Regeneron
Regeneron
Regeneron — күрделі әрі жеткілікті деңгейде қанағаттандырылмаған медициналық қажеттіліктерге арналған дәрі-дәрмектерді ашатын, әзірлейтін және нарыққа шығаратын биотехнологиялық компания. Оның зерттеулері аллергия, жүрек-қантамыр және метаболизм аурулары, нейроғылым, онкология, гематология, офтальмология және сирек кездесетін аурулар бағыттарын қамтиды. Regeneron биологиялық зерттеулерді озық технологиялармен ұштастыра отырып, күрделі медициналық қажеттіліктерді шешуге арналған биологиялық препараттар мен генетикалық дәрілерді әзірлейді. Компания пациенттерге көрсетілетін көмекті жетілдіруге бағытталған кең ауқымды миссиясының бір бөлігі ретінде денсаулық сақтау саласындағы теңдікті, қоршаған ортаға жауапкершілікті, ғылыми білім беруді және этикалық корпоративтік тәжірибені де атап көрсетеді.

Clinical Study Specialist

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

Сипаттама

  • 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.

Талаптар

  • 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.

Артықшылықтар

  • 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.

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