Clinical Study Specialist

ICON Clinical Research, LP

Warren, NJ, US
Not specified; bonus, stock, + commissions may be ...
Hybrid
Bachelor's degree required
Minimum 2 years industry experience
Global clinical trial support experience
The role involves organizing reports, scheduling meetings, and collating data for global clinical trials across multiple regions

Job Summary

  • The role involves organizing reports, scheduling meetings, and collating data for global clinical trials across multiple regions.
  • Candidates must have a Bachelor's degree and at least two years of industry experience supporting global trials in NA, LAM, EU, APAC, or India.
  • ICON offers competitive benefits including health insurance, retirement planning, and a global employee assistance program focused on well-being.

Matching Summary

The role involves organizing reports, scheduling meetings, and collating data for global clinical trials across multiple regions.

Salary

Not specified; Bonus, Stock, and Commissions may be eligible based on performance; Competitive salary offered

Skills & Requirements

Must-have

  • Bachelor's Degree required
  • Minimum 2 years industry experience
  • Global clinical trial support experience
  • TMF and CTMS proficiency
  • SharePoint and Excel skills
  • ICF review experience

Nice-to-have

  • Vendor management oversight experience
  • Process improvement initiative mindset
  • Self-starter with minimal oversight
  • Solution-oriented approach
  • Strong written and verbal communication

Key Requirements

  • Bachelor's Degree
  • 2+ years industry experience
  • Experience with TMF and CTMS
  • ICF review experience

Work Rights

Not specified

Tailored Resume

Cover Letter