Jobs at Lantheus

Architect and govern hybrid infrastructure across on-prem, colocation, and multi-cloud environments. Lead M365, identity (Okta), endpoint (Intune/SCCM/Tanium), DR (Rubrik) and AI-driven automation initiatives. Partner with security and vendors, drive cost optimization, and translate business needs into resilient infrastructure roadmaps.

The Associate Director will partner with commercial teams to generate market insights and support the commercialization of cardiac products, utilizing market research and competitive intelligence.

Lead MSAT activities for internal and external manufacturing partners, managing tech transfers, process validation, deviations/CAPAs, change controls, and lifecycle management. Supervise and mentor MSAT staff, collaborate with Quality, Manufacturing, Regulatory and Supply Chain, support audits/inspections, and drive process robustness and continuous improvement in a cGMP-regulated radiopharmaceutical environment.

Develops and executes territory business plans to grow PYLARIFY adoption across nuclear medicine and imaging centers. Responsibilities include contracting, account management, customer onboarding, product education, stakeholder engagement, reimbursement support, market analysis, and collaboration with sales, medical, marketing, market access, supply chain, and pharmacy manufacturing teams. The role requires strong clinical acumen, negotiation skills, sales analytics, compliance, and up to 60% overnight travel.

Lead regional clinical application efforts for radiopharmaceutical products by building KOL/HCP relationships, providing training and technical expertise, supporting field research and clinical trials, ensuring regulatory compliance, and representing the company at scientific meetings.

Lead and improve order-to-cash systems and processes, supporting SAP S/4HANA OTC modules, integrations (APIs/EDI), and vendor partnerships. Drive KPI-based performance, root-cause analysis, process improvements, compliance (GDP, SOX), issue resolution, reporting, and cross-functional coordination for billing, revenue integrity, and new product/system launches.

Oversee and administer corporate document control within Quality Systems, managing lifecycle of controlled GxP documents in TrackWise Digital. Support eDMS projects, validation, migrations, inspections/audits, training, metrics, remediation, and process improvements while ensuring regulatory compliance and governance across global sites.

Leads health economics and outcomes research strategy for prostate franchise and pipeline products. Oversees HEOR study design, secondary database analyses, pharmacoeconomic modeling, literature reviews, evidence synthesis, stakeholder collaboration, publications, and value-narrative development. Partners with Commercial, Marketing, Market Access, Medical Affairs, and R&D teams to support product strategy and FDA-compliant field materials. Manages budgets, timelines, external experts, and multiple projects while providing HEOR thought leadership. This is a remote U.S. position requiring 25–30% travel.

Lead the biostatistics function for clinical development, define statistical strategies and study designs, oversee programming and CRO deliverables, author SAPs and regulatory statistical sections, ensure CDISC-compliant submissions, mentor staff, allocate resources, and collaborate cross-functionally to support clinical trials and regulatory filings.

Lead market access strategy and execution for major IDNs, academic centers, and large groups to secure coverage, coding, reimbursement, and site setup for current and upcoming radiopharmaceutical products. Build senior relationships, resolve reimbursement issues, drive pull-through, execute educational programs, run business reviews, and collaborate cross-functionally to support patient access and product launches. Field-based with significant travel.

The Market Access Director will lead access strategies for Lantheus' products, build relationships with key accounts, and drive brand growth through education and collaboration with health systems and payers.

Lead regional customer experience for Lantheus radiopharmaceutical products across the Mid-Atlantic. Coordinate daily dose availability, logistics, and supply; liaise with PMFs, sales, and logistics partners; track performance metrics; resolve customer complaints; recommend process and capacity solutions; support launch readiness and cross-functional initiatives to optimize product distribution and customer satisfaction.

Lead market access efforts with referring providers, IDTFs and non-national hospitals to secure and protect access for current and upcoming radiopharmaceutical products. Implement and monitor payer strategies, support site setup for product adoption, engage key decision-makers, track payer policy and market conditions, and collaborate cross-functionally to drive reimbursement and access.

Lead commercial analytics for Cardiology & NETs franchises, delivering performance insights, forecasts, and data-driven recommendations. Partner cross-functionally to execute advanced analytics, build dashboards (PowerBI/Tableau), synthesize findings into strategic narratives, and support commercial decision-making.

Lead regional market access activities for Lantheus by partnering with providers, IDTFs, and non-national hospitals to secure and protect access. Implement market access strategies, support site setup for new product launches (including radioligand therapy), monitor payer policy, coverage, coding and payment, engage decision-makers, and drive pull-through. Field-based role requiring independent work and extensive travel.

Support daily QC lab operations including sample tracking, inventory, equipment management, QC materials, and regulatory compliance (GMP/GLP/OSHA). Coordinate vendors, track KPIs, support stability and inspection readiness, and partner with Quality, Operations, and Facilities to improve workflows and lab services.

Lead commercial partnership strategy and channel relationships for radiopharmaceutical PET manufacturing and distribution. Negotiate contracts, drive partner performance, support product launches, analyze channel performance, and collaborate cross-functionally to achieve strategic and financial goals while ensuring regulatory and operational alignment.

Lead market access efforts for radiopharmaceuticals in the Mid-Atlantic: engage providers and imaging centers, secure and protect payer access, support site setup and patient referral/hub processes, monitor payer policy, and collaborate cross-functionally to execute territory business plans and resolve reimbursement issues.

Manage supplier quality lifecycle for domestic and international suppliers (CMOs, APIs, raw materials, 3PLs). Serve as primary contact for 3PL/pharma partners, oversee supplier performance, lead supplier qualification/onboarding, handle deviations and CAPAs, support supplier change control, audits, and metrics reporting, and drive continuous improvement to maintain compliant vendor management and supply risk mitigation.

Lead clinical study design, protocol development, and interpretation through IND to registration. Serve as clinical lead across cross-functional teams, author key study and regulatory documents, oversee study execution and safety reporting, engage investigators and KOLs, support publications and advisory meetings, and drive clinical strategy for radiopharmaceutical and oncology programs.