Vacatures 121 tot 125 van 127 (ontdubbeld 125)
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Medior Analist Sancties SIM Business Clients
Yacht - Utrecht
Management (SIM). Je start binnen één van de procesdomeinen van DFC: New Client Take On (NCTO) of Client Review (CR), waarbij je periodiek reviews en Event Driven Reviews uitvoert. Binnen SIM ben je een onderdeel van een team- Volledige vacature bekijken
Open sollicitatie Medior CDD Analist
Yacht - Amsterdam
particulieren en zakelijke relaties, denk aan Periodic Reviews (PR) en Event Driven Reviews (EDR). Tot slot heb je aantoonbare ervaring in het identificeren van risico-indicatoren en heb je ervaring met hoog risico dossiers, PEP/Sanctie- Volledige vacature bekijken
Senior Medical Writer remote Life Sciences
Yacht via Talent - Utrecht
clinical regulatory documents and incorporates multiple reviews into successive drafts. Provides QC support for clinical regulatory documents as required (cross-checking data and verifying content from source documents). Reviews Freelance Principal Medical Writer remote Life Sciences
Yacht via Talent - Amsterdam
process of critical review of clinical regulatory documents and incorporates multiple reviews into successive drafts. Provides QC support for clinical regulatory documents as required (cross-checking data and verifying content fromSenior Medical Writer remote Life Sciences
Yacht via Talent - Utrecht
clinical regulatory documents and incorporates multiple reviews into successive drafts. Provides QC support for clinical regulatory documents as required (cross-checking data and verifying content from source documents). Reviews Senior Medical Writer remote Life Sciences
Yacht via Talent - Utrecht
documents and incorporates multiple reviews into successive drafts Provides QC support for clinical regulatory documents as required (cross-checking data and verifying content from source documents) Reviews case report formsSenior Medical Writer remote Life Sciences
Yacht via Talent - Utrecht
documents and incorporates multiple reviews into successive drafts Provides QC support for clinical regulatory documents as required (cross-checking data and verifying content from source documents) Reviews case report formsEr zijn 2 vergelijkbare resultaten weggelaten bekijk ongefilterd