Leading our project teams to address the specific needs of each of our clients, VCLS Senior Consultants provide their expertise in the regulatory, medical and strategic domains, while maintaining personal contacts with the regulatory agencies.

Senior Team

Frédéric Pailloux, Pharm.D.

Head, Swiss Operations Senior Director, Drugs & Biologics

Frédéric Pailloux, Pharm.D.

Head, Swiss Operations Senior Director, Drugs & Biologics

Frederic Pailloux manages projects involving the design and implementation of global regulatory strategies for the development, evaluation and marketing of small molecules and biologics.



Gopalan Narayanan, M.D.

Vice-President, Disruptive Biologics

Gopalan Narayanan, M.D.

Vice-President, Disruptive Biologics

Within VCLS, Dr Narayanan provides leadership in the area of complex and disruptive biologics.



Carey Anderson, M.Sc.

Senior Director, Regulatory Science

Carey Anderson, M.Sc.

Senior Director, Regulatory Science

As a Senior Director, Regulatory Science, Carey assists international clients in the design and implementation of global product development plans and associated regulatory strategies.



Chris Wilson, B.Sc., M.Sc., MTOPRA

Senior Director, Drugs and Biologics and Head of Medical Writing

Chris Wilson, B.Sc., M.Sc., MTOPRA

Senior Director, Drugs and Biologics and Head of Medical Writing

As Senior Director, Chris manages the design and implementation of global regulatory strategies for the development, evaluation and marketing of small molecules and biologics.



Christophe Amiel, M.Sc.

Senior Director, Medical Devices & Combination Products

Christophe Amiel, M.Sc.

Senior Director, Medical Devices & Combination Products

Christophe Amiel is heading the design and implementation of regulatory strategy as Senior Director within Voisin Consulting Life Sciences.



David Lucking, B.Sc.

Senior Director, Regulatory Science, Drugs & Biologics

David Lucking, B.Sc.

Senior Director, Regulatory Science, Drugs & Biologics

David Lucking is currently Senior Director, Regulatory Science, Drugs and Biologics at Voisin Consulting Life Sciences.



Delphine Decker, M.Sc.

Senior Director, Regulatory Science, Clinical Trials

Delphine Decker, M.Sc.

Senior Director, Regulatory Science, Clinical Trials

Delphine Decker plays a major role in Voisin Consulting Life Sciences (VCLS) activities related to Clinical Trials Application and Project Management.



Marie Deneux, Ph.D.

Senior Director, Drugs and Biologics

Marie Deneux, Ph.D.

Senior Director, Drugs and Biologics

Marie assists international clients in the design and implementation of global product development plans and associated regulatory strategy, in particular in the area of rare diseases.



Marielle Fournier, Pharm.D.

Senior Director, Drugs, Devices & Combination Products

Marielle Fournier, Pharm.D.

Senior Director, Drugs, Devices & Combination Products

Marielle has several responsibilities within the management of projects involving the design and implementation of global regulatory strategies.



Peter Embley, PGDPRA, MTOPRA

Senior Director, Regulatory Science, Drugs & Biologics

Peter Embley, PGDPRA, MTOPRA

Senior Director, Regulatory Science, Drugs & Biologics

Peter brings over 19 years applied industrial and commercial biopharmaceutical experience to his role, including 17 years in Regulatory Affairs.



Florence Bine-Scheck, MD

Senior Medical Director

Florence Bine-Scheck, MD

Senior Medical Director

As Senior Medical Director with VCLS, Florence is Head of the Non Clinical and Clinical Development group.



Zsuzsanna Tamas, M.D.

Senior Medical Officer

Zsuzsanna Tamas, M.D.

Senior Medical Officer

As Senior Medical Officer and member of VCLS Non Clinical and Clinical team, Zsuzsanna provides assistance and advice to VCLS clients on the clinical aspects of their projects.



Amanda Gibbons, Ph.D

Director, Regulatory Science, Drugs & Biologics

Amanda Gibbons, Ph.D

Director, Regulatory Science, Drugs & Biologics

Amanda is responsible for the design and implementation of strategic development plans, particularly on Chemistry Manufacturing and Control (CMC) aspects of biological products.



Carlo Chiavaroli, Ph.D

Director, Nonclinical & Early Clinical Development

Carlo Chiavaroli, Ph.D

Director, Nonclinical & Early Clinical Development

With 20 years in diverse areas of the pharmaceutical industry, Dr. Carlo Chiavaroli has considerable expertise in the drug development process.



