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Telix Pharmaceuticals Limited
Telix Pharmaceuticals Limited
501 – 1,000 Employees
BiotechnologyConsultingHealthcare

Telix Pharmaceuticals Limited is a commercial-stage biopharmaceutical company developing and commercializing theranostic radiopharmaceuticals for cancer and rare diseases. Its approach combines targeted imaging with radiation-based treatment to support more informed clinical decisions and personalized care.

The company’s pipeline spans prostate and kidney cancer, neuro-oncology, and musculoskeletal cancers. Telix has secured global regulatory approvals for its lead imaging product, Illuccix®, and continues to advance a broad program of clinical trials worldwide. Its team works across healthcare, biotechnology, and related commercial disciplines to bring radiopharmaceutical innovations from development into clinical use.

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Senior Clinical Project Manager, Remote (United States)

Lead global clinical trials for Telix Pharmaceuticals’ precision radiopharmaceuticals, overseeing study delivery from protocol finalization through closeout. Coordinate vendors, budgets, risks, and cross-functional teams across complex multinational research projects.

USUnited StatesRemoteFull-timeSeniorEnglish RequiredClinical Operations
Google Cloud PlatformPMP

Description

  • Oversee national and global clinical trials from protocol finalization through closeout.
  • Select vendors and sites, assess feasibility, and manage timelines, budgets, resources, and vendor relationships.
  • Forecast spending and identify ways to accelerate work or shift expenditure.
  • Create integrated study management plans with the core project team.
  • Prepare and maintain study documents, including protocols, informed consent forms, and clinical manuals.
  • Track external partners’ quality, timelines, and budget performance.
  • Put effective project plans into operation in line with applicable SOPs.
  • Anticipate and manage risks, leading teams through problem-solving and resolution.
  • Help develop and maintain clinical SOPs and trial processes.
  • Shape project delivery strategies for RFPs and lead bid defense preparation.
  • Direct complex, multinational, multicenter clinical research projects.
  • Create patient recruitment strategies.
  • Negotiate site and vendor contracts and budgets.
  • Update leadership and cross-functional stakeholders on trial progress, issues, and mitigations.
  • Train study team members and mentor clinical project managers.
  • Work independently with limited supervision.
  • Represent clinical operations at medical conferences through investigator engagement and presentations.

Requirements

  • A bachelor’s degree in life sciences is required.
  • PMP certification is preferred.
  • At least five years of relevant clinical trial project management experience is required.
  • Experience with late-phase trials (Phase 3–4 or registration studies), oncology, and/or radiopharmaceuticals is preferred.
  • Strong written and verbal communication, organization, and problem-solving skills, including the ability to meet tight timelines.
  • Collaborative approach and ability to work across functions.
  • Experience managing global clinical trials.
  • Thorough knowledge of ICH Good Clinical Practice (GCP) and regulatory processes.
  • Ability to quickly adjust study strategy and guide teams effectively.
  • Strong analytical, organizational, planning, decision-making, negotiation, and conflict-management skills.
  • Proficiency with Microsoft Office, including Word, Excel, SharePoint, and Teams, and experience working primarily with electronic records.
  • Demonstrated leadership and ability to support others’ development.
  • Study startup experience, including country and site feasibility and ethics and regulatory submissions across multiple regions (APAC, EMEA, and North America).
  • Travel of approximately 10% is expected.

Benefits

  • Competitive salary.
  • Annual performance-based bonuses.
  • Equity-based incentive program.
  • Generous vacation.
  • Paid wellness days.
  • Learning and development support.

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