Consultant Clinical Regulatory Affairs & Study Start-Up
- Verfügbarkeit einsehen
- 0 Referenzen
- 85€/Stunde
- 55270 Engelstadt
- auf Anfrage
- de | pl | en
- 15.07.2021
Kurzvorstellung
Over 17 years experience in Regulatory Affairs and Study Start-Up in the Clinical Trials environment.
Regulatory Project Lead in local, European and global phase I-IV CNS, oncology, dermatology, respiratory diseases, in adult and pediatric studies.
Regulatory Project Lead in local, European and global phase I-IV CNS, oncology, dermatology, respiratory diseases, in adult and pediatric studies.
Qualifikationen
Ausbildung
Regulatory Affairs Associate
Ausbildung
2006
Wiesbaden
Wiesbaden
Slawische Philologie, Jura, BWL
n.v.
2004
Mainz
Mainz
Über mich
Over 17 years experience in Regulatory Affairs and Study Start-Up in the Clinical Trials environment.
Regulatory Project Lead in local, European and global phase I-IV CNS, oncology, dermatology, respiratory diseases in adult and pediatric studies.
Vast knowledge in clinical trial submissions and life-cycle in Europe (espacially DACH-region and Poland).
Speaking German, English and Polish fluently.
Looking for freelance opportunity in the clinical trials environment in Rhine-Main region or remotely.
Regulatory Project Lead in local, European and global phase I-IV CNS, oncology, dermatology, respiratory diseases in adult and pediatric studies.
Vast knowledge in clinical trial submissions and life-cycle in Europe (espacially DACH-region and Poland).
Speaking German, English and Polish fluently.
Looking for freelance opportunity in the clinical trials environment in Rhine-Main region or remotely.
Persönliche Daten
Sprache
- Deutsch (Muttersprache)
- Englisch (Fließend)
- Polnisch (Muttersprache)
Reisebereitschaft
auf Anfrage
Arbeitserlaubnis
- Europäische Union
Home-Office
bevorzugt
Profilaufrufe
470
Alter
50
Berufserfahrung
20 Jahre und 10 Monate
(seit 01/2004)
Projektleitung
10 Jahre
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