Zurück zur Suche.NonStop Recruitment CZ - Submission Specialist - Germany
| Beschäftigungstyp: | Permanent |
| Standort: | Germany |
| Gehalt: | 40000 |
| Sprachen: | Englisch, Deutsch |
Details für die Anzeigenschaltung
- Name:NonStop Recruitment CZ
- Veröffentlichung:03-02-2012
- Code:MS/53006/31
Submission Specialist - Germany
A new job opportunity has arisen with one of the leading, international CROs with their offices in Southern Germany. The Clical Research department is searching for an experienced Submission Specialist with an experience in submissions to the German ethics commission. This role will be based in Bavaria or home based anywhere in Germany.
As a Submission Specialist you will be responsible for creating start up documents in Germany, Switzerland and Austria. You will be the key person for collecting and reviewing regulatory documents for the submission of the German ethics commission and other German regulators. This challenging role also includes the responsibility for creating and amending deficiency letter and preparation of application form.
The suitable candidate will have a good working experience within the pharmaceutical/CRO business combined with in-depth knowledge of the mentioned above. You will ideally have some experience in negotiating the investigator contracts as well as budget. This role requires fluency in both German and English languages and excellent attention to detail as well as outstanding communication skills.
A new job opportunity has arisen with one of the leading, international CROs with their offices in Southern Germany. The Clical Research department is searching for an experienced Submission Specialist with an experience in submissions to the German ethics commission. This role will be based in Bavaria or home based anywhere in Germany.
As a Submission Specialist you will be responsible for creating start up documents in Germany, Switzerland and Austria. You will be the key person for collecting and reviewing regulatory documents for the submission of the German ethics commission and other German regulators. This challenging role also includes the responsibility for creating and amending deficiency letter and preparation of application form.
The suitable candidate will have a good working experience within the pharmaceutical/CRO business combined with in-depth knowledge of the mentioned above. You will ideally have some experience in negotiating the investigator contracts as well as budget. This role requires fluency in both German and English languages and excellent attention to detail as well as outstanding communication skills.
Due to the nature of this position, the recruiter has requested to restrict applications by location. Only candidates in Europe (EEA) may apply.
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