Clinical Research Associate monitoring Canadian clinical trials for Parexel, a global clinical research organization. Managing site relationships, compliance, data quality, and study delivery.
About the role
- Remote Clinical Scientist supporting oncology clinical trials at ICON Strategic Solutions. Assisting study teams with monitoring, adjudication, imaging reconciliation, and protocol management.
Responsibilities
- Assist the CS Protocol Lead and study team with the clinical/scientific conduct of clinical studies, including adjudication support, medical monitoring, imaging data reconciliation preparation, meeting materials, and protocol deviation management
- Support a single study or multiple studies
- Lead a study with limited scope, such as Survival Follow-up
- Interact with internal and external stakeholders, including study sites and committees, in support of clinical study objectives
Requirements
- BS/BA/MS/PhD in Life Sciences with 2+ yrs relevant career experience
- If no degree in Life Sciences, must have significant experience in clinical development (>5 years)
- Pharmaceutical experience beneficial but not required
- Experience in Oncology required
- 2 years medical monitoring experience highly preferred
- ePro experience a plus
- Demonstrated oral and written communication skills
- Excel and PP experience required
- Ability to travel up to 15% (might include international travel)
- Legally authorized to work in the United States and/or Canada
- Should not require, now or in the future, sponsorship for employment visa status
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
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