
Multinational biopharmaceutical company.
Global Trade Compliance Manager - Sanctions Screening and Clinical Valuation Lead at Amgen
About the role
Career Category
Compliance
Job Description
JOIN AMGEN’S MISSION OF SERVING PATIENTS
At Amgen, if you feel like you are a part of something bigger, it’s because you are. Our shared mission—to serve patients living with serious illnesses—drives all that we do. Since 1980, we’ve helped pioneer the world of biotech in our fight against the world’s toughest diseases. With our focus on four therapeutic areas – Oncology, Inflammation, General Medicine, and Rare Disease – we reach millions of patients each year. As a member of the Amgen team, you’ll help make a lasting impact on the lives of patients as we research, manufacture, and deliver innovative medicines to help people live longer, fuller happier lives. Our award-winning culture is collaborative, innovative, and science based. If you have a passion for challenges and the opportunities that lay within them, you’ll thrive as part of the Amgen team. Join us and transform the lives of patients while transforming your career.
Global Trade Compliance Manager
- Sanctions Screening and Clinical Valuation Lead
Live
What you will do:
Sanctions and Ownership Screening:
In this role, you will serve as the global screening lead responsible for executing and continuously improving Amgen’s sanctions and ownership compliance framework under:
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U.S. Department of Treasury – Office of Foreign Assets Control (OFAC)
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U.S. Department of Commerce – Bureau of Industry & Security (BIS)
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Other global regulatory agencies
You will act as the primary escalation point for sanctions screening alerts involving counterparties, transactions, and ownership structures. This includes responsibility for analyzing complex corporate ownership chains to determine applicability of OFAC’s 50% aggregation rule and BIS Entity List/ MEU (Military End User) ownership requirements.
Partnering cross-functionally with Compliance, Legal, Sourcing, Finance, Operations, and Business Units, you will help ensure Amgen’s global activities are conducted in full compliance with international trade laws while mitigating regulatory, financial, and reputational risk.
This role combines investigative rigor, regulatory experience, data analysis, and process innovation.
Key Responsibilities
Sanctions & 50% Ownership Screening Oversight
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Serve as subject matter expert on OFAC 50% Ownership aggregation principles and BIS 50% Entity List alignment requirements
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Conduct enhanced due diligence on counterparties to determine ultimate beneficial ownership (UBO)
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Aggregate ownership interests across direct and indirect shareholders to assess sanctions exposure
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Screen vendors, customers, banks, and other counterparties against:
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OFAC SDN List
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BIS Entity List / Military End User Lists
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Other applicable restricted party lists
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Review, analyze, and adjudicate screening alerts; determine true matches vs. false positives. Serves as primary escalation contact for high-risk sanctions determinations
Investigations & Complex Ownership Analysis
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Identify hidden or indirect sanctioned ownership exposure
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Gather and interpret information from public records, corporate registries, databases, and commercial screening tools
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Develop comprehensive case files documenting findings, risk assessments, and recommended actions
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Prepare clear, well-supported investigative reports for leadership and Legal review
Regulatory Guidance & Risk Mitigation
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Monitor evolving OFAC/BIS and other regulatory developments and enforcement trends
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Provide real-time guidance to internal stakeholders on risk
Technology & Process Optimization
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Leverage screening systems, compliance management tools, and data analytics platforms to improve efficiency
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Identify automation opportunities, including AI-enabled first-pass review capabilities
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Drive process improvements to reduce manual inefficiencies while maintaining compliance integrity
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Partner with systems teams to enhance screening workflows and reporting capabilities
What you will do: Clinical Customs Valuation Lead Key Responsibilities
Responsible for supporting global customs clinical valuation assignments by ensuring accurate customs valuation in compliance with international trade regulations.
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Apply knowledge of trade compliance requirements to support global clinical valuation activities
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Support the assignment of customs values for clinical materials in accordance with World Customs Organization (WCO) valuation principles
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Review dashboards for new product setup and demand forecasts to anticipate valuation needs and prioritize activities
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Support year-end true-up activities for global clinical customs valuation and ensure new values in SAP are entered accurately and timely
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Partner with internal stakeholders to ensure customs values for new clinical materials are accurately entered in SAP
Win
What we expect of you
We seek a professional who combines regulatory expertise, analytical rigor, and sound judgment with the ability to operate in a dynamic global environment.
Basic Qualifications:
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Bachelor’s degree and 4 years of experience in compliance or screening operations, risk management, regulatory affairs, audit, law, or a related field
OR
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Associate’s degree and 8 years of experience in compliance, risk management, regulatory affairs, audit, law, or a related field
OR
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High school diploma / GED and 10 years of experience in compliance, risk management, regulatory affairs, audit, law, or a related field
Preferred Qualifications:
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Basic understanding of WCO customs valuation principles and international trade compliance
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Strong knowledge of:
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OFAC sanctions regulations and 50% aggregation rule
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BIS Entity List / MEU requirements
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Experience conducting ownership due diligence and UBO investigations
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Familiarity with sanctions screening platforms (e.g., Dow Jones, Descartes, MK Denial, Sayari, Kharon, SAP GTS, Oracle GTM)
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Advanced analytical skills and ability to interpret complex ownership structures
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Experience preparing investigative reports for senior leadership
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Proficiency in compliance systems, analytics tools, and AI-enabled monitoring solutions
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Strong project management capabilities
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Excellent written and verbal communication skills
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Demonstrated ability to work independently while collaborating across a global matrix
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High ethical standards and professional integrity
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Adaptable and eager to learn new technologies and regulatory trends impacting regional compliance
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High ethical standards, integrity, and sensitivity to diverse groups, with the ability to influence and resolve conflict constructively
.
Required skills
Trade compliance
Sanctions screening
Regulatory compliance
Risk assessment
Process improvement
Stakeholder management
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About Amgen

Amgen
PublicA biotechnology company that develops and manufactures human therapeutics for various illnesses and diseases.
10,001+
Employees
Thousand Oaks
Headquarters
$138B
Valuation
Reviews
24 reviews
3.6
24 reviews
Work-life balance
3.2
Compensation
3.5
Culture
3.1
Career
2.8
Management
3.4
65%
Recommend to a friend
Pros
Excellent benefits and health benefits
Good pay and compensation
Supportive management and leadership
Cons
Limited career growth and promotion opportunities
Work-life balance challenges and long hours
Bureaucratic processes
Salary Ranges
1,002 data points
Senior/L5
Senior/L5 · Clinical Research Medical Director
1 reports
$374,000
total per year
Base
$288,425
Stock
-
Bonus
-
$374,000
$374,000
Interview experience
5 interviews
Difficulty
3.0
/ 5
Duration
14-28 weeks
Offer rate
40%
Experience
Positive 20%
Neutral 80%
Negative 0%
Interview process
1
Application Review
2
Recruiter Screen
3
Hiring Manager Interview
4
Technical/Case Interview
5
Final Round/Panel Interview
6
Offer
Common questions
Technical Knowledge
Behavioral/STAR
Past Experience
Case Study
Culture Fit
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