About us

Advancing Clinical Research with Expertise & Commitment

We are dedicated to helping life sciences industry conduct efficient, compliant, and impactful clinical trials. With deep industry expertise and a flexible, collaborative approach, we provide tailored consulting services to support sponsors (pharmaceutical, biotechnology, medical device, and non-profit organisations) and CROs.

Who We Are

Hey, I am Zoé Moksi – Clinical Research Consultant and founder of ZMF RESOURCES, a consultancy company delivering high quality services to sponsors and CROs. I am a Neuroscientist by education and have over 20 years of experience in clinical research, I’ve contributed to clinical studies across all clinical phases, various treatment modalities, and therapeutic areas.

My experience includes:

• All phases of clinical trial development
• Complex study designs and diverse patient populations
• Diverse treatment modalities, including drugs, biological products, drug-device combinations, Class III medical devices…
• Broad therapeutic area, including but not limited to:
  • Cardiovascular
  • Central Nervous System (CNS) / Neurology
  • Immune-mediated / Inflammatory Diseases
  • Infectious Diseases
  • Neglected Diseases
  • Oncology & Hematology
  • Pediatrics
  • Rare Diseases
  • Respiratory
  • Substance Abuse / Addiction
  • Urology

What We Do

Through ZMF RESOURCES, I work closely with sponsors and service providers to design, plan, execute, monitor, and report clinical trials in France and globally.

To expand our capabilities, we collaborate with a network of trusted consultants, offering flexibility and tailored expertise to meet the unique needs of each project.

With a strong commitment to quality, compliance, and operational excellence, we help sponsors streamline clinical trial operations and deliver impactful, reliable results.

Our Journey

2012 – ZMF RESOURCES SAS was founded in Paris by Zoé Oumel Moksi, specializing in consulting in Clinical Trial Operations and Project Management.

2014 – Offices moved to Annecy (France) – Proximity to Geneva provides easy access to Swiss companies and international markets via Geneva International Airport.

2017 – Patrick Faramaz joined as CTO, strengthening our IT capabilities and expanding our services to include the development of custom digital solutions, technology consulting and training.

2020 – Introduced Clinical Quality Assurance & GCP Auditing services to help organizations enhance regulatory compliance and inspection readiness.

2024 – Introduced pragmatic Agentic AI services.

2026 – Expanded our digital services with agentic coding capabilities.

Today – We continue to learn, evolve and pursue excellence to better support sponsors in bringing innovative therapies to patients and contributing to a healthier world.

Why Choose Us?

• Solide Industry Experience – 20+ years of experience navigating the complexities of clinical trials and regulatory frameworks.
• Proven Track Record – Successful collaborations with pharmaceutical, biotech, medical device, CRO and non-profit organizations, delivering rreliable, high-quality results.
• Global Expertise – Consultants with work experience across all continents, adapting to diverse regulatory landscapes.
• Commitment to Excellence – Our approach is rooted in Quality, integrity, and precision.
• Client-Centric – We work as an extension of your team, fostering long-term relationships based on trust and transparency.
• Commitment to Continuous Learning – Staying ahead of industry trends, evolving regulations, and best practices, ensuring our services meet the highest quality standards.

Let’s collaborate!

Need dedicated resources? (e.g., project manager, monitor, regulatory expert to integrate into your team?)
Need end-to-end execution of key services? (e.g., audit, QMS gap analysis, SOP development?)

We adapt to your needs and provide the right strategic and operational support for your clinical trial goals.

Thanks for stopping by and for reading our story.