Study Start Up Associate 2

ICON Clinical Research, LP

Not specified; benefits include annual leave, heal...
Regulatory document preparation and submission
Ethics committee and agency communications
Ich-gcp and local regulatory knowledge
The role involves leading the initiation of clinical trials while ensuring strict compliance with regulatory requirements

Job Summary

  • The role involves leading the initiation of clinical trials while ensuring strict compliance with regulatory requirements.
  • ICON offers a competitive salary along with diverse benefits including health insurance, retirement planning, and global employee assistance programs.
  • Candidates will collaborate with internal and external stakeholders to obtain necessary approvals and maintain accurate regulatory records.

Matching Summary

The role involves leading the initiation of clinical trials while ensuring strict compliance with regulatory requirements.

Salary

Not specified; Benefits include annual leave, health insurance, retirement planning, and flexible country-specific options

Skills & Requirements

Must-have

  • Regulatory document preparation and submission
  • Ethics committee and agency communications
  • ICH-GCP and local regulatory knowledge
  • Cross-functional stakeholder collaboration
  • Study start-up process management

Nice-to-have

  • Process improvement initiative participation
  • Strong organizational and project skills
  • Excellent communication and interpersonal abilities
  • Experience in innovative treatment advancement

Key Requirements

  • Bachelor's degree in life sciences or related field
  • Minimum 2 years experience in clinical research or regulatory affairs
  • Specific experience in study start-up activities

Work Rights

Not specified

Tailored Resume

Cover Letter