Bilingual Clinical Research Associate (CRA)
RemoteCanada
CanadaRemoteFull TimeEntry LevelBachelors DegreeSmall
Full TimeEntry LevelBachelors DegreeSmall
Job Summary
Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP. Maintain ongoing site correspondence and files, complete visit reports, and maintain study-related databases. Provide oversight and interaction with clinical research sites while reviewing patient charts and clinical data. Work remotely in Alberta or British Columbia with an average of 2 national assignments per month, utilizing customized PACE training and in-house physician-led therapeutic training.
Required Qualifications
- Bachelor's degree in science from an accredited university
- At least 1 year as a Clinical Research Associate or Clinical Research Coordinator
- Bilingual in English and French
- Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ICH E-6 guidelines and per Part-C, Division 5 of the Health Canada Food and Drug regulations
- Excellent interpersonal, written and verbal communication skills in English and French
- Strong attention to detail and organization skills
- Highly motivated, independent, flexible
- Ability to travel between 60-80%
- Ability to prioritize workload to meet timelines across multiple studies
- Proficient in Microsoft Office
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.