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Telix Pharmaceuticals Limited
Telix Pharmaceuticals Limited
501 – 1 000 Darbuotojai
BiotechnologijaKonsultavimasSveikatos priežiūra

Telix Pharmaceuticals Limited yra komercinės veiklos etapą pasiekusi biofarmacijos įmonė, kurianti ir komercializuojanti teranostinius radiofarmacinius preparatus vėžiui ir retoms ligoms gydyti. Jos požiūris apima tikslinį vaizdinimą ir spinduliuote pagrįstą gydymą, kad būtų galima priimti geriau informuotus klinikinius sprendimus ir taikyti individualizuotą priežiūrą.

Įmonės kuriamų produktų programa apima prostatos ir inkstų vėžį, neuroonkologiją bei judamojo aparato vėžinius susirgimus. Telix gavo pasaulinius reguliavimo institucijų patvirtinimus pagrindiniam vaizdinimo produktui „Illuccix®“ ir toliau plėtoja plačią klinikinių tyrimų programą visame pasaulyje. Jos komanda dirba sveikatos priežiūros, biotechnologijų ir susijusiose komercinėse srityse, kad radiofarmacinės inovacijos iš kūrimo etapo pasiektų klinikinį taikymą.

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Darbai įmonėje

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.

USJungtinės ValstijosNuotolinisVisas etatasVyresnysis specialistasPrivaloma Kalba: anglųKlinikinės operacijos
Google Cloud PlatformPMP

Aprašymas

  • 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.

Reikalavimai

  • 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.

Privalumai

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

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