1

Clinical Risk Manager Jobs in Delaware (NOW HIRING)

Director Claims Management

Wilmington, DE ยท On-site

$121K - $193K/yr

Reporting to the Vice President of Risk Management , you'll lead the claims management function, oversee high-profile litigation, collaborate with physicians, clinical leaders, legal partners, and ...

next page

Showing results 1-20

Clinical Risk Manager information

See Delaware salary details

$75.1K

$100.5K

$132K

How much do clinical risk manager jobs pay per year?

As of Jul 10, 2026, the average yearly pay for clinical risk manager in Delaware is $100,518.00, according to ZipRecruiter salary data. Most workers in this role earn between $84,995.00 and $122,093.00 per year, depending on experience, location, and employer.

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 highest salary for a risk manager?

The highest salary for a clinical risk manager can exceed $120,000 annually, especially for those with extensive experience, advanced certifications, or working in large healthcare organizations. Senior risk managers or those in leadership roles may earn higher compensation, often supplemented with bonuses and benefits.

How to become a clinical risk manager?

To become a clinical risk manager, individuals typically need a bachelor's degree in healthcare, nursing, or a related field, followed by relevant experience in healthcare settings. Many pursue certifications such as the Certified Professional in Healthcare Risk Management (CPHRM) to enhance their qualifications. Strong knowledge of healthcare regulations, risk assessment skills, and the ability to analyze clinical data are essential for this role.

How much does a risk manager get paid?

A clinical risk manager typically earns between $70,000 and $120,000 annually, depending on experience, location, and the size of the healthcare organization. Advanced certifications and expertise in healthcare compliance can lead to higher salaries.

What are the key skills and qualifications needed to thrive as a Clinical Risk Manager, and why are they important?

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.

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.

What does a clinical risk manager do?

A clinical risk manager oversees patient safety and quality of care within healthcare organizations by identifying, assessing, and mitigating clinical risks. They analyze incident reports, develop safety protocols, and ensure compliance with healthcare regulations, often using data analysis tools and requiring relevant certifications such as Certified Professional in Healthcare Quality (CPHQ).
What are popular job titles related to Clinical Risk Manager jobs in Delaware? For Clinical Risk Manager jobs in Delaware, the most frequently searched job titles are:
What cities in Delaware are hiring for Clinical Risk Manager jobs? Cities in Delaware with the most Clinical Risk Manager job openings:
Global Head of R&D & Clinical Development Sourcing

Global Head of R&D & Clinical Development Sourcing

Incyte Corporation

Wilmington, DE โ€ข On-site

Other

This job post hasย expired today.ย Applications are no longer accepted.


Job description

Overview

A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity

Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.

Position Summary
The Senior Director, R&D & Clinical Development Sourcing is a strategic leadership role responsible for developing, executing, and optimizing sourcing strategies across all R&D, Clinical Development, and Scientific Services categories. This leader partners closely with Clinical Operations, R&D Leadership, Development Operations, Biometrics, Regulatory, Quality, and Finance to ensure the organization secures best in class CROs, service providers, technology platforms, and scientific suppliers that enable speed, quality, and innovation in the drug development lifecycle.
This role oversees a team of category leads and sourcing managers supporting the end to end value chain for preclinical research, clinical operations, biometrics, scientific services, and external development partnerships. The Senior Director will be responsible for driving strategic supplier management, ensuring operational excellence, enabling cross functional alignment, and delivering measurable value to the organization through cost optimization, risk mitigation, and enhanced performance.

Key Responsibilities
Strategic Leadership & Business Partnership
* Develop a multi year R&D and Clinical Development sourcing strategy aligned with therapeutic, pipeline, and corporate objectives.
* Serve as lead procurement partner to R&D, Clinical Operations, and Development leadership teams.
* Influence senior stakeholders and build consensus around sourcing strategies, supplier selection, and operational models.
* Represent Procurement in governance forums for study planning, vendor oversight, budget management, and external partnerships.
Category Strategy & Value Delivery
* Lead category strategies across CROs, laboratories, bioanalytical services, scientific services, eCOA/eClinical platforms, biometrics, and functional service provider (FSP) models.
* Drive competitive sourcing events, RFPs, master service agreements, and provide input to study level contracting, when necessary.
* Identify and execute cost avoidance, cost savings, operational efficiencies, and value creation initiatives.
* Ensure sourcing strategies consider quality, compliance, capacity, innovation, and risk.
Supplier Relationship Management (SRM)
* Establish and oversee strategic supplier governance across key CROs, labs, and technology providers.
* Partner with QA, Clinical Operations, and Development leadership to manage performance, risk, audits, KPIs, and escalations.
* Develop long term partnerships that support speed, quality, and scientific excellence.
Team Leadership & Development
* Build, lead, and mentor a high performing procurement team that supports clinical and R&D categories.
* Set clear goals, ensure accountability, and champion professional development.
* Embed a culture of collaboration, continuous improvement, and partnership across the team.
Operational Excellence & Process Improvement
* Strengthen sourcing processes related to vendor selection, study startup timelines, bid defenses, governance, and ongoing operational performance.
* Ensure consistent compliance with procurement policies, legal, quality, and regulatory requirements.
* Collaborate with Finance and FP&A to support budget planning, accruals, and necessary forecasting from vendors.
Risk Management & Compliance
* Assess and mitigate vendor, operational, regulatory, and geopolitical risks associated with external R&D/Clinical suppliers.
* Ensure appropriate due diligence, robust contracting, and governance frameworks.

Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.

Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.

We Respect Your Privacy

Learn more at: http://www.incyte.com/privacy-policy

The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.

You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.

You can learn more about Incyte's data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable).

Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.