[Emploi] Medical Coordinator at AlzProtect

Mise en ligne le 17 décembre 2018

Location : Loos (Lille) – Parc Eurasanté

AlzProtect is a biopharmaceutical company engaged in the discovery and development of therapeutic solutions in the field of neurodegenerative diseases

Within the Clinical Development Department, you make an important contribution to our drug development programs and work closely with those responsible for medicinal chemistry, pharmacology and pharmaceutical development. Your enthusiasm, your creativity and your taste for innovation will be assets within Alzprotect


  • Contribute to the selection of CROs and external vendors to  conduct and plan assigned clinical studies
  • Discuss and manage study plans, timelines & budget with selected CRO and external vendors, from initial planning until final reporting phase
  • Ensure close interaction with functional experts and key opinion leaders involved in the clinical study by acting as single point of contact for assigned clinical studies
  • Act as clinical study representative in clinical project sub teams and/or development project teams
  • You coordinate national or international clinical trials in relation with the internal team and the providers involved
  • You ensure the implementation and monitoring coordination of clinical trials: Documentation, investigative relationships, regulatory and budgetary aspects
  • You coordinate the stakeholders involved in clinical trials
  • You implement and monitor actions to meet recruitment deadlines and good clinical practices.


  • Ideally medical training or at least scientific Master degree, you justify an experience of at least 2 years in the management of clinical trials
  • Ideally, experience in clinical phase 1 and/or 2 (proof of concept)
  • Experience in outsourcing management (CROs) is a plus
  • Experience in "orphan drug" is a plus
  • Experience in Neurology and more particularly in the field of neurodegenerative diseases is a plus
  • English and French fluent (oral and written)
  • Mastery of good clinical practices and adherence to the principles of quality assurance
  • Sense of service and communication
  • Analytical skills, synthesis skills, open-mindedness
  • Autonomy, rigor, method and organization



  • Send your CV and motivation letter by E-mail to Nathalie Faltraue: