Sponsor - Ready Trials with a Global Delivery Model
Pharmaxi MRM is a USA-based Contract Research Organization and a joint venture between Pharmaxi Ltd (Europe) and MRM BioEnt (UAE) - delivering end-to-end clinical trial services with strong compliance, reliable operations, and regional access across Europe and MENA.
What we do
Full-service CRO support across the trial lifecycle - from early regulatory strategy and protocol development to site activation, monitoring, data management, biostatistics, safety, and closeout.
Clinical Operations
Site start-up, monitoring, TMF oversight, vendor coordination
Regulatory Affairs
IND-enabling support, agency-ready submissions, lifecycle management
Medical Writing
Protocols, IB, CSR, SAP, CTD modules, narratives
Data & Biostatistics
EDC build, data cleaning, SDTM/ADaM support, analyses
Pharmacovigilance
Case processing, literature screening, aggregate reports
Quality & Audits
SOPs, CAPA, vendor qualification, audit readiness
Expert Team
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Pascal Brabant
Pascal Brabant brings more than 35 years of experience in clinical research and clinical operations. With medical training and prior service in the Canadian Armed Forces, he began his clinical career at the Montreal Heart Institute, where he spent 10 years involved in cardiovascular medicine and clinical research. He later held senior management roles in global CROs including Covance and Keyrus Life Science, and served as a therapeutic lead at Wyeth Pharmaceuticals Canada, overseeing programs in cardiovascular, internal medicine, and infectious diseases. He subsequently held the position of Director of Clinical Operations at Methylene. Over the past 15 years, Mr. Brabant has worked as a clinical operations consultant, supporting sponsors and research organisations across North America and globally. He currently collaborates with Pharmaxi MRM, providing strategic guidance in global clinical operations with a particular focus on North American activities.
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Hélène Dubreuil
Hélène Dubreuil is a registered nurse with more than 30 years of experience in healthcare and clinical research. She began her career with 10 years of clinical nursing experience within the Quebec Health Network before transitioning to clinical research. She spent six years as a clinical research associate with major organisations including Quintiles and Pfizer, gaining extensive experience in site monitoring and clinical trial oversight. Over the past 20 years, Ms. Dubreuil has worked as an independent consultant specialising in site monitoring, monitoring team leadership, and quality assurance site auditing. She currently supports Pharmaxi MRM by providing expertise in site monitoring, management of monitoring teams, and site auditing to ensure high standards of clinical trial conduct and regulatory compliance.
Expert Team
Post
Post
Pascal Brabant
Pascal Brabant brings more than 35 years of experience in clinical research and clinical operations. With medical training and prior service in the Canadian Armed Forces, he began his clinical career at the Montreal Heart Institute, where he spent 10 years involved in cardiovascular medicine and clinical research. He later held senior management roles in global CROs including Covance and Keyrus Life Science, and served as a therapeutic lead at Wyeth Pharmaceuticals Canada, overseeing programs in cardiovascular, internal medicine, and infectious diseases. He subsequently held the position of Director of Clinical Operations at Methylene. Over the past 15 years, Mr. Brabant has worked as a clinical operations consultant, supporting sponsors and research organisations across North America and globally. He currently collaborates with Pharmaxi MRM, providing strategic guidance in global clinical operations with a particular focus on North American activities.
Post
Post
Hélène Dubreuil
Hélène Dubreuil is a registered nurse with more than 30 years of experience in healthcare and clinical research. She began her career with 10 years of clinical nursing experience within the Quebec Health Network before transitioning to clinical research. She spent six years as a clinical research associate with major organisations including Quintiles and Pfizer, gaining extensive experience in site monitoring and clinical trial oversight. Over the past 20 years, Ms. Dubreuil has worked as an independent consultant specialising in site monitoring, monitoring team leadership, and quality assurance site auditing. She currently supports Pharmaxi MRM by providing expertise in site monitoring, management of monitoring teams, and site auditing to ensure high standards of clinical trial conduct and regulatory compliance.
