Senior CRA

Monitor the progress of clinical studies, either at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.

• Bachelor's degree, or its international equivalent in a scientific or health-related field or an equivalent combination of education and clinical research experience, particularly in a study coordinator or nursing role
• 1+ years of clinical monitoring experience or equivalent combination of education and experience is required for the level 2 role
• 3+ years is required for a level 3
• ONCOLOGY MONITORING EXPERIENCE PREFERRED
• Ability to travel 70%
• Knowledge of ICH and local regulatory authority regulations regarding drug trials
• To qualify, applicants must be legally authorized to work in the United States or Canada, and should not require, now or in the future, sponsorship for employment visa status
• BILINGUE (ANGLAIS/FRANÇAIS) REQUIS

ONCOLOGY MONITORING EXPERIENCE PREFERRED

• Various annual leave entitlements
• A range of health insurance offerings to suit you and your family’s needs
• Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
• Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
• Life assurance
• Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.