Description
We are seeking a Senior Clinical Research Associate (CRA) to join our team in Montreal. As a CRA, you will 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.
Responsibilities:
- Monitor clinical studies and ensure compliance with regulations and protocols
- Conduct site visits and remote monitoring
- Review and report clinical data
- Collaborate with cross-functional teams
Qualifications:
- Bachelor's degree in a scientific or health-related field
- 1+ years of clinical monitoring experience (or equivalent)
- Oncology monitoring experience preferred
- Ability to travel 70%
- Knowledge of ICH and local regulatory authority regulations
- Fluent in French and English
Benefits of Working at ICON:
- Competitive salary and benefits package
- Health and wellbeing programmes
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities