Associate Director, Supply Chain Logistics & Compliance

The Company:With deep expertise in chemistry, Nuvalent is working to create selective medicines designed with the goal to address the needs of patients with cancer. Nuvalent is an exciting early-stage company, bringing together experienced scientists and industry veterans with a proven track record in drug discovery, oncology drug development, and company building. The Role:Reporting to the Director of Supply Chain Management, the Associate Director, Supply Chain Logistics & Compliance will lead import / export, trade compliance and support global logistics who thrives in a dynamic, fast-paced, team-oriented, and collaborative environment. This role is responsible for ensuring compliance, efficiency, and cost-effective cross-border movements of goods, while supporting global supply chain strategies, regulatory requirements, and commercial objectives. The ideal candidate brings subject matter expertise in import/export processes, customs compliance and global distribution networks, along with proven leadership expertise.This position will allow for growth within the company and contribute to your valuable experience in establishing policies and procedures for the Supply Chain department during a critical time. You will work closely with many cross-functional areas and will be able to contribute to their practices for a more efficient, cost-effective, and compliant supply chain. Our fast-paced environments and hands-on opportunities will challenge you to innovate and learn while having fun with supportive and passionate colleagues.Responsibilities:Lead Import/Export activities, ensuring full compliance with global customs regulations, export controls and trade sanctionsOversee product classification (HTC) valuation, country of origin, and accurate preparation of shipping documentationDevelop, implement, and continuously improve global trade compliance processes, SOPS, and internal control mechanismsDirect liaison with customs authorities, brokers and regulatory agenciesMonitor and interpret evolving global trade regulations, ensuring timely implementation of changesDesign and manage global distribution networks to support commercial and clinical supply needsDrive optimization of routes, carriers and distribution models to balance cost, speed, and complianceEstablish and track KPIs such as customs clearance time, on-time delivery, cost per shipment, and compliance metricsEnsure visibility across the supply chain through tracking and proactive exception managementIdentify and mitigate risks related to cross-border shipments including delays, regulatory issues, and geopolitical factorsEnsures adherence to cGMP and GSP/GDP regulations.Partner with Quality and Regulatory to support inspections and ensure audit readinessDemonstrated leadership experience in global distribution and cross-border operationsAdvanced knowledge of international trade regulations, customs compliance, and export control frameworkStrong understanding of Incoterms, tariff classification, customs valuation, and documentationUnderstands comprehensive global pharmaceutical regulatory requirements (e.g. cGMP, GDP, 21 CFR Part 11, and Annex 6, 13) and knowledgeable of relevant commercial laws and regulatory guidelines.Competencies:Effective communicator with strong stakeholder managementDetail-oriented with a strong compliance mindsetEncourages collaboration, innovation and new ideas while integrating information from various sources. Demonstrated ability to develop and foster relationships with internal and external stakeholders. Flexibility with changing priorities, ability to think critically, strong attention to detail, and ability to work well under pressure.Excellent problem solving, communication and organization skills.Qualifications: Education Required: Bachelor’s degree in business administration, Operations Management, Engineering or similar required. Advanced degree preferred.10+ years progressive experience in logistics within the biotech/pharmaceutical industry with strong emphasis on import/export and trade compliance.Due to the global nature of the company, early morning or evening meetings are required. Potential Travel: 10%Experience in change management, deviation investigation and CAPA implementation.Experience in vendor oversight and managing external partnerships and relations.Experience with small molecule supply chain.Experience with lane risk assessments, and shipping lane/process qualification including IQ, OQ, PQAdditional Information:Nuvalent is committed to fair and equitable compensation practices, aiming to provide employees with competitive total rewards packages.The targeted salary range reflects what Nuvalent reasonably and in good faith expects to offer for this position at the time of posting, but the final salary determination may be within or outside this range based on various factors, including, but not limited to, experience, skills, education, and market factors. The range will be reviewed regularly