- Paul Fenton, Vice-President of Pharmaceutical Processes and Technology
- Christophe Barcella, Vice-President of Pharmaceutical Development and Compliance
- Jean-Marie Constraint, Vice-President Finance and Administration
Montrium was founded on the basis of integrating expertise and know-how within a consortium of specialized consultants and partner firms. At the very center of this dynamic group are the following management team members:
Paul Fenton, Vice-President of Pharmaceutical Processes and Technology
Paul Fenton holds a degree in management from London Metropolitan University as well as an MBA in Technology Management from the Université du Québec à Montréal.
Paul has ten years industry experience at a senior management level in the development, deployment and management of computerized systems for use in regulated clinical trials. He co-founded eClinica in 2005, a company providing professional consultancy services in electronic clinical trials. He has worked on major clinical technology projects both in Europe and North America and has a strong background in CDISC and ICH standards as well as in the integration of systems and processes for clinical trials.
He is currently working with multiple pharmaceutical companies both in Canada and in the United States for the implementation and integration of computerized systems and processes such as EDC, CTMS, EDMS and electronic submissions in line with regulatory requirements and industry standards. He is a regular speaker at industry events and is actively involved in several projects for the development of clinical research standards and platforms.
Contact Paul Fenton at
Christophe Barcella, Vice-President of Pharmaceutical Development and Compliance
Christophe Barcella founded ClinVestigo, a Clinical Development consulting company in 2001 and heads up the Pharmaceutical Development and Compliance group at Montrium. Christophe graduated in Pharmacy Sciences and Quality Management at the Universities of Caen, Paris and Lyon, France. He started working in 1991 for different pharmaceutical firms, biotechnology companies, CROs, Academic Research Organizations including Production & Quality Control responsibilities at Sanofi-Pasteur and GSK as well as Clinical QA & Regulatory management at Quintiles Transnational.
With an in-depth international regulatory experience of drug/device development (Health Canada, FDA, EMEA) focused on oncology, CNS, immunology and dermatology; and advanced education in Quality Management, Christophe offers unique experience in the Clinical Research Field.
His expertise includes specialized training in eClinical Trials, Clinical Compliance, Computer Systems Validation, GLP, regulatory affairs, US IND and CTA submissions (Canada, EU member states), Clinical SOP development and Clinical Project Management (phase I-II, epidemiology). Christophe has also conducted over 400 GCP and GLP audits (Phase I to Phase IV) and Due Diligence audits worldwide including North America, South America, Europe and Middle East, for numerous pharmaceutical and allied industry clients.
Contact Christophe Barcella at
Jean-Marie Constraint, Vice-President Finance and Administration
Jean-Marie Constraint has over 15 years of financial and administrative management experience in various industries worldwide. Over time Jean-Marie has developed a strong business acumen and a vision of how to grow a successful business whilst also focusing on a good customer service and professionalism at all levels. These skills place him in good stead to manage Montrium’s business as it grows. Before moving to Canada in 2003 he held positions of responsibility in France, the United Kingdom and in Belgium.
Jean-Marie is the co-founder of eClinica Inc. and is also a co-founder of Montrium Inc.
Contact Jean-Marie Constraint at
