Senior / Clinical Research Associate

IQVIA UK

Singapore, Singapore
Hybrid
On-site monitoring experience
Good knowledge of gcp
Clinical research regulatory requirements
At IQVIA, we do not believe in a ‘career ceiling’ and offer opportunities in operations management, dedicated customer solutions, project management and more

Job Summary

  • At IQVIA, we do not believe in a ‘career ceiling’ and offer opportunities in operations management, dedicated customer solutions, project management and more.
  • You will be exposed to cutting-edge in-house technology and have opportunities to work on global projects and trials.
  • The company supports flexible work schedules and provides programs to build technical skills, therapeutic knowledge, and regulatory updates.

Matching Summary

At IQVIA, we do not believe in a ‘career ceiling’ and offer opportunities in operations management, dedicated customer solutions, project management and more.

Skills & Requirements

Must-have

  • On-site monitoring experience
  • Good knowledge of GCP
  • Clinical research regulatory requirements
  • Site selection and initiation
  • Monitoring and close-out visits
  • Data query resolution
  • MS Office proficiency

Nice-to-have

  • Organizational and time management skills
  • Problem-solving skills
  • Effective communication skills
  • Flexible travel availability
  • Mentoring and career development
  • Working on global trials

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter