CSL
CSL
CSL og‘ir va kam uchraydigan kasalliklar bilan yashayotgan insonlar uchun bioterapevtik preparatlar va vaksinalar ishlab chiqadigan global biotexnologiya va sog‘liqni saqlash kompaniyasidir. Uning faoliyatiga immunitet tanqisligi, irsiy qon ketish buzilishlari va Alfa-1 antitripsin yetishmovchiligini davolash usullarini taqdim etuvchi CSL Behring; grippga qarshi vaksinalarning yirik yetkazib beruvchisi CSL Seqirus; temir tanqisligi va nefrologiyaga yo‘naltirilgan CSL Vifor kiradi. Keng qamrovli tadqiqot va ishlanmalar tarmog‘i ko‘magida CSL plazmani fraksiyalash, rekombinant oqsil texnologiyasi, hujayra va gen terapiyasi, shuningdek vaksinalar yo‘nalishlarida faoliyat yuritadi. Bosh qarorgohi Avstraliyaning Melburn shahrida joylashgan kompaniya 100 dan ortiq mamlakatdagi bemorlarga xizmat ko‘rsatadi hamda tadqiqot, ishlab chiqarish, sog‘liqni saqlash va biotexnologiya sohalarida karyera imkoniyatlarini taklif qiladi.

Principal Clinical Scientist, Hematology Clinical Development - Onsite

Lead scientific contributions to CSL’s hematology clinical development programs. Support study execution, clinical data interpretation, regulatory documentation, medical monitoring, and external oversight committees.

Tavsif

  • Support scientific planning for hematology clinical development programs and individual studies
  • Provide clinical development expertise to help deliver assigned programs safely, efficiently, on schedule, to high quality, and in compliance with requirements
  • Develop and review program and study documents and training materials, including clinical development plans, investigator brochures, protocols, eCRFs, ICFs, study reference manuals, and investigator training
  • Help design and execute medical monitoring strategies that protect patient safety and data integrity, including ongoing blinded-data review
  • May lead the development of a Clinical Development Program
  • Help prepare and review manuscripts, conference abstracts, and related scientific materials
  • Work with internal and external cross-functional partners to convert clinical strategy and protocols into operational deliverables
  • Analyze and interpret clinical data
  • Prepare clinical study reports, scientific meeting presentations, peer-reviewed publications, and regulatory submission materials
  • Coordinate processes and relationships supporting external study oversight committees, including steering, independent data monitoring, and adjudication committees

Talablar

  • PhD, master’s degree, or bachelor’s degree in a science-related discipline
  • An advanced degree such as an MSc or PhD in a science-related discipline is preferred
  • PMP certification is preferred
  • PhD holders need at least 4 years of experience in one or more biotechnology or pharmaceutical R&D functions
  • MS holders need at least 6 years of experience in one or more biotechnology or pharmaceutical R&D functions
  • BS holders need at least 8 years of experience in one or more biotechnology or pharmaceutical R&D functions
  • At least 3 years of clinical research experience
  • Deep knowledge of pharmaceutical drug development and manufacturing processes spanning CMC, non-clinical, clinical, and Regulatory Affairs activities
  • Ability to collaborate across functions in a matrix organization
  • Strong written and verbal communication skills
  • High attention to detail in processes, communications, and documentation
  • Demonstrated ability to work independently and collaboratively
  • Creative problem-solving ability
  • Experience overseeing CROs

Imtiyozlar

  • CSL benefits are available; consult “How CSL Supports Your Well-being” for details

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