aligned solutions and trusted partnerships that help bring breakthrough treatments to patients faster.
Drive global clinical trials from first site activation to final patient visit-own the strategy, accelerate delivery, and shape the future of clinical research worldwide.
Required Experience
  • ✅ 2+ years of global study management experience
  • ✅ Experience across multiple countries/regions
  • ✅ Phase I-III clinical trials experience (Phase III required)
  • ✅ Oncology experience required
  • ✅ Ability to work across multiple therapeutic areas

Job Overview
We are seeking a Global Study Manager responsible for the end-to-end planning, execution, and delivery of clinical trial site management activities across global studies. This role ensures successful site selection, activation, monitoring oversight, and closeout-while balancing speed, quality, and cost. You will serve as the primary point of contact for clients, lead cross-functional teams, and ensure compliance with ICH-GCP, regulatory requirements, and study protocols. This is a highly visible role that combines strategic leadership, operational execution, and financial oversight.
Key Responsibilities
Global Study & Site Leadership
  • Lead site management strategy from study award through close-out
  • Oversee site identification, selection, activation, and recruitment performance
  • Ensure clinical monitoring processes meet study needs and timelines
  • Partner with CRAs to optimize enrollment, data quality, and compliance

Project & Stakeholder Management
  • Serve as primary client contact and own key customer relationships
  • Lead cross-functional teams across regions and cultures
  • Facilitate internal and external meetings, including executive presentations
  • Drive collaboration across stakeholders, vendors, and functional leads

Operational Excellence & Risk Management
  • Develop and manage integrated study plans and risk mitigation strategies
  • Proactively identify risks and implement corrective/preventative actions
  • Monitor study timelines, enrollment trends, and data quality metrics
  • Ensure compliance with GCP, SOPs, protocols, and regulatory standards

Financial & Contract Management
  • Manage study financials, including forecasting and revenue acceleration
  • Identify and manage out-of-scope work and change orders
  • Oversee Billing Unit Reviews (BURs) and expense approvals
  • Track performance against budget and Estimate at Completion (EAC)

Quality & Compliance
  • Maintain TMF health and ensure timely document submission
  • Develop quality monitoring plans and compliance metrics
  • Ensure adherence to study tools, training materials, and processes

Team Leadership & Development
  • Lead and mentor cross-functional project teams
  • Support CRA and team training on therapeutic areas and study-specific needs
  • Foster collaboration, knowledge sharing, and continuous improvement

Qualifications
Required
  • Bachelor's degree in life sciences or related field
  • 5+ years of clinical research/monitoring experience, including 2 years in a clinical study management role
  • Strong knowledge of ICH-GCP, FDA regulations, and clinical trial processes
  • Experience managing global clinical trials and multi-regional teams
  • Demonstrated experience in project financial management

Core Competencies
  • Exceptional communication and stakeholder management skills
  • Strong problem-solving and risk mitigation capabilities
  • Ability to influence without authority in matrix organizations
  • High attention to detail and quality-driven mindset
  • Proficiency in Microsoft Office and clinical systems (e.g., CTMS, EDC)

Why Join Us
  • Work on cutting-edge global trials across therapeutic areas
  • Collaborate with top talent in a dynamic, global environment
  • Make a direct impact on patient outcomes worldwide

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $93,100.00 - $232,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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