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CRA

Introduction


You have a medical/science background, are perfect bilingual (ENG + one other EU language, like French, Dutch, German, Italian, Spanish), are flexible to travel through Belgium and Europe ?



Company/Department


Our client is an international company active in the academic research in cancer care.


Function information


The CRA is responsible for “on-site” quality control of clinical trials to ensure that a clinical trial is conducted, recorded and reported in accordance with the protocol, the principles of Good Clinical Practice (GCP) and the applicable regulatory requirements.

Main responsibilities / Major Activities

  • Perform on-site monitoring visits according to the monitoring plan and following the Standard Operating procedures (SOPs) and ICH-GCP guidelines
  • Ensure and control sites’ compliance with study protocol and regulatory obligations
  • Address issues in a manner that is beneficial for the site and the intern team
  • Report the findings of the “on-site” monitoring visits according to intern Standards
  • Follow the sites’ findings until resolution, with the support of the intern study team and Quality Assurance and Control unit
  • Perform site staff training whenever needed during the study conduct
  • Ensure close collaboration between all actors of clinical trial research, as a privilege link between investigational sites and the intern study team.

Requirements


  • University degree or equivalent in Health Sciences
  • Practical knowledge of the conduct of clinical trials
  • Prior experience of at least 2 years as CRA and prior experience in Oncology
  • Ability to travel 50% of working time across European countries
  • Languages: English (written & spoken) is mandatory, and at least one other EU language (French, Dutch, German, Italian, Spanish)
  • Excellent organization
  • Good communication skills
  • Independent and team-player.

Offer


A long term contract full time within a research company in Brussels: junior package with insurances, mealvouchers, transport, laptop and mobile phone.


Information


Sybille Ponet

sybille.ponet@xpepharmascience.com

02/801.16.65


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