Senior / Clinical Research Associate

IQVIA UK

Wilayah Persekutuan Kuala Lumpur, Malaysia
Hybrid
Site selection and monitoring
Protocol and training administration
Regulatory submission tracking
This role offers opportunities for career progression into areas like operations management, dedicated customer solutions, and project management with dedicated mentoring and structured reviews

Job Summary

  • This role offers opportunities for career progression into areas like operations management, dedicated customer solutions, and project management with dedicated mentoring and structured reviews.
  • Responsibilities include performing site visits, supporting subject recruitment, administering protocol training, evaluating site quality, and managing progress tracking.
  • IQVIA provides access to cutting-edge technology, opportunities to work on global projects, and a supportive environment for building a flexible, meaningful, and fulfilling career.

Matching Summary

This role offers opportunities for career progression into areas like operations management, dedicated customer solutions, and project management with dedicated mentoring and structured reviews.

Skills & Requirements

Must-have

  • site selection and monitoring
  • protocol and training administration
  • regulatory submission tracking
  • case report form completion
  • applicable clinical research regulatory requirements

Nice-to-have

  • career development opportunities
  • flexible work schedules
  • cutting-edge in-house technology
  • collaborating with diverse colleagues

Key Requirements

  • University degree in scientific discipline or healthcare
  • At least 1 year of on-site monitoring experience
  • Good knowledge of GCP
  • Excellent command of English language
  • Flexibility to travel

Work Rights

Not specified

Tailored Resume

Cover Letter