LogoFresh Jobs Ahead
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.
LinkedIn
Kompaniyadagi ish o‘rinlari

Clinical Research Associate II, China (Remote)

Support AbbVie’s immunology clinical trials through investigative-site monitoring, regulatory compliance, data-quality oversight, and patient-safety activities.

CNXitoyMasofaviyTo‘liq stavkaJuniorO‘rta darajaDiplom talab qilinmaydiTalab Qilinadigan Til: inglizchaKlinik tadqiqot
Google Cloud Platform

Tavsif

  • Advance AbbVie’s clinical research pipeline through high-quality research execution and effective use of available capabilities
  • Collaborate with investigators and site teams to build productive clinical-trial relationships
  • Act as the primary contact for investigative sites
  • Share relevant trial information and connect stakeholders with investigative sites
  • Train, align, and motivate site staff and principal investigators on trial objectives, protocols, and patient-treatment principles
  • Perform site selection, initiation training, routine monitoring, and close-out monitoring in accordance with protocols, regulations, GCP, ICH guidelines, SOPs, and quality standards
  • Tailor site-engagement plans, collect local insights, and use CRM tools to track progress and evaluate impact
  • Translate study protocols, scientific concepts, and trial requirements into effective day-to-day execution
  • Assess recruitment and retention approaches in the context of the patient disease journey
  • Build knowledge of therapeutic areas, assets, the clinical landscape, and patient journeys to support recruitment and protocol adherence
  • Coach less experienced CRAs and contribute to their development
  • Contribute to global and local task forces and initiatives
  • Work with the Central Monitoring team on ongoing risk assessments to identify study-performance and patient-safety concerns
  • Address site-risk signals and execute preventive and corrective action plans
  • Identify and assess prospective investigators and investigative sites
  • Ensure site data is submitted accurately and on schedule, including safety-event reporting and follow-up
  • Maintain readiness for audits and regulatory inspections
  • Administer investigator payments when applicable

Talablar

  • A relevant tertiary qualification in a health-related field, such as medicine, science, or nursing, is preferred
  • At least one year of clinically related experience, including six months monitoring investigational drug or device trials
  • Experience with risk-based monitoring, including both onsite and remote monitoring
  • Knowledge of the applicable therapeutic-area indications is preferred
  • Advanced understanding of local regulatory and legal requirements, ICH/GCP guidelines, and relevant policies
  • Ability to collaborate effectively with internal and external stakeholders across functions
  • Strong planning and organizational abilities, with the capacity to manage competing projects and deadlines in a changing environment
  • Advanced proficiency in using technology, tools, and resources to provide customer-focused site support
  • Strong interpersonal, written, verbal, active-listening, and presentation skills
  • Ability to build trusted site relationships through effective engagement, motivation, and training
  • Sound critical-thinking and judgment skills for resolving clinical-site issues
  • Commitment to integrity and compliance with AbbVie’s code of business conduct and leadership values
  • Self-directed approach and consistent focus on timely, high-quality results in a fast-paced setting

Imtiyozlar

  • Equal-opportunity employer
  • Commitment to integrity, innovation, transforming lives, and serving the community

O‘xshash ish o‘rinlari

Peraton

Senior Hybrid Connectivity Engineer

Peraton
H1B vizasi homiysiKonsaltingLogistikaSog‘liqni saqlash
USAmerika Qo‘shma ShtatlariVAVirjiniya
112 000 $ – 179 000 $ / yil
OfisdaTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaMuhandis
AWSBulutDNSKiberxavfsizlikKubernetesTarmoqlararo ekranlarTCP/IPTypeScript

Designs and troubleshoots connectivity across AWS classified cloud, Kubernetes, and on-premises networks. Supports Peraton’s national security and government technology missions.

Ochish