Clinical Research Associate, Sponsor Dedicated, Iqvia

IQVIA UK

United States
Base: $71,900.00 - $169,300.00; bonus/equity: ince...
Onsite
Onsite monitoring experience
Cardiovascular/renal/metabolic expertise
Oncology expertise
Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor requirements

Job Summary

  • Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor requirements.
  • Evaluate the quality and integrity of study site practices related to proper protocol conduct and adherence to regulations, escalating quality issues as appropriate.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

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

Salary

Base: $71,900.00 - $169,300.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits

Skills & Requirements

Must-have

  • Onsite monitoring experience
  • Cardiovascular/Renal/Metabolic expertise
  • Oncology expertise
  • Neurology expertise
  • Good Clinical Practice (GCP)
  • ICH guidelines

Nice-to-have

  • Adapt and drive subject recruitment
  • Effective time management skills
  • Effective financial management skills
  • Establish effective working relationships

Key Requirements

  • 1-2 years onsite monitoring experience
  • Bachelor's Degree in scientific discipline or health care preferred
  • Basic knowledge of clinical research regulatory requirements
  • Proficiency in Microsoft Word, Excel and PowerPoint

Work Rights

Not specified

Tailored Resume

Cover Letter