Ervaren CRA oncologie
Deze vacature staat offline! |
| De opdrachtgever
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CRO in de randstad.
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| De omschrijving
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Main tasks:
- to select potential investigators
- verification of the CRF data versus source documents
- control of the site performance based on protocol and GCP guidelines
- to act as an intermediate between sponsor and investigator
- maintenance of contacts woth sites for EC submissions and follow-up
- writing (site) visit reports
- to maintain investigator file, maintain records of status of sites and patients using databases as appropriate.
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| De eisen
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- HBO or acedemic level (para-) medical education
- Knowledge of GCP guidlines
- Knowledge of and experience with medical and/ or oncological clinical research
- Oncology training course (internal or external)
- Adequate knowledge of the verbal and written English and Dutch language.
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| Contactinformatie
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Voor meer informatie over deze functie kunt u zich wenden tot:
Dr. Arjan van den Wijngaard
Consultant Medical
Biltstraat 443
3572 AW Utrecht
tel 030 231 7350
mobiel 06 50650550
Geinteresseerden kunnen hun c.v. rechtstreeks mailen naar info@pharmamediair.nl |
