Start Up Specialist - 6 Month Assignment

ICON plc

UK
Not specified; competitive within country; include...
Hybrid
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 secure necessary approvals for study activation.
  • ICON offers a competitive salary, health insurance, retirement planning, and a diverse culture focused on well-being.

Matching Summary

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

Salary

Not specified; Competitive within country; Includes annual leave, health insurance, retirement planning, and flexible benefits

Skills & Requirements

Must-have

  • Leading regulatory document preparation
  • Coordinating ethics committee submissions
  • Managing study start-up activities
  • Collaborating with cross-functional teams

Nice-to-have

  • Process improvement initiative participation
  • Strong organizational and project management skills
  • 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 requirements
  • Must be based in the UK

Work Rights

Must be based in the UK

Tailored Resume

Cover Letter