Remote TMF Specialist III — Quality & Submissions

KCR Placement

Ciudad de México

Remote

MXN 1,128,000 - 1,693,000

Full time

14 days+

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Benefits offered by this job

Annual leave entitlements
Health insurance offerings
Retirement planning options
Global Employee Assistance Programme (
Life assurance

Job summary

ICON Strategic Solutions in Mexico is seeking a TMF Specialist III to manage Trial Master File documentation for clinical trials. This home-based role supports sponsor contracts and cross-functional teams to ensure compliance and timely submissions.

You will oversee TMF documentation lifecycle, conduct quality checks, and provide guidance to stakeholders while collaborating with global teams. Travel about 5% may be required.

Qualifications

  • At least 3 years in clinical research or document management.
  • Bachelor's degree in life sciences or related field.
  • Strong attention to detail and ability to multitask.
  • Excellent written and verbal communication for cross-functional teams.
  • Willingness to travel ~5%.

Responsibilities

  • Manage TMF documentation per client requirements and ICON procedures.
  • Ensure completeness, accuracy, and timeliness of TMF documentation throughout trial lifecycles.
  • Collaborate with cross-functional teams to collect, review, and maintain documents for regulatory submissions.
  • Conduct quality checks and audits of TMF documents to ensure regulatory compliance.
  • Provide guidance to internal and external stakeholders on TMF-related matters.

Skills

TMF management
Regulatory documentation
Cross-functional communication
Attention to detail
Organizational skills

Education

Bachelor's degree in life sciences
Bachelor's degree in a related field

Job description

ICON Strategic Solutions in Mexico is seeking a TMF Specialist III to manage Trial Master File documentation for clinical trials. This home-based role supports sponsor contracts and cross-functional teams to ensure compliance and timely submissions.

You will oversee TMF documentation lifecycle, conduct quality checks, and provide guidance to stakeholders while collaborating with global teams. Travel about 5% may be required.

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