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Ora
Ora
201 – 500 Xodimlar
H1B vizasi homiysiIshlab chiqarishKonsaltingLogistika
Ora dastlabki bosqichdagi kompaniyalardan tortib global farmatsevtika va tibbiy qurilmalar tashkilotlarigacha bo‘lgan innovatorlarni qo‘llab-quvvatlovchi, oftalmologik dori vositalari va qurilmalarini ishlab chiqish bo‘yicha to‘liq xizmat ko‘rsatuvchi kompaniyadir. Uning jamoalari 45 yildan ortiq vaqt davomida oftalmologik mahsulotlarni klinikagacha va klinik ishlab chiqish bosqichlarida ilgari surishga, integratsiyalashgan klinik ma’lumotlar yechimlari, ixtisoslashtirilgan metodologiyalar va global tartibga solish strategiyasi bilan ta’minlashga yordam berib kelmoqda. Ora Amerika Qo‘shma Shtatlari, Buyuk Britaniya, Avstraliya va Osiyodagi xalqaro ofislaridan amalga oshiriladigan loyihalarda oftalmologiya mutaxassislari, tadqiqot va ishlab chiqish bo‘yicha professionallar hamda tajribali rahbarlarni birlashtiradi. Kompaniya faoliyati mijozlarga ko‘rish salomatligi uchun yangi mahsulotlarni ishlab chiqish va mahsulot tashabbuslarining imkoniyatlarini maksimal darajada oshirishga yordam berishga qaratilgan.
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Kompaniyadagi ish o‘rinlari

Clinical Operations Manager - Ora (United States Remote)

Lead Clinical Trial Associate operations at Ora, an ophthalmic drug and device development company. Drive compliant trial execution, inspection readiness, team performance, and continuous process improvement.

USAmerika Qo‘shma ShtatlariMasofaviyTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaKlinik operatsiyalar
Google Cloud PlatformVault

Tavsif

  • Lead Clinical Trial Associate operations and serve as the subject matter expert within Clinical Monitoring
  • Work with leadership to execute operational strategies, department goals, and process improvements
  • Forecast resources and assess workloads across the CTA team
  • Provide functional leadership, mentoring, guidance, and daily support to CTA staff
  • Support CTA onboarding, training, and career development
  • Review and approve time records and expenses for direct reports
  • Escalate and resolve CTA operational matters with Monitoring leadership
  • Coordinate with Project Managers, CTMs, and CRAs to align CTA work with study plans and timelines
  • Track CTA performance measures and operational metrics
  • Contribute to inspection readiness and audit preparation
  • Oversee CTA deliverables to support quality and compliance
  • Lead standardization, optimization, automation, and continuous improvement efforts
  • Help create and maintain SOPs, work instructions, training content, and operational tools
  • Encourage effective adoption of CTMS, eTMF, and other clinical systems
  • Assess operational risks and recommend corrective solutions
  • Oversee CTA support across study startup, maintenance, and closeout
  • Ensure study records and TMF activities are complete and ready for inspection
  • Support adherence to sponsor requirements, SOPs, ICH-GCP, and applicable regulations
  • Provide additional project support when junior staff oversight or extra resources are needed

Talablar

  • Bachelor’s degree and five years of clinical research experience, or an equivalent combination of education, training, and experience; relevant experience may substitute for education
  • At least one year of management or leadership experience, ideally in a CRO environment
  • Strong clinical operations experience, preferably with Ora processes and tools including Veeva Vault eTMF and CTMS, ICH-GCP, the DIA TMF Reference Model, and regulatory guidance
  • Demonstrated experience leading cross-functional teams and mentoring junior clinical operations staff
  • Previous CRO experience is strongly preferred
  • Ability to motivate, lead, and mentor team members while identifying coaching opportunities
  • Working knowledge of regulatory requirements and their impact on clinical operations
  • Experience managing relationships with sites, vendors, sponsors, and other external partners
  • Detailed understanding of clinical trial documentation, records management, and ICH-GCP requirements
  • Extensive experience supporting ophthalmology clinical trials
  • Ability to work independently, take initiative, and deliver work on schedule
  • Strong communication skills for collaborating with internal teams, sponsors, and vendors, including escalation, training, and issue response
  • Ability to set objectives, build structure, and maintain a focused, collaborative approach to high-quality work

Imtiyozlar

  • Medical, dental, and vision coverage available from the first day
  • Flexible paid time off
  • Unlimited sick leave
  • 14 company-paid holidays
  • Fidelity 401(k) plan with company matching
  • Adoption assistance
  • Fertility assistance
  • 16 weeks of paid parental leave
  • Company-paid life insurance
  • Company-paid disability insurance
  • Remote workspace reimbursement
  • Wellness reimbursement
  • Employee Assistance Program
  • Career development opportunities
  • Collaboration with colleagues around the world

O‘xshash ish o‘rinlari

Bloomlife Inc

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Illumina

Clinical Sales Specialist, Genomics — Thailand, Indonesia and Vietnam

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5 001 – 10 000 Xodimlar
H1B vizasi homiysiIshlab chiqarishKonsaltingSog‘liqni saqlash
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Trane Technologies
B2BEnergetikaIshlab chiqarish
USAmerika Qo‘shma ShtatlariMNMinnesotaNCShimoliy Karolina
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GibridTo‘liq stavkaSeniorYetakchiTalab Qilinadigan Til: inglizchaRahbar yordamchisi

Support Trane Technologies’ Digital leadership team by coordinating executive schedules, travel, meetings, communications, and procurement. The role covers leaders across the United States and requires on-site work in White Bear Lake, Minnesota, Monday through Thursday.

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GlobeLife

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GlobeLife
1 – 10 Xodimlar
FanSog‘liqni saqlashTa’lim
USAmerika Qo‘shma ShtatlariMasofaviyTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaMijozlar muvaffaqiyatiMijozlarni saqlab qolish bo‘yicha mutaxassis

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