Clinical Trials Associate

IQVIA

Singapore, Singapore
Good clinical practice (gcp) training
Clinical trial management system
Electronic trial master file
This is a unique opportunity for you to embark on your career in the clinical trial world and be trained by professionals from IQVIA

Job Summary

  • This is a unique opportunity for you to embark on your career in the clinical trial world and be trained by professionals from IQVIA.
  • In this role, you will be involved in the process of supporting clinical trials for various therapies at the country level, and be the liaison between the site and Contract Research Organization (CRO) / Pharmaceutical Company.
  • Learning Opportunities: Participate in comprehensive Good Clinical Practice (GCP) Training: Setting you up for success in Clinical Research.

Matching Summary

This is a unique opportunity for you to embark on your career in the clinical trial world and be trained by professionals from IQVIA.

Skills & Requirements

Must-have

  • Good Clinical Practice (GCP) Training
  • Clinical Trial Management System
  • electronic Trial Master File
  • regulatory documents collection
  • site activation process
  • site management department

Nice-to-have

  • Effective Minute taking
  • Managing Challenging Communications
  • Cross-cultural Awareness
  • interpersonal communication skills
  • organizational skills

Key Requirements

  • Bachelor of Science in Life Sciences or Healthcare
  • Biosciences, Pharmacy related disciplines
  • Good command of English
  • Good word processing skills
  • knowledge of MS Office applications
  • General awareness clinical trial environment
  • drug development process

Work Rights

Not specified

Tailored Resume

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