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AbbVie
AbbVie
H1B vizasi homiysiIshlab chiqarishKonsaltingSog‘liqni saqlash
AbbVie murakkab sog‘liq muammolari uchun dori vositalarini kashf etish, ishlab chiqish va yetkazib berishga e’tibor qaratadigan global farmatsevtika kompaniyasidir. Uning portfeli immunologiya, onkologiya, nevrologiya va estetika yo‘nalishlarini qamrab oladi, faoliyati esa 175 dan ortiq mamlakatdagi bemorlarga xizmat ko‘rsatadi. Kompaniya faoliyati farmatsevtika tadqiqotlari, ishlab chiqarish va sog‘liqni saqlash sohasidagi tajribani birlashtiradi hamda ilmiy innovatsiyalar va tadqiqotlar hamda ishlanmalarga kiritiladigan katta investitsiyalar bilan qo‘llab-quvvatlanadi. AbbVie sog‘liq natijalari va jamiyatga ta’sirni yaxshilashga qaratilgan kengroq yondashuvining bir qismi sifatida xilma-xillik, barqarorlik va bemorlarni qo‘llab-quvvatlashni ham ta’kidlaydi.
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Kompaniyadagi ish o‘rinlari

Remote Clinical Research Associate II, Oncology at AbbVie

Support AbbVie’s oncology clinical trials through site monitoring, investigator collaboration, and risk management. Help maintain data integrity, recruitment, compliance, and patient safety across trial activities.

USAmerika Qo‘shma ShtatlariKYKentukkiOHOgayo
78 500 $ – 141 000 $ / yil
MasofaviyTo‘liq stavkaJuniorO‘rta darajaDiplom talab qilinmaydiTalab Qilinadigan Til: inglizchaKlinik tadqiqot
Google Cloud Platform

Tavsif

  • Advance AbbVie’s clinical development pipeline through high-quality clinical research
  • Act as the primary contact for investigative sites
  • Provide clinical trial context and connect internal stakeholders with investigative sites
  • Align, train, and motivate site staff and principal investigators on trial objectives, protocols, and patient treatment principles
  • Perform site evaluation, training, routine monitoring, and closeout activities
  • Maintain compliance with protocols, monitoring plans, regulations, GCPs, ICH Guidelines, SOPs, and quality standards
  • Create and tailor strategies for engaging investigative sites
  • Collect site insights and use CRM tools to monitor progress and assess impact
  • Support trial execution by translating protocols and scientific principles into daily activities
  • Assess recruitment and retention approaches in relation to the patient disease journey
  • Build knowledge of therapeutic areas, assets, the clinical landscape, and patient journeys
  • Mentor and train junior CRAs and contribute development feedback
  • Contribute to global and local task forces and initiatives
  • Perform ongoing risk assessments with the Central Monitoring team
  • Address site risk signals and implement preventive and corrective action plans
  • Identify and assess prospective investigators and investigative sites
  • Protect data quality, timely data submission, safety-event reporting, and required follow-up
  • Maintain readiness for audits and regulatory inspections
  • Administer investigator payments in line with executed contract obligations, where applicable

Talablar

  • At least one year of clinically related experience
  • At least six months of clinical research monitoring experience in investigational drug or device trials
  • Familiarity with risk-based monitoring, including onsite and offsite monitoring
  • Knowledge of relevant therapeutic-area indications is preferred
  • Advanced knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies
  • Strong ability to collaborate across functions
  • Strong planning and organizational capabilities
  • Ability to work effectively in a dynamic environment with competing projects and deadlines
  • Ability to use technology, tools, and available resources effectively
  • Strong interpersonal, written, verbal, active-listening, and presentation skills
  • Ability to build site relationships and trusted partnerships
  • Critical-thinking skills and sound judgment when addressing clinical site issues
  • Integrity aligned with AbbVie’s code of business conduct and leadership values
  • Self-motivated approach with focus on timely, high-quality outcomes
  • A relevant tertiary qualification in a health-related field such as medical, scientific, or nursing is preferred

Imtiyozlar

  • Paid vacation, holiday, and sick leave
  • Medical, dental, and vision insurance
  • 401(k) retirement plan
  • Eligibility for short-term incentive programs
  • Equal opportunity employer
  • Reasonable accommodation is available for applicants in the United States and Puerto Rico

O‘xshash ish o‘rinlari

Vision RT Ltd

Field Service Engineer, IT Systems

Vision RT Ltd
201 – 500 Xodimlar
Malakali ishchi vizasi homiysiIshlab chiqarishSog‘liqni saqlashTibbiy sug‘urta
MYMalayziya
100 000 RM – 150 000 RM / yil
GibridTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaDala muhandisi
DNSKiberxavfsizlikSQLTarmoqlararo ekranlar

Install and support Vision RT radiation therapy systems at customer sites across ASEAN. Troubleshoot Windows, networking, hardware, and clinical deployment issues, with frequent travel.

Ochish
Navitus Health Solutions

IT Support Engineer, Madison, WI (Onsite)

Navitus Health Solutions
1 001 – 5 000 Xodimlar
KonsaltingSog‘liqni saqlashSug‘urta
USAmerika Qo‘shma ShtatlariWIViskonsin
54 236 $ – 64 567 $ / yil
OfisdaTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaQo‘llab-quvvatlash muhandisi

Support Navitus data center facilities, hardware, software, and infrastructure in an onsite IT role. Provide advanced technical assistance, troubleshoot issues, coordinate upgrades, and participate in rotating on-call coverage.

Ochish