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CTI Clinical Trial and Consulting Services
CTI Clinical Trial and Consulting Services
1 001 – 5 000 Xodimlar
BiotexnologiyaKonsaltingSog‘liqni saqlash
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.
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Kompaniyadagi ish o‘rinlari

Senior Clinical Research Associate II – UK Remote

Senior Clinical Research Associate II overseeing UK clinical trial sites for CTI Clinical Trial and Consulting Services. The role includes site visits, remote monitoring, enrollment support, and regulatory compliance.

GBBuyuk BritaniyaMasofaviyTo‘liq stavkaSeniorTalab Qilinadigan Til: inglizchaKlinik tadqiqot
Google Cloud Platform

Tavsif

  • Act as CTI’s primary contact for assigned clinical trial sites
  • Carry out pre-study, site initiation, interim monitoring, and close-out visits
  • Deliver all site visit documentation in line with the Monitoring Plan and required deadlines
  • Support or lead study start-up, feasibility, pre-study, and site selection activities
  • Gather, review, and maintain essential and regulatory documentation
  • Complete required training and attend investigator, client, and project team meetings
  • Develop and execute subject enrollment plans for assigned sites
  • Oversee the storage, dispensing, and accountability of investigational products and trial materials
  • Manage site activities and report site status to the Clinical Project Manager
  • Perform remote monitoring in accordance with the study-specific Monitoring Plan
  • Use systems and reports to monitor subject status, CRF retrieval, source document review, regulatory records, and investigational products
  • Contribute to project-specific work as a member of the Project Team

Talablar

  • Three to five years of clinical research experience as a CRA or in a related profession
  • Background in life sciences
  • Strong knowledge of ICH-GCP and applicable regulatory requirements
  • Ability to conduct pre-study, site initiation, interim monitoring, and close-out visits
  • Ability to complete site visit deliverables within required deadlines
  • Knowledge of applicable regulations, standard operating procedures, and ICH-GCP
  • Ability to support or oversee study start-up, feasibility, pre-study, and site selection activities
  • Ability to collect, review, and track essential and regulatory documents
  • Ability to complete required general and study-specific training
  • Ability to participate in investigator, client, and project team meetings, including presentations
  • Ability to develop and implement subject enrollment strategies
  • Ability to manage investigational products and trial-related materials
  • Ability to conduct site management and remote monitoring activities
  • Ability to use systems and reports to track subject status, CRF retrieval, source document review, regulatory documents, and investigational products

Imtiyozlar

  • Structured mentoring program
  • Leadership development courses
  • Dedicated training department
  • Support for continuing education
  • Hybrid work opportunities
  • CTI Cares community and global giving opportunities
  • Work contributing to the development of life-changing treatments

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