Senior Clinical Research Associate

hace 3 semanas

Madrid, Madrid, España Iqvia Argentina A tiempo completo

Job Summary

Iqvia Argentina is seeking a highly skilled Senior Clinical Research Associate to join our team. As a key member of our clinical research team, you will be responsible for managing clinical trials from site selection to close-out.

Key Responsibilities

  • Perform site selection, initiation, monitoring, and close-out visits to ensure compliance with regulatory requirements and Good Clinical Practice (GCP) guidelines.
  • Develop and implement subject recruitment plans to meet study timelines and enrollment targets.
  • Evaluate the quality and integrity of site practices, including the management of case report forms (CRFs) and data queries.
  • Collaborate with study site staff and client representatives to ensure seamless trial execution.
  • Manage trial progress by tracking regulatory submissions, recruitment, and data query resolution.

Requirements

  • University degree in a scientific discipline or healthcare.
  • At least 2 years of on-site monitoring experience.
  • Good knowledge of clinical research regulatory requirements.
  • Excellent computer skills, including MS Office.
  • Very good command of Spanish and English language.
  • Organizational, time management, and problem-solving skills.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.

What We Offer

  • Resources to promote career growth and development.
  • Leaders who support flexible work schedules and work-life balance.
  • Programs to help build therapeutic knowledge and expertise.
  • Excellent working environment in a stable, international, and reputable company.
  • Attractive benefits package, including company car and mobile phone.

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