Clinical Study Specialist

ICON plc

Warren, NJ, US
Not specified; bonus/equity: eligible depending on...
Hybrid
Bachelor's degree required
2 years industry experience
Global clinical trial support
The role involves organizing reports, scheduling meetings, and collating data for feasibility assessments to support global clinical trials

Job Summary

  • The role involves organizing reports, scheduling meetings, and collating data for feasibility assessments to support global clinical trials.
  • Candidates will manage study documents including informed consent forms and maintain versioning of study reference materials per SOPs.
  • ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a culture focused on inclusion and belonging.

Matching Summary

The role involves organizing reports, scheduling meetings, and collating data for feasibility assessments to support global clinical trials.

Salary

Not specified; Bonus/Equity: Eligible depending on role/performance; Benefits: Competitive salary, health insurance, retirement planning, EAP

Skills & Requirements

Must-have

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

Nice-to-have

  • Vendor management oversight
  • Process improvement initiatives
  • PowerPoint and Excel skills
  • Self-starter with minimal oversight

Key Requirements

  • Bachelor's Degree
  • Minimum 2 years industry experience
  • Experience supporting global trials
  • Knowledge of TMF and CTMS systems

Work Rights

Not specified

Tailored Resume

Cover Letter