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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

Global Clinical Study Manager – Remote, United States

Lead global clinical study delivery for BeOne Medicines, coordinating cross-functional teams, vendors, timelines, budgets, quality, and regulatory readiness. This role oversees oncology-focused clinical operations from feasibility through study closeout.

USAmerika Qo‘shma Shtatlari
118 600 $ – 158 600 $ / yil
MasofaviyTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaKlinik tadqiqot
Google Cloud Platform

Tavsif

  • Own global study delivery against approved timelines, budgets, and inspection-readiness standards
  • Direct all activities for assigned clinical studies
  • Lead global cross-functional study teams, oversee external partners, and escalate study issues when needed
  • Align study objectives with clinical operations priorities and corporate goals
  • Manage external vendors and work with regional subject matter experts
  • Provide senior management with regular updates on study progress
  • Represent the study team in internal forums and chair Clinical Study Team meetings
  • Direct study planning and execution from feasibility through closeout
  • Develop, maintain, and communicate comprehensive study timelines
  • Oversee regional trial feasibility, allocation, and site selection
  • Ensure study documents are available on time for regulatory and ethics submissions
  • Manage study start-up activities and site activation plans
  • Ensure study plans, systems, and tools are established, implemented, and maintained
  • Apply risk-based quality management and centralized monitoring analyses
  • Create study-specific training, deliver it as needed, and maintain training records
  • Create, maintain, and quality-check the Trial Master File
  • Forecast study drug demand and coordinate timely supply deliveries to sites
  • Support data-cleaning milestones with Data Management and other stakeholders
  • Plan and deliver the Clinical Study Report with Medical Writing and study team contributors
  • Monitor adherence to protocols, SOPs, study plans, ICH/GCP, and applicable regulations
  • Review quality metrics and sustain inspection readiness
  • Identify study issues and ensure corrective and preventive actions are completed
  • Report risks and challenges to senior management and implement mitigation strategies
  • Prepare study teams for quality assurance audits and inspections
  • Share lessons learned and effective practices across teams and sites
  • Lead process improvements and contribute to work instructions and SOPs
  • Select and oversee study vendors and approve invoice payments
  • Manage study budgets, change control, closeout budgets, accruals, and forecasts
  • Assess study staffing needs and monitor resource utilization
  • Keep studies within approved time, quality, and cost parameters

Talablar

  • Demonstrated project management experience across global clinical studies
  • Oncology experience is preferred
  • Advanced knowledge of clinical operations methods and practices
  • Thorough understanding of end-to-end clinical study processes
  • Capability to independently lead global clinical studies
  • At least six years of progressively responsible clinical research experience in biotech, pharmaceutical, or CRO organizations
  • Proficiency with Microsoft Office
  • Experience using project planning software
  • Experience with Clinical Trial Management Systems
  • Bachelor’s degree in a scientific or healthcare field required; an advanced degree is preferred
  • Willingness to travel when business needs require

Imtiyozlar

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

O‘xshash ish o‘rinlari

AT&T

AT&T Business Sales Representative, Territory Accounts — Memphis

AT&T
H1B vizasi homiysiTelekommunikatsiyalarTexnologiya va innovatsiya
USAmerika Qo‘shma ShtatlariTNTennessi
38 800 $ – 58 200 $ / yil
OfisdaTo‘liq stavkaJuniorO‘rta darajaDiplom talab qilinmaydiTalab Qilinadigan Til: inglizchaSotuv

Build AT&T’s Memphis small-business and mid-market customer base by selling fiber broadband and other communications solutions. The role combines prospecting, account development, and consultative selling to grow territory revenue.

Ochish