Job Description

We are seeking an experienced Clinical Research Associate (CRA) to support monitoring and site management activities across multiple studies. The role involves close collaboration with study teams, sites, and cross-functional stakeholders, with a strong commitment to patient safety, data integrity, and product quality.

Key Responsibilities

  • Conduct on-site and remote monitoring activities , including visit preparation, follow-up, site contact, and report writing.
  • Support site start-up activities , including EC/CA submissions, contract negotiation, and essential document collection.
  • Attend study meetings and collaborate with cross-functional teams and sites throughout all study phases.
  • Provide support in audit preparation and responses .
  • Schedule and conduct monitoring visits according to the study monitoring plan.
  • Review informed consents, regulatory files, and site st...

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