Senior Clinical Research Associate
$31,200–$31,200 year
On-siteMontréal, Quebec, Canada
Montréal, Quebec, CanadaOn-siteFull Time$31,200–$31,200 yearSenior LevelBachelors DegreeEnterprise
Full TimeSenior LevelBachelors DegreeEnterprise
Job Summary
Monitor the progress of clinical studies at investigative sites or remotely, ensuring trials are conducted, recorded, and reported in accordance with the protocol, SOPs, ICH-GCP, and applicable regulatory requirements. Verify data accuracy and resolve protocol deviations while maintaining compliance with standard operating procedures. This role requires a Bachelor's degree in a scientific or health-related field, 1+ years of clinical monitoring experience (3+ preferred for oncology), and the ability to travel 70%. Applicants must be legally authorized to work in the United States or Canada without sponsorship.
Required Qualifications
- Bachelor's degree, or its international equivalent in a scientific or health-related field
- 1+ years of clinical monitoring experience or equivalent combination of education and experience
- 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
- No requirement for employment visa sponsorship
- Bilingual (English/French)
Desired Qualifications
- 3+ years of ONCOLOGY MONITORING EXPERIENCE
- Professional of health status (e.g., registered nurse)
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