Clinical Research Associate, Sponsor Dedicated, Oncology Or Immunology

IQVIA

Multiple Locations
Base: $69,800.00 - $226,800.00; bonus/equity: ince...
Gcp and ich guidelines
Site monitoring visits
Recruitment plan development
Conduct selection, initiation, monitoring, and close-out visits in line with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines

Job Summary

  • Conduct selection, initiation, monitoring, and close-out visits in line with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
  • Collaborate with sites to develop, drive, and track recruitment plans, enhancing predictability and meeting project needs.
  • Provide protocol training and maintain regular communication with sites to manage expectations and address issues.

Matching Summary

Conduct selection, initiation, monitoring, and close-out visits in line with Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

Salary

Base: $69,800.00 - $226,800.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Health and welfare and/or other benefits may be offered

Skills & Requirements

Must-have

  • GCP and ICH guidelines
  • Site monitoring visits
  • Recruitment plan development
  • Protocol training
  • Trial Master File (TMF)
  • Investigator's Site File (ISF)

Nice-to-have

  • Mentoring clinical staff
  • Effective time management
  • Problem-solving skills
  • Interpersonal skills

Key Requirements

  • 2.5 years on-site monitoring experience
  • Oncology or immunology preference
  • BS Degree in scientific discipline or healthcare

Work Rights

Not specified

Tailored Resume

Cover Letter