Clinical Research Job at AstraZeneca, Canada
Elevate your career in global clinical trials with the Clinical Research Associate role at AstraZeneca. This Clinical Research Job at AstraZeneca Careers in Canada offers the opportunity to manage clinical studies, ensure regulatory compliance, and work closely with international research teams to bring life-saving treatments to patients.
About the Company:
AstraZeneca is a leading global biopharmaceutical company focused on discovering, developing, and delivering innovative medicines. Known for its collaborative culture and commitment to sustainability, AstraZeneca works across therapeutic areas to improve patient outcomes while addressing global health challenges.
Job Details:
- Job Role: Clinical Research Associate (CRA)
- Location: Quebec City, Quebec, Canada
- Job ID: R-247984
- Job Type: Full-Time
- Department: Clinical Research / Trials
- Salary Range: CAD 109,148 – 143,257 per year
- Bonus: Annual variable pay + long-term incentives
- Work Mode: Field-based with travel requirements
- Language Requirement: English & French (Bilingual)
Key Responsibilities:
- Manage and monitor clinical trial sites from initiation to closure as a Clinical Research Associate
- Ensure compliance with ICH-GCP guidelines and local regulations
- Conduct site qualification, monitoring visits, and data verification
- Train and support investigators and site staff in this Clinical Research Job at AstraZeneca Careers
- Handle study documentation, regulatory submissions, and reporting
- Perform Source Data Review (SDR) and Source Data Verification (SDV)
- Track patient recruitment and site performance in this Clinical Research Job in Canada
- Ensure timely reporting of adverse events and data queries
- Maintain study quality and inspection readiness
- Collaborate with local and global study teams
Educational Requirements for this Job:
- Bachelor’s degree in Life Sciences or related field
- Knowledge of clinical research and drug development processes
Skills Required:
- Strong understanding of ICH-GCP guidelines
- Knowledge of GMP/GDP and local regulations
- Clinical trial monitoring and data management skills
- Excellent communication and interpersonal skills
- Strong attention to detail and problem-solving ability
- Negotiation and collaboration skills
- Ability to manage multiple tasks and deadlines
- Familiarity with risk-based monitoring approaches
- Technical proficiency with clinical systems (CTMS, eTMF)
Benefits of the Clinical Research Job:
- High salary with bonus and equity incentives
- Global exposure in clinical research and trials
- Career growth in the pharmaceutical and CRO industries
- 4 weeks paid vacation + personal days
- Flexible benefits and retirement savings program
- Work in a top-ranked employer with a strong culture
- Opportunity to contribute to life-saving drug development
