Clinical Research Associate



Responsibilities

  • Implement, follow and monitor the clinical trials in France
  • Participate to investigational site selection and site contract negotiation
  • Support the Clinical Project Manager in international coordination of clinical trials and IRB submissions
  • Participate to the writing and preparation of the essential document templates
  • Ensure that study documentation is completed and properly maintained in accordance with all applicable regulations
  • Monitor Investigational Medicinal Products (shipment, accountability, return and documentation)
  • Prepare and submit appropriate site visit reports within timelines
  • Provide regular study updates to AB Science management and update tracking tools

 

Requirements

  • BS, BSN or RN
  • Qualified CRA with 2 to 5 years of field monitoring experience in phase 2 and 3 studies
  • Oncology monitoring experience is a plus
  • Strong knowledge of regulatory environment
  • Computer proficient with the Microsoft Office suite of tools
  • Fluent in English

 

Additional informations

  • Permanent position, available immediately
  • Based in Paris
  • Salary & package to define according skills and experience