Own site-level clinical supply chain operations for late-stage and Phase III trials, resolving delivery and product issues while coordinating partners and improving supply reliability to support uninterrupted patient treatment.
Telixus jobs
A company focused on helping patients with cancer live longer with better quality of life.
55 open roles at Telixus
Leads clinical quality oversight for clinical trials, planning and conducting GCP, GVP, and GCLP audits, supporting regulatory inspections, and strengthening compliance across early- and late-stage programs.
Leads US medical affairs execution for renal cancer theranostics, shaping medical strategy, launch readiness, and lifecycle planning while translating emerging evidence into cross-functional plans and scientific engagement.
Leads US medical affairs execution for prostate cancer theranostics, shaping medical strategy, launch readiness, evidence generation, scientific communications, and cross-functional collaboration.
Leads global clinical trial planning and execution across programs, ensuring timelines, budgets, quality, and regulatory compliance while managing CROs, cross-functional teams, and staff development.
Leads a portfolio of strategic and operational improvement initiatives, shaping governance, investment decisions, and cross-functional execution while advising senior leaders and driving measurable business impact.
Lead legal counsel for Americas commercial and medical affairs, advising across the pharmaceutical product lifecycle on regulatory promotion, healthcare compliance, market access, contracting, and disputes.
Provides day-to-day legal support for Telix Manufacturing Solutions by negotiating manufacturing and supply contracts, advising on quality and regulatory issues, and improving contracting processes.
Leads technology transfers and manufacturing facility deployments for diagnostic and therapeutic products, coordinating readiness, qualification, validation, documentation, and regulatory approval through handoff to operations.
Leads Quality Assurance oversight of commissioning, qualification, and validation across manufacturing sites, ensuring GMP compliance, inspection readiness, and transition from project execution to routine operations.
Leads QC laboratory startup and readiness across manufacturing sites, overseeing analytical method development and validation, equipment qualification, GMP compliance, investigations, and inspection readiness.
Maintains and troubleshoots cyclotrons, chemistry modules, and analytical equipment while supporting radiopharmaceutical production and quality control in compliance with safety and regulatory standards.
Manage cross-functional business improvement initiatives from planning through execution, using analysis, structured project management, and stakeholder coordination to keep work on track and support informed decisions.
Leads biologics process development and clinical manufacturing across analytical, purification, formulation, and bioconjugation work, coordinating internal teams and CMC partners while supporting quality and regulatory requirements.
Coordinate integrated digital and content marketing campaigns, managing platform deployment, channel assets, tracking, reporting, and event communications to support accurate execution and measurable performance.
Leads national and global clinical trials from protocol development through closeout, managing study teams, vendors, budgets, quality, risks, and deliverables across complex clinical research programs.
Leads national account growth across Urology and Community Oncology, developing strategic partnerships, negotiating complex contracts, and aligning regional and cross-functional teams to deliver revenue and corporate objectives.
Lead business development across assigned specialty networks, building strategic partnerships and coordinating cross-functional resources to grow oncology diagnostic and therapeutic solutions and exceed corporate goals.
Drive territory sales growth for radiopharmaceutical products by developing new business, managing healthcare accounts, delivering clinical product education, and using market and sales data to improve performance.
Lead CMC strategy and cross-functional execution for Illuccix and Gozellix, coordinating manufacturing partners, regulatory readiness, budgets, risks, and lifecycle activities from development through commercialization.
Lead CMC strategies and cross-functional execution for Illuccix and Gozellix, coordinating manufacturing partners, regulatory readiness, budgets, risks, and lifecycle activities from development through commercialization.
Leads global investigational product labeling across clinical development, ensuring compliant, accurate labeling and coordinating cross-functional reviews, translations, artwork, documentation, and regulatory support.
Manage clinical trial supply chain activities, coordinating procurement, inventory, vendors, and global shipments to ensure materials reach study sites on time and meet regulatory requirements.
Leads regulatory review and compliance for advertising, promotion, and disease-awareness materials across global markets, advising cross-functional teams and coordinating submissions for investigational and commercial products.
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