Senior Clinical Research Associate, Early Clinical Development

IQVIA Inc

East Coast, US
Base: $87,200.00 - $169,300.00; bonus/equity: ince...
Not specified (assumed to be flexible based on industry norms).
Phase 1 clinical trial experience
On-site monitoring experience
Gcp and ich guidelines knowledge
IQVIA Inc is seeking a Senior Clinical Research Associate (CRA) for their Early Clinical Development team, focusing on candidates with Phase 1 experience located on the East Coast of the US. The role involves monitoring clinical trial sites, ensuring compliance with protocols and regulatory standards, and contributing to the integrity of clinical research data

Job Summary

  • The role involves conducting all types of site visits including selection, initiation, monitoring, and close-out in alignment with GCP and ICH guidelines.
  • Candidates will collaborate with site staff to implement subject recruitment strategies that align with project timelines and enrollment goals.
  • IQVIA is a leading global provider of clinical research services committed to accelerating the development of innovative medical treatments.

Matching Summary

Match Score: 85

IQVIA Inc is seeking a Senior Clinical Research Associate (CRA) for their Early Clinical Development team, focusing on candidates with Phase 1 experience located on the East Coast of the US. The role involves monitoring clinical trial sites, ensuring compliance with protocols and regulatory standards, and contributing to the integrity of clinical research data.

Salary

Base: $87,200.00 - $169,300.00; Bonus/Equity: Incentive plans and bonuses may be offered; Benefits: Range of health and welfare benefits included

Skills & Requirements

Must-have

  • Phase 1 clinical trial experience
  • On-site monitoring experience
  • GCP and ICH guidelines knowledge

Nice-to-have

  • Cross-functional team collaboration
  • Subject recruitment strategy implementation
  • Financial management support

Key Requirements

  • Bachelor's degree in life sciences or health-related field
  • At least 1.5 years of on-site monitoring experience
  • Located on the East Coast of the US

Work Rights

Not specified

Tailored Resume

Cover Letter