Clinical Research Associate 2, Iqvia

IQVIA

Durham, United States
Base: $57,500.00 - $226,800.00; bonus/equity: ince...
On-site monitoring experience
Glp-1/obesity/diabetes or cardiovascular trials
Gcp and ich guidelines
Perform monitoring and site management work to ensure sites conduct studies and report data as required by protocol, regulations, and sponsor requirements

Job Summary

  • Perform monitoring and site management work to ensure sites conduct studies and report data as required by protocol, regulations, and sponsor requirements.
  • Administer protocol and study training to sites, establish communication lines, and manage project expectations and issues.
  • Manage study progress by tracking regulatory submissions, recruitment, CRF completion, and data query resolution.

Matching Summary

Perform monitoring and site management work to ensure sites conduct studies and report data as required by protocol, regulations, and sponsor requirements.

Salary

Base: $57,500.00 - $226,800.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits

Skills & Requirements

Must-have

  • On-site monitoring experience
  • GLP-1/Obesity/Diabetes or Cardiovascular trials
  • GCP and ICH guidelines
  • Site recruitment plan management
  • CRF completion and submission

Nice-to-have

  • Phase 1 experience
  • Site financial management
  • Effective time management skills
  • Problem-solving skills

Key Requirements

  • At least 1 year on-site monitoring experience
  • Bachelor's Degree in scientific discipline or health care preferred
  • Good knowledge of GCP and ICH guidelines
  • Proficiency in Microsoft Word, Excel, and PowerPoint

Work Rights

Not specified

Tailored Resume

Cover Letter