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Asahi Kasei
Asahi Kasei
H1B वीज़ा प्रायोजकखाद्य और पेयनिर्माणस्वास्थ्य सेवा
Asahi Kasei एक जापानी औद्योगिक समूह है, जो सामग्री, रसायन, इलेक्ट्रॉनिक्स, आवास और निर्माण, स्वास्थ्य सेवा तथा औषधि जैसे क्षेत्रों में काम करता है। इसके अनुसंधान और व्यावसायिक संचालन में सेमीकंडक्टर प्रौद्योगिकियाँ, जीवन विज्ञान, चिकित्सा उपकरण और इलेक्ट्रोलिसिस तथा हाइड्रोजन उत्पादन जैसे ऊर्जा समाधान शामिल हैं। कंपनी विभिन्न बाजारों में औद्योगिक विनिर्माण और अनुप्रयुक्त अनुसंधान को जोड़ती है, जबकि स्थिरता और नवाचार इसके कार्य को दिशा देते हैं।
LinkedIn
कंपनी की नौकरियाँ

Senior Clinical Research Associate – Cary, NC (Hybrid)

Support Asahi Kasei’s specialty pharmaceutical trials through centralized site oversight, clinical data review, Trial Master File quality, and CRO monitor performance management.

USसंयुक्त राज्यNCउत्तरी कैरोलिना
$1,00,000 – $1,15,000 / वर्ष
हाइब्रिडपूर्णकालिकवरिष्ठआवश्यक भाषा: अंग्रेज़ीनैदानिक अनुसंधान
Google Cloud Platform

विवरण

  • Support clinical trials from start-up through maintenance and closeout
  • Review site monitoring reports for potential non-compliance, monitoring gaps, and sponsor oversight needs
  • Assist with essential document review
  • Conduct centralized reviews of clinical listings, EDC queries, protocol deviations, site metrics, and study dashboards
  • Help the Clinical Project Manager evaluate CRO monitor performance
  • Oversee site compliance, quality measures, scope, deliverables, and timelines
  • Maintain study tracking spreadsheets and databases
  • Manage the Trial Master File and verify required documents in investigator files
  • Engage sites proactively to support enrollment and milestone adherence
  • Manage assigned sites independently across compliance, deliverables, relationships, and issue resolution
  • Attend kick-off, investigator, monitor, and other trial meetings
  • Track study timelines and performance metrics while supporting issue resolution
  • Review informed consents, case report forms, study operations manuals, monitoring tools, and related materials
  • Monitor site progress toward data collection, source document verification, and query resolution targets
  • Ensure assigned sites submit safety reports on time
  • Contribute to clinical data listings reviews

आवश्यकताएँ

  • Degree in life science, an advanced scientific or clinical field, or equivalent education and experience
  • At least three years of clinical trial monitoring experience
  • Working knowledge of ICH GCP and applicable regional regulations, including FDA, EMEA, and PMDA requirements
  • Ability to work with limited supervision
  • Excellent written and verbal communication skills
  • Strong attention to detail and problem-solving ability
  • Adaptability when priorities change while maintaining quality
  • Self-directed approach to prioritizing and completing tasks and special projects
  • Ability to handle confidential information with integrity and discretion
  • Effectiveness working across functions and organizational levels
  • Willingness to travel domestically and internationally as needed
  • Proficiency with Microsoft Office, including Excel, Word, Outlook, and PowerPoint

लाभ

  • Hybrid work arrangement
  • Limited domestic and international travel for investigator meetings, site engagement, and oversight activities
  • Equal opportunity employment commitment
  • Support for a diverse workforce

संबंधित नौकरियाँ

Verily

Senior Biostatistician – Clinical Research

Verily
1,001 – 5,000 कर्मचारी
H1B वीज़ा प्रायोजककृत्रिम बुद्धिमत्तापरामर्शस्वास्थ्य सेवा
USसंयुक्त राज्यCAकैलिफ़ोर्नियाMAमैसाचुसेट्सNCउत्तरी कैरोलिनाTXटेक्सास
$1,30,000 – $1,96,000 / वर्ष
हाइब्रिडपूर्णकालिकवरिष्ठआवश्यक भाषा: अंग्रेज़ीनैदानिक अनुसंधान
Python

Lead statistical study design and analysis for Verily’s AI-enabled precision health products. Generate clinical and real-world evidence throughout the product lifecycle.

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