Jobs at Lantheus

Develop and execute territory business plans to drive sales of DEFINITY cardiology products. Build relationships with healthcare stakeholders, communicate clinical and economic value, provide reimbursement support, educate cardiology programs, manage contracting, and collaborate with marketing, medical affairs, and sales teams. The role requires customer engagement, overnight travel, facility credentialing, and compliance with company and healthcare standards.

Lead enterprise automation architecture and delivery across RPA, workflow automation, process mining, intelligent automation, testing, bots, citizen development, and AI orchestration. Establish and operate an Automation Center of Excellence, identify high-value use cases, guide implementation, manage governance and regulatory alignment, support training and adoption, and track financial value. Work hands-on with business stakeholders, technology teams, vendors, and external consultants in a regulated life sciences environment.

Leads enterprise strategy, architecture, delivery, governance, and operations across data, analytics, information management, automation, AI, and GenAI. Drives transformation toward governed data foundations, reusable data products, data marketplaces, self-service analytics, and responsible AI. Oversees platforms, pipelines, dashboards, automation initiatives, budgets, vendors, and senior technical teams while partnering with business, Legal, Compliance, Quality, and Security. Builds training, adoption, stewardship, and change-management programs across a global life sciences organization.

Leads regional clinical application efforts for radiopharmaceutical products across a multi-state territory. Builds relationships with healthcare providers and key opinion leaders, delivers training on product handling, administration, infusion, licensing, and radiation safety, and provides scientific support for approved and investigational products. Supports field research, clinical trials, investigator-sponsored studies, congresses, and medical booth activities while maintaining regulatory and company compliance. This remote role requires 60% travel and residence near an international airport.

Leads enterprise integration and data readiness architecture, implementation, governance, and enablement. Designs data lakes, warehouses, lakehouses, data products, marketplaces, semantic layers, and AI-ready data assets using platforms including Informatica, Databricks, Snowflake, and SAP. Drives data quality, lineage, security, privacy, MDM, self-service analytics, reporting, natural-language querying, training, and organizational adoption. Provides hands-on technical leadership, delivery oversight, prioritization, mentoring, technology evaluation, and value realization across business functions.

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 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 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.

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.