Remote Study Physician - Clinical Trial Medical Lead

Talanto

Österreich

Remote

EUR 53.000 - 81.000

Vollzeit

vor 45 Stunden
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

Mach aus dieser Rolle ein Vorstellungsgespräch — ein Lebenslauf und ein Anschreiben, die darauf ausgerichtet sind, was dieser Arbeitgeber sucht.

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Benefits dieser Stelle

Medical care plan
Life Assurance
Pension plan
Excellent training

Zusammenfassung

FSP is seeking an experienced Study Physician to join our team in Austria with remote work options. You will be medically responsible across all trial phases and provide specialist oversight from design to reporting.

The role requires MD and at least 4 years of clinical practice, with desirable pharma/CRO exposure and ICH-GCP knowledge. We offer premium salary, health plan, pension, and strong teamwork culture.

Qualifikationen

  • MD physician with minimum 4 years of active clinical practice.
  • Specialization in Pulmonology, Immunology, Internal Medicine, Infectious Diseases, Family Medicine, Pediatrics, Rheumatology, or Emergency Medicine is desirable.
  • Experience in pharma/CRO medical functions or project management is advantageous.
  • Understanding of ICH-GCP regulations and guidelines.
  • Experience as a medical monitor is preferred.
  • Familiarity with data visualization systems and IT platforms.

Aufgaben

  • Medically responsible at the trial level from preparation to reporting.
  • Provide medical oversight from Trial Design Outline to the Clinical Trial Report.
  • Co-author Clinical Quality Monitoring plans and oversee data review.
  • Maintain high medical quality and manage trial-related risks.

Kenntnisse

MD
Clinical practice
Medical monitor
ICH-GCP knowledge
Pharma/CRO exp
Data visualization
Clinical development

Ausbildung

MD degree

Tools

Data visualization tools
IT systems

Jobbeschreibung

FSP is seeking an experienced Study Physician to join our team in Austria with remote work options. You will be medically responsible across all trial phases and provide specialist oversight from design to reporting.

The role requires MD and at least 4 years of clinical practice, with desirable pharma/CRO exposure and ICH-GCP knowledge. We offer premium salary, health plan, pension, and strong teamwork culture.

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