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Job #02497

About our client Our client is a biotechnology company focused on developing new treatments for under-served markets in oncology and infectious diseases. Position Location Clinical Trials Coordinator Montreal, Quebec Salary Highly competitive package, commensurate with experience Responsibilities 1) Oversee the logistics of clinical trials in one of the two portfolios (oncology or infectious diseases) 2) Develop and maintain tracking systems, including document flow and invoices between the external partners (CROs, sites, etc.) 3) Oversee information retrieval and maintenance of the central clinical files (Trial Master File) 4) Follow-up with clinical sites and CROs 5) Document study team meetings 6) Coordinate and track study supplies 7) Prepare clinical documentation and maintain electronic documentation 8) Involve in meeting preparations and travel arrangements Requirements 1) University/college degree (B.Sc./B.A.) or certification in a related health profession from an accredited institution (e.g. Medical or Laboratory Technology) 2) 2+ years of experience in clinical research or relevant experience 3) Oncology or infectious disease experience 4) In-depth knowledge of clinical research, FDA, ICH/GCP guidelines 5) Ability to work effectively in a team environment with a high degree of professionalism 6) Flexible and detail-oriented 7) Ability to balance multiple priorities and work effectively in a fast-paced environment 8) Strong computer skills (i.e. Word, Excel, PowerPoint, etc.) 9) Good communication skills – English/French