CTI Clinical Trial and Consulting Services
CTI Clinical Trial and Consulting Services
CTI Clinical Trial and Consulting Services klinik rivojlanish jarayonining barcha bosqichlarida biotexnologiya va farmatsevtika homiylariga xizmat ko‘rsatuvchi shartnoma asosidagi tadqiqot tashkilotidir. Kompaniya faoliyati I–IV fazadagi tadqiqotlar doirasida klinik sinovlarni o‘tkazish, tartibga solish strategiyasi, laboratoriya va bioanalitik xizmatlar, real hayot ma’lumotlari hamda tadqiqot markazlarini boshqarishni qamrab oladi. CTI kam uchraydigan kasalliklar, hujayra va gen terapiyasi, onkologiya, nevrologiya hamda transplantatsiya kabi yo‘nalishlarda tajribaga ega. Kompaniya tadqiqot dizayni, markazlarni boshqarish, bemorlarni jalb qilish, monitoring, xavfsizlik va farmakologik nazorat, biometrika hamda sifatni ta’minlash jarayonlarini qo‘llab-quvvatlaydi. CTI kompleks tadqiqot xizmatlarini bemorga yo‘naltirilgan tadqiqotlar va global tartibga solish bo‘yicha yo‘l-yo‘riq bilan birlashtiradi.

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.

Tavsif

  • 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

Talablar

  • 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

Imtiyozlar

  • 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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