Sr. Cra

ICON Clinical Research, LP

East Coast, US
Not specified; competitive salary offered; range o...
Fully remote
Oncology monitoring experience required
2-5 years cra 2 or 5+ years sr cra experience
Knowledge of ich gcp guidelines
The role involves implementing and monitoring clinical trials to ensure compliance with sponsor obligations and ICH Good Clinical Practice guidelines

Job Summary

  • The role involves implementing and monitoring clinical trials to ensure compliance with sponsor obligations and ICH Good Clinical Practice guidelines.
  • Candidates will be responsible for site startup activities, including regulatory document collection, informed consent review, and budget negotiations.
  • ICON offers a competitive salary, diverse benefits focused on well-being, and a culture dedicated to inclusion and belonging.

Matching Summary

The role involves implementing and monitoring clinical trials to ensure compliance with sponsor obligations and ICH Good Clinical Practice guidelines.

Salary

Not specified; Competitive salary offered; Range of additional benefits included

Skills & Requirements

Must-have

  • Oncology monitoring experience required
  • 2-5 years CRA 2 or 5+ years Sr CRA experience
  • Knowledge of ICH GCP guidelines
  • Site startup and feasibility experience
  • Source document verification skills

Nice-to-have

  • Budget negotiations experience preferred
  • Subject matter expert leadership skills
  • Complex study assignment capability
  • Advanced negotiating skills for clinical tasks

Key Requirements

  • Undergraduate degree in clinical, science, or health field
  • Licensed healthcare professional or equivalent work experience
  • 5+ years clinical monitoring experience for Sr level
  • Fluent English reading, writing, and speaking
  • Legal authorization to work in the United States without sponsorship

Work Rights

Must be legally authorized to work in the US

Tailored Resume

Cover Letter