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BeOne Medicines
BeOne Medicines
BiotexnologiyaFarmatsevtika mahsulotlariSog‘liqni saqlash
BeOne Medicines — bosh qarorgohi Shveytsariyada joylashgan, saraton kasalligini davolash usullarining hamyonbopligi va mavjudligini yaxshilashga qaratilgan innovatsion davolash vositalarini kashf etish va ishlab chiqishga ixtisoslashgan global onkologiya kompaniyasi. Uning portfeli gematologik saratonlar va qattiq o‘smalarni qamrab oladi. Portfel kompaniyaning ichki imkoniyatlari hamda tashqi hamkorliklar orqali rivojlantirilayotgan yangi terapevtik vositalarning kengayib borayotgan ishlab chiqish yo‘nalishi bilan qo‘llab-quvvatlanadi. Olti qit’ada 11 000 dan ortiq xodimga ega BeOne Medicines butun dunyo bo‘ylab bemorlarning dori-darmonlardan foydalanish imkoniyatini kengaytirish ustida ishlamoqda.
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Kompaniyadagi ish o‘rinlari

Regional Clinical Study Manager - United States Remote

Lead regional oncology clinical trial delivery for BeOne Medicines across timelines, sites, vendors, budgets, compliance, and operational teams. Oversee study execution from feasibility through closeout while maintaining quality and inspection readiness.

USAmerika Qo‘shma Shtatlari
136 400 $ – 181 400 $ / yil
MasofaviyTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaKlinik tadqiqot
Google Cloud Platform

Tavsif

  • Own regional study delivery to quality, timeline, budget, and inspection-readiness standards
  • Serve as regional lead for multiple studies within an indication or program
  • Direct regional clinical operations teams and external regional partners
  • Act as the escalation contact for regional study challenges
  • Coordinate regional deliverables with overarching study objectives
  • Create regional tools, work instructions, and standard operating procedures
  • Plan and manage regional clinical studies from feasibility through closeout
  • Oversee study start-up and recruitment milestones and monitor progress
  • Lead trial feasibility assessments, country allocation, and site selection
  • Coordinate local updates to global study documents and regulatory or ethics submissions
  • Keep regional and country data current in study systems
  • Partner with CRAs on study execution and monitoring report reviews
  • Oversee creation, maintenance, and quality control of regional and country Trial Master Files
  • Contribute to decisions on clinical supplies, drug inventory, labeling, and comparator status
  • Manage regional data collection, entry, and query resolution
  • Support planning and delivery of Clinical Study Reports
  • Monitor adherence to protocols, SOPs, ICH/GCP, and applicable regulations
  • Maintain inspection readiness and prepare sites for audits and inspections
  • Lead quality enhancements and communicate effective practices
  • Select and oversee regional vendors
  • Manage regional clinical study budgets
  • Oversee investigator fees, site payments, and patient travel reimbursements
  • Plan regional resource requirements and monitor utilization
  • Provide performance feedback and mentor junior colleagues

Talablar

  • Bachelor’s degree in a scientific or healthcare discipline is required
  • An advanced degree is preferred
  • At least six years of progressive clinical research experience in biotechnology, pharmaceuticals, or a CRO
  • Demonstrated clinical research experience, including team leadership in clinical functions
  • CRA experience is preferred
  • Proficiency with Microsoft Office
  • Proficiency with project planning applications
  • Relevant clinical operations experience may support an exception to the degree requirement
  • Travel may be required based on business needs

Imtiyozlar

  • Eligibility for an annual bonus plan in non-commercial roles
  • Eligibility for an incentive compensation plan in commercial roles
  • Discretionary equity awards
  • Employee Stock Purchase Plan
  • Medical insurance
  • Dental insurance
  • Vision insurance
  • 401(k) plan
  • FSA/HSA
  • Life insurance
  • Paid time off
  • Wellness benefits
  • Reasonable accommodation throughout the application process

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