ERGOMED
ERGOMED
1 001 – 5 000 Xodimlar
KonsaltingLogistikaSog‘liqni saqlash
ERGOMED biotexnologiya va farmatsevtika kompaniyalarini dori vositalarini ishlab chiqish jarayonining barcha bosqichlarida qo‘llab-quvvatlaydigan global sog‘liqni saqlash xizmatlari guruhidir. Uning tarkibiga Ergomed Clinical Research, PrimeVigilance va ADAMAS Consulting kiradi. Guruh klinik tadqiqotlar tashkiloti xizmatlari, farmakovigilans va tibbiy axborot ko‘magi, shuningdek, GxP auditini taqdim etadi. Kompaniya onkologiya, kam uchraydigan kasalliklar va boshqa murakkab klinik tadqiqotlar ustida ishlaydi, uning faoliyati qariyb 100 mamlakatni qamrab oladi.

Pharmacovigilance Auditor (Freelance) – Remote in Spain

Freelance Pharmacovigilance Auditor responsible for GVP audits and quality assurance projects for pharmaceutical and biotechnology clients. Remote in Spain with travel of up to 40%.

Tavsif

  • Plan, prepare, conduct, document, and follow up on a range of pharmacovigilance audits
  • Create and monitor CAPA plans through completion
  • Conduct audits using detailed knowledge of regulatory requirements and Good Pharmacovigilance Practice (GVP)
  • Deliver GVP quality assurance projects for pharmaceutical and biotechnology clients

Talablar

  • Experience leading and conducting internal and external pharmacovigilance audits for diverse stakeholders
  • Expertise in national and international pharmacovigilance legislation and guidelines
  • Strong project management skills, with a record of delivering work on schedule
  • Practical problem-solving ability, including identifying issues and recommending solutions
  • A bachelor’s degree in life sciences is preferred
  • Willingness to travel up to 40%
  • Capability to conduct audits remotely

Imtiyozlar

  • Freelance engagement available at full-time 1.0 FTE or part-time 0.6+ FTE
  • Work remotely from Spain
  • Conduct audits remotely
  • Travel of up to 40%
  • Supportive and collaborative working environment
  • Encouragement for ongoing professional development
  • Opportunity to contribute across the pharmaceutical and biotechnology sectors
  • Work alongside experts in clinical research, pharmacovigilance, and quality consulting

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