CTI Clinical Trial and Consulting Services
CTI Clinical Trial and Consulting Services
CTI Clinical Trial and Consulting Services एक कॉन्ट्रैक्ट रिसर्च ऑर्गनाइज़ेशन है, जो क्लिनिकल विकास की पूरी प्रक्रिया में जैव-प्रौद्योगिकी और फार्मास्यूटिकल प्रायोजकों को सेवाएँ प्रदान करता है। इसका कार्य फेज़ I–IV अध्ययनों में क्लिनिकल ट्रायल संचालन, नियामकीय रणनीति, प्रयोगशाला और बायोएनालिटिकल सेवाओं, वास्तविक-विश्व साक्ष्य तथा अनुसंधान केंद्र प्रबंधन तक फैला हुआ है। CTI को दुर्लभ रोगों, कोशिका और जीन थेरेपी, ऑन्कोलॉजी, न्यूरोलॉजी तथा प्रत्यारोपण जैसे क्षेत्रों में अनुभव है। यह अध्ययन डिज़ाइन, साइट प्रबंधन, रोगी भर्ती, निगरानी, सुरक्षा और फार्माकोविजिलेंस, बायोमेट्रिक्स तथा गुणवत्ता आश्वासन में सहायता करता है। कंपनी एकीकृत ट्रायल सेवाओं को रोगी-केंद्रित अनुसंधान और वैश्विक नियामकीय मार्गदर्शन के साथ जोड़ती है।

Site Contract Specialist – Remote in Poland

Remote, full-time role in Poland supporting confidentiality and clinical trial agreements for CTI Clinical Trial and Consulting Services. The position coordinates contract negotiations, execution, tracking, and regulatory file management.

विवरण

  • Contact study sites and follow up as needed to convert confidentiality agreement (CDA) and clinical trial agreement (CTA) drafts
  • Manage contract language within approved sponsor guidelines and collaborate with legal counsel on revisions and negotiations
  • Coordinate the completion and execution of CDAs and CTAs
  • Participate in internal and external project meetings and provide updates on CDA and CTA progress
  • Maintain contract files and internal and external CDA and CTA tracking records
  • Update CTA status in the internal study start-up module for assigned studies
  • Support contract preparation, review, revision, execution, and filing
  • Inform relevant stakeholders about key terms, including expiration dates, renewal provisions, and compliance obligations
  • Support CDA preparation, review, negotiation, execution, and filing
  • Maintain CDA tracking records and archives
  • Process new consultant documentation and maintain related files

आवश्यकताएँ

  • Paralegal certification or an associate degree
  • At least two years of experience in a professional administrative or business role
  • Experience with a pharmaceutical company or Clinical Research Organization (CRO) preferred
  • Basic knowledge of medical and pharmaceutical terminology preferred

लाभ

  • Structured mentoring and leadership development courses
  • Tuition reimbursement
  • Dedicated training department
  • Comprehensive health benefits
  • Vacation packages
  • Hybrid work-from-home opportunities
  • Paid parental leave
  • CTI Cares program
  • Support for work-life balance

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