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Global Risk Manager Jobs in Delaware (NOW HIRING)

AirJoule

Global Sourcing Manager

Newark, DE · On-site

Cost & Risk Management * Lead RFQ development and competitive bid processes across a global ... supplier base, including should-cost analysis and contract negotiation. * Maintain the Costed Bill ...

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Global Risk Manager information

See Delaware salary details

$51.5K

$111.7K

$170.1K

How much do global risk manager jobs pay per year?

As of Aug 6, 2026, the average yearly pay for global risk manager in Delaware is $111,652.00, according to ZipRecruiter salary data. Most workers in this role earn between $90,100.00 and $129,100.00 per year, depending on experience, location, and employer.

What is the difference between Global Risk Manager vs Risk Analyst?

AspectGlobal Risk ManagerRisk Analyst
CredentialsTypically requires advanced degrees (e.g., MBA, risk management certifications)Often requires a bachelor's degree, some certifications preferred
Work EnvironmentStrategic, overseeing risk across multiple regions or departmentsAnalytical, focused on data assessment and reporting
Employer & Industry UsageUsed in multinational corporations, finance, insuranceCommon in finance, banking, and consulting firms

The Global Risk Manager focuses on strategic risk oversight across global operations, requiring advanced credentials and a broad perspective. In contrast, the Risk Analyst concentrates on data analysis and risk assessment at a more operational level. Both roles are essential in risk management but differ in scope and responsibilities.

How does a global risk manager collaborate with other departments to ensure comprehensive risk mitigation across international operations?

A Global Risk Manager works closely with various departments such as compliance, legal, finance, operations, and IT to identify, assess, and mitigate risks that could impact the organization's global activities. This collaboration often involves regular cross-functional meetings, sharing of risk assessments, and developing unified risk management strategies. Effective communication and relationship-building skills are essential, as the role requires aligning diverse teams with differing regional regulations and business practices. By fostering a collaborative environment, Global Risk Managers help ensure that all potential risks are addressed proactively, keeping the company compliant and resilient across borders.

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

To thrive as a Global Risk Manager, you need strong analytical skills, deep knowledge of risk assessment methodologies, and a relevant degree in finance, business, or risk management. Expertise in risk management software (like RSA Archer or SAP GRC), familiarity with international regulations, and certifications such as FRM or CRM are often required. Exceptional communication, critical thinking, and cross-cultural collaboration abilities set top candidates apart in this role. These skills ensure effective identification, mitigation, and communication of global risks, protecting organizational assets and reputation.
What are popular job titles related to Global Risk Manager jobs in Delaware? For Global Risk Manager jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Global Risk Manager jobs in Delaware look for? The top searched job categories for Global Risk Manager jobs in Delaware are:
What cities in Delaware are hiring for Global Risk Manager jobs? Cities in Delaware with the most Global Risk Manager job openings:
Global Risk Manager jobs near you
Infographic showing various Global Risk Manager job openings in Delaware as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $111,652 per year, or $53.7 per hour.

Manager, Global Risk Management & Safety Surveillance Scientist

Incyte Corporation

Wilmington, DE • On-site

Full-time

Re-posted 2 days ago

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.
The job is based in Wilmington Delaware, US. (Minimum 3 days per week in the office. Local candidates or those willing to relocate only).
Job Summary (Primary function)
This Global Risk Management & Safety Surveillance (GRMSS) Scientist collaborates with the GRMSS Physician to characterize the evolving clinical and post-marketing safety profiles for Incyte investigational drugs and/or products, based on analysis of aggregate data sets from internal or external sources and the medical literature. This entails drafting, reviewing, and refining portions of periodic aggregate safety reports (including DSURs, RMPs, and PBRERs), IB/RSI updates, safety-related product label updates, and responses to health authority requests for information. The GRMSS Scientist performs the signal detection activities and review process for clinical and post-marketing data, including signal detection, evaluation, and verification; potential sources of data for signal detection include Incyte, external marketing partners, or contracted business entities. The Scientist in this position documents signal detection activities and communicates appropriate summaries to internal stakeholders and external partners.
Qualifications
Education
  • Healthcare degree (e.g., BSN, CRNP, Pharm.D.) preferred (or relevant scientific degree buttressed by industry experience).
  • Oncology Nurse Practitioners, Physician Assistants, and Pharmacists seeking to transition into the pharmaceutical industry are encouraged to apply.
  • Willingness to travel (less than 5%) to domestic conferences, as applicable, with reasonable accommodations made for individuals with disabilities.

Experience
  • 0-2 years of relevant experience.
  • Experience may be gained through clinical practice, fellowship, residency, research, internships, or industry roles.
  • Recent graduates, fellows, residents, and early-career professionals are encouraged to apply.
  • Prior pharmaceutical, biotechnology, pharmacovigilance, or drug safety experience is beneficial but not required.

Knowledge & Skills
  • Strong written and verbal communication skills.
  • Interest in drug safety, risk management, pharmacovigilance, and drug development.
  • Strong attention to detail and ability to work collaboratively across functions.
  • Willingness to learn global pharmacovigilance regulations, safety surveillance activities, and risk management processes.

Essential Functions of the Job (Key responsibilities)
  • Provide overall support to the GRMSS Physicians for global risk management and safety surveillance activities.
  • Support/contribute to the discussions on risk management safety strategies to internal stakeholders (e.g., Clinical Development, Medical Affairs, Regulatory Affairs, Quality Assurance, Commercial, Translational & Experimental Medicine, and Legal).
  • Contribute to preparedness for regulatory authority inspection and internal audits of Incyte Pharmacovigilance by following standard operation procedures and processes.
  • Participate in internal safety process improvements and updates.
  • Support the GRMSS Physician in evaluating safety data to compile reference safety information for Incyte products, included in the Investigator Brochures, Core Data Sheets, and regional labels.
  • Participate in the review of integrated summaries of safety, clinical overviews, and other registration documents (e.g., for new and supplemental NDAs and/or ex-US new drug submissions for late-phase drug development candidates and marketed products) in collaboration with the GRMSS team, including professionals from Clinical Development, Medical Writing, Statistics, and Regulatory Affairs.
  • In collaboration with the GRMSS Physician/Scientist, support the preparation of Aggregate Reports (DSURs, PSURS, PADERS, etc.) for Incyte clinical trial programs and marketed products.
  • Provide support as needed to the GRMSS Physician in reviewing periodic literature for new and important information regarding Incyte products.
  • Support the GRMSS Physician/Scientist in the preparation of initial Risk Management Plans (RMPs) and subsequent updates throughout the lifecycle of a medicinal product.
  • Perform drug signal management activities, including the drafting of signal evaluation reports for Incyte's portfolio of investigational and marketed products.
  • Collaborate with GRMSS Physician in the development of clinical trial and post-marketing risk management safety strategies.
  • Support GRMSS Medical Professional and coordinate/lead Safety Management Team meetings.

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.
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