Regeneron
Regeneron
Regeneron एक जैव-प्रौद्योगिकी कंपनी है जो गंभीर और उपेक्षित स्वास्थ्य समस्याओं के लिए दवाओं की खोज, विकास और व्यावसायीकरण करती है। इसका अनुसंधान एलर्जी, हृदय एवं चयापचय संबंधी रोगों, तंत्रिका-विज्ञान, कैंसर-विज्ञान, रक्त-विज्ञान, नेत्र-विज्ञान और दुर्लभ रोगों तक फैला हुआ है। जैविक अनुसंधान को उन्नत प्रौद्योगिकी के साथ जोड़कर Regeneron जटिल स्वास्थ्य देखभाल आवश्यकताओं को पूरा करने के उद्देश्य से जैविक और आनुवंशिक औषधियों पर काम करती है। रोगी देखभाल को आगे बढ़ाने के अपने व्यापक मिशन के तहत कंपनी स्वास्थ्य समानता, पर्यावरणीय जिम्मेदारी, वैज्ञानिक शिक्षा और नैतिक कॉर्पोरेट प्रथाओं पर भी जोर देती है।

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.

विवरण

  • 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.

आवश्यकताएँ

  • 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.

लाभ

  • 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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