Pay Range: $82,000.00-$131,200.00 Company Overview:
The people of Memorial Sloan Kettering Cancer Center (MSK) are united by a singular mission: ending cancer for life. Our specialized care teams provide personalized, compassionate, expert care to patients of all ages. Informed by basic research done at our Sloan Kettering Institute, scientists across MSK collaborate to conduct innovative translational and clinical research that is driving a revolution in our understanding of cancer as a disease and improving the ability to prevent, diagnose, and treat it. MSK is dedicated to training the next generation of scientists and clinicians, who go on to pursue our mission at MSK and around the globe.
Important note: MSK is upgrading our application system to enhance your experience. From August 1 through August 11, our job postings will be temporarily unavailable. We encourage you to apply before July 31 or check back on August 12 when our new system goes live. Thank you!
Job Description:
Exciting Opportunity at MSK: Reporting to the Manager, Contracts OPRA in the Grants and Contracts (G&C) unit of the Office of Research and Project Administration (ORPA), the Export Control Analyst plays a critical role in supporting MSK’s Export Control Compliance Program (ECP). This position ensures institutional compliance with U.S. export control regulations and manages collaborative research agreements linked to sponsored research funding.

KEY QUALIFICATIONS:

• Strong knowledge of U.S. export control regulations including EAR, ITAR, and OFAC.
• Experience drafting and negotiating research-related agreements.
• Familiarity with federal contracting regulations (FAR, DFAR, CFR).
• Ability to assess and mitigate institutional risk in research collaborations.

CORE SKILLS:

• Export compliance review and license management.
• Contract negotiation and interpretation.
• Risk assessment and mitigation.
• Stakeholder communication and training development.
• Policy and process improvement.

ROLE OVERVIEW:

• Conduct export control reviews and lead export license applications.
• Develop and maintain Technology Control Plans (TCPs) and compliance documentation.
• Draft, negotiate, and execute collaborative research agreements (funded and non-funded).
• Interpret and apply federal and sponsor-specific contract terms and regulations.
• Collaborate with internal stakeholders (e.g., Legal, Tech Development, Clinical Research) to ensure consistent and compliant agreements.
• Provide training and outreach on export control and contract compliance.
• Lead or contribute to special projects, process improvements, and institutional initiatives.
• Prepare reports and metrics related to export compliance and contract activity.