Clinical Research Associate 2, Iqvia

IQVIA Inc

Base: $71,900.00 - $189,000.00 annually; bonus/equ...
On-site clinical trial monitoring experience
Good clinical practice (gcp) knowledge
International conference on harmonization (ich) guidelines
The role involves performing site monitoring visits to ensure studies are conducted according to protocol and regulatory requirements

Job Summary

  • The role involves performing site monitoring visits to ensure studies are conducted according to protocol and regulatory requirements.
  • Candidates will work with sites to drive subject recruitment plans and manage ongoing project expectations through regular communication.
  • IQVIA offers a competitive base pay range of $71,900.00 to $189,000.00 annually along with potential incentive plans and benefits.

Matching Summary

The role involves performing site monitoring visits to ensure studies are conducted according to protocol and regulatory requirements.

Salary

Base: $71,900.00 - $189,000.00 annually; Bonus/Equity: Incentive plans may be offered; Benefits: Health, welfare, and other benefits included

Skills & Requirements

Must-have

  • On-site clinical trial monitoring experience
  • Good Clinical Practice (GCP) knowledge
  • International Conference on Harmonization (ICH) guidelines
  • Site initiation and close-out visit execution
  • Subject recruitment plan management

Nice-to-have

  • Phase 1 clinical trial experience
  • CNS therapeutic area expertise
  • GLP-1/Obesity/Diabetes background
  • Cardiovascular clinical trial experience
  • Strong organizational problem-solving skills

Key Requirements

  • Bachelor's Degree in scientific discipline or healthcare preferred
  • At least 1 year of on-site monitoring experience required
  • Proficiency in Microsoft Word, Excel, PowerPoint, and mobile devices

Work Rights

Not specified

Tailored Resume

Cover Letter