Senior Clinical Research Associate 1 - Sponsor Dedicated

IQVIA UK

Not specified; not specified; attractive benefits ...
Good clinical practice (gcp) knowledge
International conference on harmonization guidelines
Site selection and initiation visits
The role involves performing site selection, initiation, monitoring, and close-out visits while ensuring regulatory compliance

Job Summary

  • The role involves performing site selection, initiation, monitoring, and close-out visits while ensuring regulatory compliance.
  • Candidates will gain direct experience with a customer while enjoying the stability of a leading global contract research organization.
  • The position 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 while ensuring regulatory compliance.

Salary

Not specified; Not specified; Attractive benefits package

Skills & Requirements

Must-have

  • Good Clinical Practice (GCP) knowledge
  • International Conference on Harmonization guidelines
  • Site selection and initiation visits
  • Subject recruitment plan development
  • Case report form completion tracking

Nice-to-have

  • Flexible work schedule support
  • World-class training and mentoring
  • Diverse therapeutic area experience
  • Effective client relationship building
  • Strong problem-solving skills

Key Requirements

  • University degree in scientific discipline or health care
  • At least 2 years of on-site monitoring experience
  • Excellent command of Spanish and English language
  • Driver's license class B required
  • Very good computer skills including MS Office

Work Rights

Not specified

Tailored Resume

Cover Letter