Site Specialist

ICON plc

Chennai, India
Not specified; competitive within country; include...
3+ years clinical trial experience
Study start-up process knowledge
Contract management skills
ICON is a world-leading healthcare intelligence and clinical research organization seeking a Site Specialist II to support global clinical development

Job Summary

  • ICON is a world-leading healthcare intelligence and clinical research organization seeking a Site Specialist II to support global clinical development.
  • The role involves critical responsibilities including study start-up activities, informed consent form customization, and contract negotiation for clinical sites.
  • Candidates will benefit from a competitive salary, health insurance, retirement planning, and a diverse culture focused on well-being and work-life balance.

Matching Summary

ICON is a world-leading healthcare intelligence and clinical research organization seeking a Site Specialist II to support global clinical development.

Salary

Not specified; Competitive within country; Includes various annual leave and health insurance offerings

Skills & Requirements

Must-have

  • 3+ years clinical trial experience
  • Study start-up process knowledge
  • Contract management skills
  • ICF customization experience
  • IRB/EC submission processes

Nice-to-have

  • Global team collaboration
  • Flexible shift availability
  • Excellent written communication
  • Attention to detail in documentation

Key Requirements

  • Bachelor's degree in life sciences or business
  • 3+ years of experience in clinical trials
  • Understanding of study start-up and maintenance

Work Rights

Not specified

Tailored Resume

Cover Letter