Remote CRA II – Site Monitoring (Spain)

IQVIA

Madrid

Remote

EUR 36,000 - 48,000

Full time

43 hours ago
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Job summary

IQVIA Biotech in Spain is seeking a Clinical Research Associate to perform site monitoring visits, ensure GCP/ICH compliance, and support study execution across therapeutic areas. The role is home-based in Spain, with travel as required and close collaboration with trial sites to maintain quality, timelines, and regulatory documentation.

Ideal candidates will have 1.5+ years on-site monitoring experience and the ability to manage multiple sites and training efforts.

Qualifications

  • Bachelor's degree in scientific discipline or health care preferred.
  • 1.5+ years of on-site monitoring experience.
  • Ability to establish and maintain effective working relationships with sites, colleagues and clients.
  • Willingness to travel as required; valid driver's license preferred.
  • Equivalent combination of education and experience may be accepted.

Responsibilities

  • Perform site monitoring visits (selection, initiation, monitoring and close-out) complying with GCP/ICH.
  • Work with sites to recruit and enroll subjects per project needs.
  • Administer protocol training to sites and maintain regular communication.
  • Evaluate site conduct and regulatory compliance; escalate issues as needed.
  • Track regulatory submissions, recruitment, CRF completion, and data queries.
  • Maintain TMF/ISF and related study documentation.

Skills

Organizational skills
Time management
Problem-solving
Relationship building
Travel flexibility
Driver's license

Education

Bachelor's degree in scientific discipline or health care

Job description

IQVIA Biotech in Spain is seeking a Clinical Research Associate to perform site monitoring visits, ensure GCP/ICH compliance, and support study execution across therapeutic areas. The role is home-based in Spain, with travel as required and close collaboration with trial sites to maintain quality, timelines, and regulatory documentation.

Ideal candidates will have 1.5+ years on-site monitoring experience and the ability to manage multiple sites and training efforts.

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