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Regeneron
Regeneron
H1B vizasi homiysiBiotexnologiyaIshlab chiqarishSog‘liqni saqlash
Regeneron jiddiy va tibbiy ehtiyojlari yetarlicha qondirilmagan kasalliklarga qarshi dori vositalarini kashf etadigan, ishlab chiqadigan va tijoratlashtiradigan biotexnologiya kompaniyasidir. Uning tadqiqotlari allergiya, yurak-qon tomir va metabolik kasalliklar, neyrofan, onkologiya, gematologiya, oftalmologiya hamda kam uchraydigan kasalliklarni qamrab oladi. Regeneron biologik tadqiqotlarni ilg‘or texnologiyalar bilan birlashtirib, murakkab tibbiy ehtiyojlarni qondirishga mo‘ljallangan biologik preparatlar va genetik dori vositalari ustida ishlaydi. Kompaniya bemorlarga ko‘rsatiladigan yordamni rivojlantirishga qaratilgan kengroq missiyasining bir qismi sifatida sog‘liqni saqlashdagi tenglik, atrof-muhitga mas’uliyat, ilmiy ta’lim va axloqiy korporativ amaliyotlarni ham ta’kidlaydi.
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Kompaniyadagi ish o‘rinlari

Clinical Study Specialist

Support clinical trial operations at Regeneron, a medicines developer, by tracking study progress, documentation, sites, vendors, and close-out work.

USAmerika Qo‘shma ShtatlariNJNyu-JersiNYNyu-York
93 900 $ – 153 300 $ / yil
GibridTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaKlinik mutaxassisUmumiy
Google Cloud Platform

Tavsif

  • Prepare clear reports and study metrics for analysis.
  • Arrange study team meetings and prepare agendas and minutes.
  • Compile information for feasibility reviews and site selection.
  • Help review study documents and reference materials.
  • Monitor site activation, enrollment, and monitoring visits against plans.
  • Raise issues and delays, and track investigator and site status and registry postings.
  • Follow up to ensure scheduled reports arrive on time.
  • Reconcile trial master files with guidance from the study lead.
  • Communicate with study sites and maintain contact details and working relationships.
  • Assist with study close-out activities.
  • Help oversee third-party vendors when needed.
  • Assess how new information may affect ongoing trials.
  • Take part in standard operating procedure updates and departmental initiatives.
  • Suggest ways to improve processes.

Talablar

  • Bachelor’s degree and at least two years of industry-related experience in a clinical setting.
  • Ability to develop working knowledge of trial management systems and Microsoft applications, including Project, PowerPoint, Word, Excel, IVRS/IWRS, EDC, and TMF.
  • Basic familiarity with medical terminology and clinical drug development.
  • Awareness of ICH/GCP.
  • Proactive and self-disciplined, with the ability to manage deadlines and priorities effectively.

Imtiyozlar

  • Annual bonuses or other incentive plans.
  • Equity awards.
  • Pension or retirement benefits.
  • 401(k) with a company match.
  • Health and wellness programs.
  • Fitness centers.
  • Medical, dental, vision, life, and disability insurance.
  • Paid time off.
  • Family support benefits.
  • Hybrid work flexibility.
  • Reasonable accommodations during recruitment where required.

O‘xshash ish o‘rinlari

Terumo Medical Corporation

Region Manager, Terumo Interventional Systems Sales

Terumo Medical Corporation
1 001 – 5 000 Xodimlar
H1B vizasi homiysiIshlab chiqarishKonsaltingSog‘liqni saqlash
USAmerika Qo‘shma ShtatlariNJNyu-Jersi
120 000 $ – 165 000 $ / yil
OfisdaTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaMenejer

Lead medical device sales across a North Central New Jersey region, managing field teams and hospital relationships. Drive regional revenue, sales performance, and compliant promotion of Terumo Interventional Systems products.

Ochish