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Site Management Professional

1 tydzień temu

Warszawa, Mazovia, Polska IQVIA Argentina Pełny etat

IQVIA Argentina Job Description

We are seeking a highly experienced Clinical Research Associate to join our dynamic team.

The selected candidate will be responsible for conducting site visits, providing support in the development of recruitment plans, and ensuring that all documentation is up-to-date.

Main Responsibilities

  • Carry out thorough site assessments to guarantee adherence to regulatory requirements and study protocols
  • Develop and implement strategies to boost subject participation and retention rates
  • Regularly communicate with assigned sites to address questions and concerns
  • Work closely with internal teams to resolve complex study execution challenges
  • Offer expert advice to site personnel on protocol and study processes

Essential Qualifications

  • Bachelor's degree in a healthcare or scientific discipline or equivalent
  • At least 2 years of experience in clinical trial monitoring (ideally in CVRM/Oncology)
  • Strong written and verbal communication skills, including proficiency in Polish and English