Senior Clinical Research Associate
ICON · Montreal, Canada
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
This role involves monitoring clinical trial progress at investigative sites or remotely to ensure studies comply with protocols, SOPs, ICH-GCP guidelines, and regulatory standards. The position requires a bachelor's degree in a scientific or health-related field plus 1–3 years of clinical monitoring experience depending on level, with oncology background preferred and 70% travel expected.
What they're looking for
- Bachelor's degree in scientific or health-related field or equivalent education and clinical research experience
- 1+ years clinical monitoring experience for level 2 role; 3+ years for level 3 role
- Knowledge of ICH and local regulatory authority regulations for drug trials
- Legal authorization to work in United States or Canada without visa sponsorship
- Ability to travel 70%
- Oncology monitoring experience preferred
What you'll be doing
- Monitor progress of clinical studies at investigative sites or remotely
- Ensure clinical trials conducted, recorded, and reported per protocol and SOPs
- Verify compliance with ICH-GCP and applicable regulatory requirements
- Maintain documentation and regulatory standards throughout study conduct
Privacy & handoff
This role links to ICON's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.