Consultant Early Clinical Development Oncology (m/f/n) – Freelance – on hold

  • Position zu besetzen ab 10. Juni 2019
  • Permanent-ID OCR-FL-712
  • Branche Pharma
  • Beschäftigungsform Freelance/ Contracting
  • Standort Deutschland / 6x
  • Kategorien Beschäftigungsform, Branche, Freelance/Contracting, Pharma

Aufgaben
Consultancy in the area of early clinical development in oncology with the aim to ensure data quality for regulatory submission.

• Review of clinical study data, medical monitoring, and update of regulatory documents
• Advice on clinical development programs within clinical oncology
• Review of patient-level clinical study data provided in electronic format, medical monitoring according to Merck processes provided in electronic format, update of regulatory documents provided in electronic format

 

Anforderungen
– Early clinical development Oncology (> 5 years)
– Medical Monitoring (> 5 years)
– Review of clinical study data (> 5 years)
– Review of patient level clinical study data (> 5 years)
– Regulatory submission to FDA/EMA (> 5 years)
– Writing regulatory documentations (> 5 years)
– German and English business fluent

 

Zusätzliche Informationen
Standort: Darmstadt
Projektbeginn: 10.06.2019
Projektlaufzeit: ca. 8,5 Monate
Projektumfang: 720 h
Verfügbarkeit: 2-3 Tage / Woche
Remote Support: tbd

 

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