Clinical Scientist interpreting WES/WGS data and classifying variants for SeqOne, a clinical genomics company. Supporting rare - disease diagnostics through regulated, patient - centered genomic reporting.
About the role
- Clinical Research Associate monitoring clinical trials for ICON’s global healthcare research organization. Ensuring protocol, ICH-GCP, SOP, and regulatory compliance across investigative sites and remote work.
Responsibilities
- 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
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