Senior Clinical Site Manager (Canada)

As a Senior Clinical Site Manager, you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.

• Responsible for all kinds of site visits (e.g. Selection / Initiation / Monitoring / Close-out / Motivational / Support) and sites’ performance regarding set-up, conduct and data collection
• Primary contact for sites regarding study-related issues.
• Responsible for the early engagement with Key Opinion Leaders (KOLs)/ sites / patients organizations and key contact point for these throughout the study.
• Develop, communicate, and execute Site Engagement Strategy/Plan working closely with the Sponsor Clinical Team and key internal stake holders throughout the life cycle of the clinical trials
• Support Sponsor clinical team in coordinating and executing site engagement activities by understanding the competitive landscape, capturing trial hurdles and using motivational tactics to ensure timely delivery of clinical trials
• Engage, evaluate and develop a global network of high performing sites through coordinated, consistent interactions using multiple communication channels to create awareness of sponsor and its activities thereby increasing their desire to partner with Sponsor
• Develop & maintain relationships with site engagement organizations; assist in identification of high performing sites and key opinion leaders that can contribute to sponsor forums, boards and/or discussions
• Interact/train new investigators to work on sponsor clinical trials

• A minimum of 5 years of experience in the Pharmaceutical, Biotechnology, and/or CRO industry is required with a preference towards individuals who have experience in site engagement or an investigator facing role (e.g. clinical project manager, study director/coordinator, clinical research associate, patient/site engagement companies)

• S., M.S. degree in a life science/biological related field preferred. At least three years experience in monitoring of trials in clinical development environment, preferably in phase 2-4 if responsibility for phase 2-4.
• Strong Knowledge of GCP and ICH Guidelines.