Associate Start Up & Regulatory Manager

Ivivamedical

Flexible, United States
Site activation and maintenance activities
Regulatory submissions and documentation
Clinical research processes and regulations
Support the delivery of site activation and maintenance activities for assigned studies or multi-protocol programmes

Job Summary

  • Support the delivery of site activation and maintenance activities for assigned studies or multi-protocol programmes.
  • Prepare, review, and track regulatory and contractual documentation, ensuring timely execution.
  • This is an excellent opportunity for someone looking to step into greater responsibility within Regulatory & Start-Up.

Matching Summary

Support the delivery of site activation and maintenance activities for assigned studies or multi-protocol programmes.

Skills & Requirements

Must-have

  • site activation and maintenance activities
  • regulatory submissions and documentation
  • clinical research processes and regulations
  • cross-functional team collaboration
  • clinical systems and Microsoft Office

Nice-to-have

  • leadership capability development
  • international study exposure
  • solution-focused mindset
  • strong working relationships

Key Requirements

  • Bachelor’s degree in a related scientific or clinical field
  • 2–3 years relevant experience in clinical research
  • Around 3 years clinical research experience
  • Exposure to leadership or coordination responsibilities

Work Rights

Not specified

Tailored Resume

Cover Letter