Site Start Up Specialist

ICON plc

Not specified; competitive salary mentioned; vario...
Leading regulatory document preparation
Coordinating ethics committee submissions
Managing study start-up activities
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.
  • Candidates will coordinate with internal and external stakeholders to obtain necessary approvals for study activation.
  • ICON offers a competitive benefits package including health insurance, retirement planning, and a global employee assistance program.

Matching Summary

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

Salary

Not specified; Competitive salary mentioned; Various annual leave entitlements; Health insurance offerings; Retirement planning offerings

Skills & Requirements

Must-have

  • Leading regulatory document preparation
  • Coordinating ethics committee submissions
  • Managing study start-up activities
  • Ensuring ICH-GCP compliance

Nice-to-have

  • Process improvement initiative participation
  • Cross-functional team collaboration
  • Willingness to travel approximately 5%

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
  • Strong understanding of ICH-GCP and local regulatory guidelines

Work Rights

Not specified

Tailored Resume

Cover Letter