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LabConnect
LabConnect
501 – 1,000 कर्मचारी
औषधियाँजैव प्रौद्योगिकीस्वास्थ्य सेवा

LabConnect एक वैश्विक केंद्रीय प्रयोगशाला समाधान भागीदार के रूप में क्लिनिकल परीक्षणों और दवा विकास में सहायता करता है। कंपनी केंद्रीय और विशेषीकृत जैव-विश्लेषणात्मक परीक्षणों को रेडियोफार्मास्यूटिकल सेवाओं, विकेंद्रीकृत और घर के निकट नमूना संग्रह, कस्टम संग्रह किट, सहवर्ती निदान, परीक्षण सत्यापन और प्रयोगशाला डेटा प्रबंधन के साथ जोड़ती है।

इसकी टीमें प्रायोजकों और कॉन्ट्रैक्ट रिसर्च संगठनों को ऑन्कोलॉजी, टीकों तथा कोशिका और जीन थेरेपी सहित विभिन्न क्षेत्रों में जटिल अनुसंधान कार्यक्रमों का समन्वय करने में सहायता करती हैं। LabConnect डेटा सामंजस्य, नियामक और वैज्ञानिक परियोजना प्रबंधन तथा वाणिज्यिक और बाजार-पश्चात सहायता भी प्रदान करता है। इसका जोर क्लिनिकल अनुसंधान जीवनचक्र के दौरान प्रयोगशाला संचालन को विश्वसनीय क्रियान्वयन में बदलने पर है।

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कंपनी की नौकरियाँ

Associate Data Manager, Clinical Laboratory Data

Reconcile and validate laboratory data streams at LabConnect, supporting compliant clinical trial transfers. Review data specifications, resolve client queries, and coordinate corrections with internal teams.

USसंयुक्त राज्यTNटेनेसीरिमोटपूर्णकालिकजूनियरमध्य स्तरडिग्री आवश्यक नहींआवश्यक भाषा: अंग्रेज़ीडेटा वैज्ञानिक
Google Cloud Platform

विवरण

  • Reconcile and validate regulated laboratory data streams for clients
  • Correct missing, inconsistent, or inaccurate data
  • Review laboratory files against transfer specifications
  • Prepare test laboratory data for transfer files
  • Develop simple study transfer specifications and notify clients of changes
  • Help improve real-time validity checks in LabConnect’s central laboratory information management system
  • Maintain transfer specifications under the study Data Manager’s direction
  • Design systems that support project needs
  • Send scheduled or requested data transfers to clients and designated recipients
  • Check transmissions against required file structure, format, layout, and specifications
  • Keep analyte reference ranges, decimal precision, units, and correlation factors consistent
  • Create, install, and verify laboratory unit conversion tables
  • Answer client questions about clinical data streams and record outcomes in client databases
  • Work with internal teams and Investigator Support Services to resolve queries and correct errors
  • Keep study schedules aligned with contracts and client communications
  • Complete routine work under the group manager’s direction

आवश्यकताएँ

  • An associate degree or university program certificate in a biological science is preferred
  • Four to six years of clinical trial industry experience is strongly preferred
  • A comparable combination of education and experience may be considered
  • Laboratory experience is preferred
  • Experience with clinical trial protocol development and FDA 21 CFR Part 11/GCP is strongly preferred
  • ASCP Medical Technologist or Medical Laboratory Technician certification is preferred
  • Strong attention to detail
  • Ability to follow established timelines, processes, and procedures
  • Strong planning and problem-solving abilities
  • Ability to work independently and collaboratively
  • Organization, time management, communication, multitasking, interpersonal, and listening skills
  • Ability to adapt to changing environments and requirements
  • Verbal comprehension and ability to convey client needs to team members
  • Ability to make timely, considered decisions
  • Customer service and client relationship management skills
  • Ability to sit at a desk and work on a computer for extended periods
  • Ability to communicate effectively by phone, video, and email
  • Ability to use hands and fingers to operate a computer and other office equipment

लाभ

  • Equal opportunity employer committed to diversity and an inclusive workplace
  • Reasonable accommodations may be made for individuals with disabilities to perform essential job functions
  • Minimal travel required

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