TMF Lead
Hybrid · Mexico City, Mexico City, Mexico
Job Summary
TMF Lead responsible for overseeing TMF management across clinical trials, ensuring regulatory compliance and best practices; leads setup, maintenance, and oversight of the TMF, collaborates with cross-functional teams, conducts quality checks and audits, provides training on TMF processes, and drives continuous improvement in documentation practices. Requires a Bachelor's degree in life sciences or related discipline, proven TMF or clinical document management experience, solid regulatory knowledge, strong organizational and communication skills, and a commitment to equity and inclusion. Role is office-based in Mexico City with hybrid work arrangement.
Required Qualifications
- Bachelor's degree in life sciences, documentation management, or a related discipline
- Proven experience in TMF management or clinical trial document management
- Strong understanding of regulatory requirements and industry standards related to TMF and clinical documentation
- Excellent organizational skills and attention to detail
- Strong communication and interpersonal skills
- Commitment to promoting equity and inclusion in TMF management
- Willingness to work office based 3 times a week - Benito Juarez / Mexico City
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