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Regeneron
Regeneron
H1B vizos rėmėjasBiotechnologijaGamybaSveikatos priežiūra
„Regeneron“ yra biotechnologijų bendrovė, atrandanti, kurianti ir komercializuojanti vaistus sunkioms ir nepakankamai gydomoms ligoms. Jos tyrimai apima alergijas, širdies ir kraujagyslių bei medžiagų apykaitos ligas, neuromokslą, onkologiją, hematologiją, oftalmologiją ir retąsias ligas. Derindama biologinius tyrimus su pažangiomis technologijomis, „Regeneron“ kuria biologinius ir genetinius vaistus, skirtus sudėtingiems sveikatos priežiūros poreikiams spręsti. Siekdama gerinti pacientų priežiūrą, bendrovė taip pat pabrėžia sveikatos lygybę, atsakomybę už aplinką, mokslinį švietimą ir etišką verslo praktiką.
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Clinical Study Specialist at Regeneron

Support Regeneron clinical trial teams by coordinating study data, sites, reporting, and close-out activities. Help keep studies on track from site activation through completion.

USJungtinės ValstijosMAMasačusetsasNJNaujasis DžersisNYNiujorkas
93 900 $ – 153 300 $ / metai
HibridinisVisas etatasJaunesnysis specialistasVidutinis lygisPrivaloma Kalba: anglųBendraKlinikinis specialistas
Google Cloud Platform

Aprašymas

  • Support clinical study teams with technical and administrative work across trial programs.
  • Help keep studies on schedule from site activation through close-out.
  • Prepare reports and metrics in formats suitable for analysis.
  • Coordinate study team meetings, including agendas and minutes.
  • Compile information for feasibility reviews and site selection.
  • Assist with reviewing study documents and reference materials.
  • Monitor site activation, enrollment, and monitoring visits against plans.
  • Raise issues and delays, and track investigator and site status as well as registry postings.
  • Follow up on scheduled reports and reconcile trial master files with guidance from the study lead.
  • Contact sites as directed and maintain site details and working relationships.
  • Assist with study close-out and support oversight of external vendors.
  • Assess how new information may affect ongoing trials.
  • Take part in standard operating procedure updates and departmental initiatives.
  • Suggest ways to improve processes.

Reikalavimai

  • Bachelor’s degree and at least two years of industry-related clinical experience.
  • Ability to develop working knowledge of trial management systems and Microsoft applications, including Project, PowerPoint, Word, and Excel, as well as 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.

Privalumai

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

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The Nursing and Midwifery Council

Education Data Analyst – The Nursing and Midwifery Council

The Nursing and Midwifery Council
501 – 1 000 Darbuotojai
Ne pelno organizacijosSveikatos draudimasSveikatos priežiūra
GBJungtinė Karalystė
40 982 £ – 48 961 £ / metai
HibridinisVisas etatasVidutinis lygisVyresnysis specialistasPrivaloma Kalba: anglųDuomenų analitikas

Turn complex data into dashboards and practical insight to support the Nursing and Midwifery Council’s education quality assurance and regulatory decisions across the UK.

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