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Open nowFirst seen 3 hours ago

Freelance of vast - Clinical Research Associate voor medische hulpmiddelen - Diegem

EngiFlex117 open roles

Where
Diegem, Belgium
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Your applicationOpen nowFreelance of vast - Clinical Research Associate voor medische hulpmiddelen - DiegemEngiFlex · Diegem, Belgium

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The clock on this job

Early applications get read.

13.7% of postings close within 7 days. Measured by our own scanner across the market. EngiFlex postings stay open a median of 6 days.

Share of postings closed within
  1. 2.3%1 day
  2. 4.8%3 days
  3. 13.7%7 days
  4. 22.1%14 days
  5. 37.6%30 days
  6. 59.1%60 days
This job: first seen 3 hours ago

EngiFlex median: 6 days open

The posting

Functie omschrijving

Jouw baan als Clinical Research Associate

Als Clinical Research Associate begeleid je klinische studies binnen de sector van medische hulpmiddelen. Je ondersteunt studiecentra tijdens het volledige studietraject, van de initiatie tot en met de close-out. Daarbij zie je toe op de datakwaliteit, patiëntveiligheid en naleving van de geldende wet- en regelgeving. Je werkt samen met onderzoekers, klinische teams, leveranciers en andere stakeholders.

De functie omvat een hybride werkmodel vanuit Diegem, gecombineerd met frequente verplaatsingen naar studiecentra in België.

Je verantwoordelijkheden

  • Studiecentra begeleiden vanaf de opstart tot de studieafsluiting.
  • Monitoringbezoeken uitvoeren volgens het protocol en de GCP-richtlijnen.
  • De datakwaliteit en patiëntveiligheid tijdens klinische studies bewaken.
  • Studiecentra ondersteunen bij operationele vragen en documentatie.
  • De rekrutering, retentie en voortgang van studies actief opvolgen.
  • Samenwerken met onderzoekers, leveranciers en interne projectteams.
  • Bevindingen rapporteren en corrigerende acties opvolgen.

📝 Jouw profiel

Je werkt gestructureerd, communiceert duidelijk met verschillende stakeholders en behoudt het overzicht wanneer meerdere studies gelijktijdig lopen. Je neemt proactief verantwoordelijkheid op en weet de juiste prioriteiten te stellen.

Hard skills

  • Een bachelor in Life Sciences, Biomedische Wetenschappen, Verpleegkunde of een gelijkwaardige opleiding.
  • Minstens 2 jaar ervaring binnen klinisch onderzoek.
  • Ervaring met medical device monitoring.
  • Goede kennis van GCP-richtlijnen en klinische regelgeving.
  • Een vlotte kennis van het Nederlands en Engels. Frans is een pluspunt.

💼 Aanbod

Je zal deel uitmaken van een groeiende KMO met ruimte voor initiatief en persoonlijke ontwikkeling. Wij zorgen ervoor dat je in een uitdagende maar aangename werkomgeving terecht komt met leuke collega's. Samen met jou stippelen we een carriereplan uit, met aandacht en budget voor bijkomende opleidingingen / certificaties. Je kan rekenen op een motiverend salaris, aangevuld met extralegale voordelen, inclusief bedrijfswagen (of alternatieve vergoeding). (Freelance is ook mogelijk)

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