Associate Clinical Project Manager, Sponsor Dedicated

IQVIA Inc

Base: $68,400.00 - $232,800.00; bonus/equity: ince...
2 years clinical trial management experience
Drafting and managing informed consent process
Managing site selection and patient recruitment strategies
This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout

Job Summary

  • This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout.
  • Candidates must have expertise in drafting informed consent processes, managing site selection, and driving risk-based mitigation plans.
  • The position requires two years of clinical trial management experience within a role accountable for driving local trial activities at the regional level.

Matching Summary

This sponsor-dedicated role provides country-level oversight of clinical trials from study start-up through database lock and closeout.

Salary

Base: $68,400.00 - $232,800.00; Bonus/Equity: Incentive plans may be offered; Benefits: Range of health and welfare benefits available

Skills & Requirements

Must-have

  • 2 years clinical trial management experience
  • Drafting and managing informed consent process
  • Managing site selection and patient recruitment strategies
  • Knowledge of ICH GCP and local regulatory standards
  • Driving risk-based mitigation plans

Nice-to-have

  • Strong written and verbal communication skills
  • Experience with MS Office applications
  • Ability to handle conflicting priorities
  • Cross-cultural collaboration awareness
  • Understanding of project financials

Key Requirements

  • Bachelor's Degree in life sciences or related field
  • 2 years clinical trial management experience
  • Intermediate knowledge of clinical trial conduct principles
  • Strong command of English language

Work Rights

Must reside in the same country where the job is located

Tailored Resume

Cover Letter