Description
ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a Senior CRA / CRA II, 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 the progress of clinical studies and ensure compliance with regulatory requirements
- Conduct site visits and remote monitoring to ensure data quality and study integrity
- Collaborate with cross-functional teams to resolve issues and implement changes
Requirements:
- Bachelor's degree 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 (for level 2 role)
- Oncology monitoring experience preferred
- Ability to travel 70%
- Knowledge of ICH and local regulatory authority regulations regarding drug trials
- Bilingual (English/French) required
Benefits of Working in ICON:
- Competitive base salary and performance-related incentives
- Health and wellbeing programmes, including medical, dental, and vision coverage
- 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