Tmf Lead

ICON Clinical Research, LP

Mexico City, Mexico
On-site
Tmf management processes
Regulatory requirements
Clinical trial documentation
ICON Clinical Research is seeking a TMF Lead in Mexico City to oversee Trial Master File management processes while ensuring compliance with regulatory standards. The ideal candidate should possess experience in clinical trial document management, strong communication skills, and a commitment to promoting an inclusive work environment

Job Summary

  • As a TMF Lead at ICON, you will be responsible for overseeing the Trial Master File (TMF) management processes, ensuring compliance with regulatory requirements and best practices in clinical trials.
  • Your expertise will be essential in maintaining the integrity of the TMF and supporting efficient document management throughout the trial lifecycle.
  • In addition to your competitive salary, ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work-life balance opportunities.

Matching Summary

Match Score: 85

ICON Clinical Research is seeking a TMF Lead in Mexico City to oversee Trial Master File management processes while ensuring compliance with regulatory standards. The ideal candidate should possess experience in clinical trial document management, strong communication skills, and a commitment to promoting an inclusive work environment.

Skills & Requirements

Must-have

  • TMF management processes
  • regulatory requirements
  • clinical trial documentation
  • TMF quality checks and audits
  • continuous improvement strategies

Nice-to-have

  • promoting equity and inclusion

Key Requirements

  • Bachelor's degree in life sciences, nursing, or business administration
  • Proven experience in TMF management
  • Strong understanding of regulatory requirements
  • Excellent organizational skills and attention to detail

Work Rights

Not specified

Tailored Resume

Cover Letter