Carole Jones, B.Sc., M.B.A

Director, Market Access

Carole Jones, B.Sc., M.B.A

Director, Market Access

Carole joined VCLS in January 2017 to support the development of the Market Access service.



Delphine Kazancigil, Pharm.D, M.Sc

Director, Regulatory Science, Drugs & Biologics

Delphine Kazancigil, Pharm.D, M.Sc

Director, Regulatory Science, Drugs & Biologics

Delphine is an experienced regulatory affairs professional who has an in-depth knowledge of the European (EU) legislation and regulatory requirements.



Emmanuel Prades, M.Sc.

Director, Clinical Operations

Emmanuel Prades, M.Sc.

Director, Clinical Operations

With 20 years in diverse areas of the pharmaceutical industry, Emmanuel Prades has considerable expertise in project management for the clinical operations processes.



Laura Millichamp, Ph.D.

Director, CMC & Quality

Laura Millichamp, Ph.D.

Director, CMC & Quality

Laura Millichamp is responsible for the management of projects involving the development of Chemistry Manufacturing and Controls (CMC).



Sylvie Le Glédic, Ph.D.

Director, Medical Devices & IVD

Sylvie Le Glédic, Ph.D.

Director, Medical Devices & IVD

Sylvie Le Glédic is in charge of the design and implementation of global regulatory strategies for the development and registration of in vitro diagnostics medical devices (IVDs).



Tim Adetona, M.Sc., D.PH

Director, Drugs & Nutraceuticals

Tim Adetona, M.Sc., D.PH

Director, Drugs & Nutraceuticals

Tim has a broad regulatory expertise of close to 20 years’ experience in addressing and obtaining regulatory authorization for various life-science products including drugs, biologics and innovative nutritional products.



Alexandra Beumer Sassi, PhD, RAC

Associate Director, CMC

Alexandra Beumer Sassi, PhD, RAC

Associate Director, CMC

As an Associate Director, Chemistry, Manufacturing and Controls at VCLS, Alexandra (Alex) is responsible for providing CMC and regulatory consulting services to clients.



Susan Carter, M.Sc.

Associate Director, Regulatory Science

Susan Carter, M.Sc.

Associate Director, Regulatory Science

As Assoicate Director, Regulatory Science, Susan provides scientific and regulatory advice to clients for the development of small molecules and biologics particularly with regards to rare diseases.



Cécile F. Rousseau, Ph.D.

Associate Director

Cécile F. Rousseau, Ph.D.

Associate Director

At VCLS, Cécile is involved in the nonclinical and clinical areas, her expertise encompassing medical devices, cellular therapy, gene therapy, and in vitro diagnostics.



Anastacia M. Bilek, Ph.D.

Associate Director, Medical Devices & Combination Products

Anastacia M. Bilek, Ph.D.

Associate Director, Medical Devices & Combination Products

Anastacia “Stacie” Bilek is a Director, Medical Devices and Combination products.



Cécile Henrot, M.Sc.

Associate Director, Regulatory Clinical Trials

Cécile Henrot, M.Sc.

Associate Director, Regulatory Clinical Trials

Cécile Henrot specializes in clinical trials within VCLS, and manages the submissions to European competent authorities, ethics committees and other regulatory bodies as appropriate.



Emmanuelle Sabbah-Petrover, Ph.D.

Associate Director, Complex Biologics

Emmanuelle Sabbah-Petrover, Ph.D.

Associate Director, Complex Biologics

As Associate Director at Voisin Consulting Life Sciences, Emmanuelle manages projects involving cell, gene & tissue-based medicinal products (“ATMPs”); from non-clinical to clinical phases, both in Europe & the US.



Nicolas Martin, M.Sc.

Associate Director, Vigilance Operations

Nicolas Martin, M.Sc.

Associate Director, Vigilance Operations

Nicolas co-heads the Vigilance Operations, to support in managing the group strategy and resources, overseeing QA activities, business development and knowledge management.



Valerie Arnaudinaud-Lignier, Ph.D.

Associate Director, CMC & Quality

Valerie Arnaudinaud-Lignier, Ph.D.

Associate Director, CMC & Quality

Valerie Anaudinaud-Lignier is responsible for the management of projects involving the development of Chemistry Manufacturing and Controls (CMC).