Clinical Research Associate

il y a 2 semaines

Nice, Provence-Alpes-Côte d'Azur, France Pharmiweb Temps plein

About the Role:

A highly motivated Clinical Research Associate with a passion for site management and data integrity will be responsible for overseeing investigator sites, conducting site visits, and developing effective relationships with site staff.

Key Responsibilities:

  • Full ownership of investigator sites, ensuring seamless study execution and compliance.
  • Planning and conducting site visits to monitor study progress and provide guidance to site staff.
  • Developing and maintaining effective relationships with site staff, fostering a collaborative environment and ensuring successful study outcomes.
  • Ensuring the integrity of clinical data, identifying and addressing any discrepancies or issues.

Requirements:

  • 3+ years of CRA experience in the pharmaceutical industry or CRO, with a strong background in site management and data integrity.
  • Excellent organizational skills, with the ability to prioritize tasks and manage multiple projects simultaneously.
  • Able to work in a dynamic environment, adapting to changing priorities and deadlines.
  • Strong IT skills, with proficiency in clinical trial management systems and data management tools.
  • Strong communication skills, with the ability to effectively collaborate with site staff, study teams, and other stakeholders.
  • Fluency in English, with professional proficiency in French.

About Pharmiweb:

Our Clinical Operations team is a supportive and dynamic environment, where you will have the opportunity to develop personally and professionally, working closely with a global study team to solve problems and achieve goals.

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