Senior Clinical Research Associate 1 - Sponsor Dedicated

IQVIA Inc

Spain
2 years on-site monitoring experience
Good clinical practice gcp knowledge
International conference harmonization ich guidelines
The role involves performing site selection, initiation, monitoring, and close-out visits for clinical trials

Job Summary

  • The role involves performing site selection, initiation, monitoring, and close-out visits for clinical trials.
  • Candidates will support subject recruitment plans while ensuring data integrity according to GCP and ICH guidelines.
  • IQVIA offers resources for career growth, flexible work schedules, and an attractive benefits package including a mobile phone.

Matching Summary

The role involves performing site selection, initiation, monitoring, and close-out visits for clinical trials.

Skills & Requirements

Must-have

  • 2 years on-site monitoring experience
  • Good Clinical Practice GCP knowledge
  • International Conference Harmonization ICH guidelines
  • Spanish and English language command

Nice-to-have

  • Flexible work schedules
  • World-class training and mentoring
  • Diverse therapeutic area exposure
  • Strong problem-solving skills

Key Requirements

  • University degree in scientific discipline or health care
  • Driver's license class B
  • Excellent computer skills including MS Office

Work Rights

Not specified

Tailored Resume

Cover Letter