Clinical Research Associate

hace 1 mes


Madrid, Madrid, España Pharmiweb A tiempo completo

We are seeking a highly skilled Clinical Research Associate to join our team at ICON. As a Clinical Research Associate, you will be responsible for conducting and completing remote site management activities, maintaining timelines, and ensuring accuracy and completeness of data entered into ICON systems.

Key Responsibilities:

  • Become familiar with ICON's SOPs/WPs, ICH GCP guidelines, appropriate regulations, ICON systems, and the principles of and assist with investigator recruitment
  • Maintain timelines and ensure accuracy and completeness of data entered into ICON systems
  • Serve as the primary in-house contact for sites and investigators participating in studies
  • Conduct and complete remote site management activities, with support as needed, according to applicable SOPs and the Study Monitoring Plan
  • Contact Clinical sites for specific requests (e.g., enrolment updates, missing documentation, data entry timeliness, data query follow-up, CDA finding follow-up, and action Item resolution or other sponsor-specific CRA tasks)

Requirements:

  • Minimum Bachelor's degree in a life science
  • At least 12 months of a CTA/Clinical Trial Assistant or similar role experience within the clinical/pharmaceutical industry
  • Understanding of ICH GCP Compliance
  • Excellent communication and organizational skills
  • Able to travel as needed (drive and fly)
  • Maintain Sponsor and patient confidentiality

What We Offer:

We offer a competitive salary package, annual bonuses, and a range of health-related benefits to employees and their families. We also provide a supportive and inclusive work environment that encourages professional growth and development.

At ICON, we are committed to providing a workplace free of discrimination and harassment. We welcome applications from diverse candidates and are an equal opportunity employer.



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