Senior Clinical Research Associate

Job Description:

• Monitor the progress of clinical studies at investigative sites or remotely
• Ensure clinical trials are conducted, recorded, and reported according to the protocol
• Ensure compliance with standard operating procedures (SOPs), ICH-GCP, and applicable regulatory requirements
• Support clinical research for pharmaceutical, biotechnology, medical device, government, and public health organizations

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
• 1+ years of clinical monitoring experience or equivalent combination of education and experience required for the level 2 role
• 3+ years of clinical monitoring experience required for a level 3 role
• Oncology monitoring experience preferred
• Ability to travel 70%
• Knowledge of ICH and local regulatory authority regulations regarding drug trials
• Legally authorized to work in the United States or Canada
• Must not require, now or in the future, sponsorship for employment visa status
• Bilingual English/French required

Benefits:

• Competitive base salary
• Performance related incentives
• Medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways
• Supportive policies and wellbeing initiatives
• Reasonable accommodations during the recruitment process