Clinical Research Technician conducting participant - facing clinical trial activities at Altasciences’ Montreal site. Handling samples, safety measurements, IP administration, and questionnaires.
About the role
- Clinical Scientist designing trials, analyzing data, and supporting regulatory submissions at ICON, a global clinical research organization advancing new therapies.
Responsibilities
- Design and implement clinical trial protocols, ensuring adherence to scientific and regulatory standards
- Conduct data analysis and interpretation to derive insights supporting study objectives
- Collaborate with cross-functional teams to ensure effective study execution and data quality
- Engage with stakeholders to communicate findings and contribute to scientific discussions
- Assist in preparing regulatory submissions, study reports, and scientific publications
Requirements
- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Experience in clinical research or a related scientific role, with a strong understanding of clinical trial processes
- Excellent analytical skills and proficiency in data interpretation and statistical analysis
- Strong communication and collaboration skills, with the ability to work effectively in interdisciplinary teams
- Detail-oriented and committed to maintaining high standards of data integrity and quality
- Willingness to travel as required (approximately 20%)
- Legal right to work in the country where the role is based
Benefits
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including 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
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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