๐ŸŽ‰Welcome to JSS Medical Research! ๐ŸŽ‰


Are you searching for a powerhouse partner in product development? Look no further!


๐ŸŒŽ As a globally recognized Canadian-based CRO, we've got a world of experience under our belt. Over the past decade, we've navigated high-volume studies involving over 500,000 patients across 8,500 sites worldwide. You read that right - half a million patients!

๐ŸŽฏ With a proven track record across a broad spectrum of therapeutic areas from Oncology to Orthopedics, Infectious Diseases to Immunology, and everything in between, we've got you covered!

๐Ÿš€ Our dynamic team is always ready to adapt and respond swiftly to meet the evolving needs of regulatory authorities and healthcare providers. We're in it to win it, from Phase I to Phase IV of clinical trials.

๐Ÿ”ฌ We've got agreements with top-tier hospital sites and research centers across the globe and have mastered the art of remote and risk-based monitoring methodologies.

๐Ÿ’ช Choose JSS and get ready to turbocharge your product development with a dedicated, agile team that brings a wealth of knowledge, global reach, and innovative approaches to the table.

Join us on a journey to successful medical research! ๐Ÿš€๐ŸŒŸ

Ms. Boukas holds a Bachelor of Arts degree from McGill University as well as a Certificate in Technical Communications from Concordia University and has received compliance training from SNC Lavalin Pharma (SLP). She has over 25 years of experience in clinical settings and academic research including work with the McGill University Health Centre (MUHC), as well as in pharmaceutical research. She initially joined JSS Medical Research in 1998 as a Project Manager. In 2004 she participated in the development of the current Quality Assurance (QA) Program infrastructure under the mentorship of compliance specialists from SLP. Since that time, Ms. Boukas has managed the QA Program independently with compliance specialists acting as third-party auditors. Her experience and expertise provide a sound platform for implementing continuous improvements to processes, ensuring that the JSS Medical Research QA Program remains current with evolving industry standards including Good Clinical Practices (GCP), FDA 21 CFR Part 11, Good Documentation Practices (GDP), Health Canada, EMEA and other applicable regulatory requirements. The QA Program includes the Employee Training Program, management of standard operating procedures (SOPs), system validation, vendor qualification, CAPA management and auditing activities.

Currently, she is coordinating the expansion of the QA Program to encompass all global activities at JSS.

Our Latest News

Please take note that : โ€‹JSS will be attending BIO 2022 in San Diego from June 12โ€‘16
It will be a pleasure to receive your Visit at the PAVILLION DU QUร‰BEC booth EXโ€‘4323

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