Senior Study Start Up Associate

ICON Clinical Research, LP

Not specified; competitive within country; various...
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Conduct feasibility assessments and site identification
Manage site contract negotiation activities
Prepare regulatory and ethics submissions
** ICON Clinical Research is seeking a Senior Study Start Up Associate to support the initiation and progress of clinical trials. The role requires expertise in study start-up activities, regulatory compliance, and effective communication in both local languages and English. **

Job Summary

  • ICON is a world-leading healthcare intelligence and clinical research organization seeking a Senior Study Start Up Associate.
  • The role involves conducting feasibility assessments, site identification, and ensuring regulatory compliance for clinical trials.
  • Benefits include competitive salary, health insurance, retirement planning, and a global employee assistance program.

Matching Summary

Match Score: 75

** ICON Clinical Research is seeking a Senior Study Start Up Associate to support the initiation and progress of clinical trials. The role requires expertise in study start-up activities, regulatory compliance, and effective communication in both local languages and English. **

Salary

Not specified; Competitive within country; Various annual leave entitlements

Skills & Requirements

Must-have

  • Conduct feasibility assessments and site identification
  • Manage site contract negotiation activities
  • Prepare regulatory and ethics submissions
  • Review informed consent forms for patient safety

Nice-to-have

  • Fluency in local language and English
  • Experience in fast-paced clinical environments
  • Ability to collaborate with international teams

Key Requirements

  • Bachelor's degree or equivalent experience
  • At least 3 years of clinical study start-up experience
  • Fluency in local language and English

Work Rights

Not specified

Tailored Resume

Cover Letter