Regulatory Affairs Expert

hace 1 mes


Ciudad de México, Ciudad de México Worldwide Clinical Trials A tiempo completo
About the Role

We are seeking a highly skilled Regulatory Affairs Expert to join our team at Worldwide Clinical Trials.

Job Description

In this role, you will be responsible for planning, initiating and tracking documents required for regulatory submissions. You will also be involved in collecting essential documents, reviewing country/site/EC requirements, and communicating status, risks and actions related to start-up activities and maintenance when applicable.

Requirements
  • Strong organizational and management skills
  • Proactive approach to identifying potential issues in the process and anticipating solutions
  • Thorough understanding of country level cultural norms and local healthcare systems
  • Easily adjusts to a changing environment and prioritizes adapt between detailed and strategic activities while maintaining delivery timelines and quality
What We Offer

A competitive salary of $85,000 - $110,000 per annum, depending on experience.

The opportunity to work with a global team of experts in the clinical trials industry.

A dynamic and values-driven work environment that empowers employees to take ownership and make a real difference.


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