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responsible for trial master files or relevant mirror files
- responsible for all in-house filing of different studies
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responsible for all study related correspondence to/from sites, to/from sponsor, to/from subvendors, transmittal of DCF, CRF, Reg Docs, ....
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carry out study related (back)translations
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responsible for long-term storage according to the SOPs (both in-house and of the different sponsors)</il>
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complete and organize all study documents at time of audit
- study setup and close out
- compose binders
- organize with subvendors
- assure green light to start up study
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understand the EC/CA submission process in Belgium, The Netherlands and France
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serve as backup of CRC in case of absence due to on-site visits, holidays, sickness leave, ...
- maintain a close and professional intraction with the different investigational sites
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minimum 2 year of experience in a administrative function
- excellent in social and interpersonal contacts
- able to handle multiple tasks to meet deadlines
- customer-oriented, enthousiastic, dynamic
- excellent in Dutch, French and English (oral as well as written)
- experience in Microsoft Office
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(medical) managing assistant or equivalent by experience
- minimum 2 year experience in a similar function
KasaConsult offers you a challenging job with an interesting salary and extralegal benefits within a pleasant work atmosphere and on a location without traffic jams.
Possibility of development of your personal skills via courses.
Please send your reaction preferably by e-mail to k.seldeslagh(at)kasaconsult.com
