PSI CRO AG
PSI CRO AG
1 001 – 5 000 Xodimlar
KonsaltingLogistikaSog‘liqni saqlash
PSI CRO AG klinik tadqiqotlarni qo‘llab-quvvatlaydigan va asosiy ahamiyatga ega 2- hamda 3-bosqich tadqiqotlariga e’tibor qaratadigan global shartnoma asosidagi tadqiqot tashkilotidir. Kompaniya faoliyati ichakning yallig‘lanish kasalliklari, onkologiya, gematologiya, yuqumli kasalliklar, ko‘p skleroz va kam uchraydigan kasalliklarni o‘z ichiga olgan turli terapevtik yo‘nalishlarni qamrab oladi. PSI CRO AG klinik tadqiqotlarni rejalashtirish va moliyaviy kuzatish uchun o‘zining maxsus platformasidan foydalanib, jamoalarga tadqiqot muddatlari va budjetlarini nazorat qilishda yordam beradi. Kompaniya profili sog‘liqni saqlash va konsalting sohalaridagi tajribani sifat, muvofiqlik va tadqiqotlarni ishonchli tarzda o‘tkazishga e’tibor bilan birlashtiradi.

Clinical Research Associate II in Australia

Lead clinical trial monitoring and site management across Australia, supporting study start-up, regulatory submissions, data quality, and patient safety for PSI CRO AG.

Tavsif

  • Conduct and document onsite monitoring visits across clinical trials
  • Support study start-up activities
  • Review case report forms, verify source data, and resolve queries
  • Coordinate site budgets and contract negotiations
  • Track study progress at the country level
  • Manage communication and ongoing relationships with clinical sites
  • Coordinate with internal support functions and external vendors
  • Update project teams on study progress and operational matters
  • Contribute to feasibility assessments and research
  • Assist regulatory colleagues with study submission documentation
  • Oversee clinical activities for full-service global projects in Australia
  • Maintain study timelines, targets, and applicable clinical research standards
  • Develop productive relationships with investigators and research sites
  • Protect participant rights, safety, and well-being while maintaining data quality and compliance

Talablar

  • Degree in life sciences, pharmacy, nursing, or a comparable combination of education, training, and experience
  • At least two years of independent onsite monitoring experience in Australia
  • Experience conducting Phase II and/or Phase III monitoring visits
  • Background in inflammatory bowel disease, oncology, or infectious diseases is advantageous
  • Professional working proficiency in English
  • Working knowledge of Microsoft Word, Excel, and PowerPoint
  • Strong planning and multitasking abilities in a dynamic team setting
  • Effective communication, collaboration, and problem-solving skills
  • Willingness and ability to travel

Imtiyozlar

  • Competitive compensation
  • Hybrid schedule with two flexible days and three office days
  • Access to an onsite gym
  • Five additional wellness-leave days
  • Professional development and learning opportunities
  • Opportunity to contribute to the clinical research industry
  • Ongoing support from colleagues worldwide
  • Practical learning through day-to-day work
  • Structured development programs
  • Multiple paths for continued career growth

O‘xshash ish o‘rinlari