Senior Clinical Research Associate
$31,200–$31,200 year
On-siteMontréal, Quebec, Canada or Burlington, Ontario, Canada
Montréal, Quebec, Canada or Burlington, Ontario, 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, standard operating procedures, ICH-GCP, and all applicable regulatory requirements. 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 without requiring sponsorship for employment visa status
- Bilingual (English/French)
Desired Qualifications
- 3+ years of oncology monitoring experience
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