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
- Senior Clinical Trial Manager leading clinical trial delivery for ICON, a global healthcare intelligence and research organization. Overseeing start-up, execution, compliance, risks, budgets, and closeout.
Responsibilities
- Lead the operational delivery of assigned clinical trials, ensuring milestones, timelines, budget expectations, and quality standards are achieved
- Drive study start-up activities, site activation, enrollment strategies, and study execution through database lock
- Provide oversight of study progress, monitoring activities, clinical metrics, and site performance
- Develop and implement effective study oversight plans, monitoring strategies, and risk mitigation approaches
- Identify operational challenges and proactively implement solutions to ensure successful study delivery
- Build and maintain strong relationships with sponsors, investigators, vendors, and cross-functional stakeholders
- Review study performance metrics and provide regular status updates and reporting
- Support, mentor, and collaborate with Clinical Research Associates (CRAs) and other study team members
- Ensure all clinical trial activities comply with protocol requirements, ICH-GCP guidelines, and applicable regulatory requirements
Requirements
- Bachelor's degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or another relevant scientific discipline, or an equivalent combination of education and experience
- Significant Clinical Trial Management experience within a CRO (preferred), pharmaceutical, or biotechnology environment
- Demonstrated ability to successfully lead and deliver clinical studies from start-up through closeout
- Strong understanding of clinical trial operations, ICH-GCP, and applicable regulatory requirements
- Experience managing study timelines, budgets, vendors, and cross-functional stakeholders
- Proven ability to identify risks, solve complex operational challenges, and drive study execution
- Prior monitoring experience preferred
- Experience managing global and/or complex clinical trials preferred
- Ability to travel up to 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
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