Site Manager (m/w) Clinical Operations

Beschreibung

Tätigkeitenbeschreibung
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Site Manager (m/w) Clinical Operations

Aufgaben:
serve as a primary contact point between the sponsor and the investigational site for the conduct of early development and/or clinical pharmacology studies

Qualifikation:
- 4-year University degree in Life Sciences, Nursing, or related scientific field is required
- Experience in monitoring ED&CP studies is preferred
- A minimum of 1 year of clinical trial monitoring experience is preferred,
- Good working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines.
- Good IT skills in appropriate software and company systems
- willingness to travel with occasional/regular overnight stay
- proficient in speaking and writing German and English.

Projektstart:
- 18.05.2015

Dauer:
- 22.05.2016 (100%, fulltime), 50% Reisezeit

Ort:
- deutschlandweit

Bei Interesse senden Sie uns bitte Ihr Profil als Word-Datei und Ihren Stundensatz (exkl. aller Nebenkosten) an

Wir melden uns dann in Kürze bei Ihnen zurück.

Vielen Dank!

Fähigkeiten (Must have)
GCP, ISO, SOP