Specialist/Associate, clinical research
QuebecTemps plein, Temporaire
FOP Consultants
1+ ansCandidates need a bachelor's or master's degree in a science or clinical field and one to five years of pharmaceutical, biotech or CRO experience, including monitoring visits. They must know ICH/GCP standards and Health Canada and FDA rules, be proficient in MS Office, and communicate well in French and English.
MS Office
Specialist/Associate, clinical trial
QuebecTemps plein, Temporaire
FOP Consultants
1+ ansCandidates need a bachelor's or master's degree in science, 1 to 5 years of industry experience (preferably in pharmaceuticals), and clinical research experience. They should know ICH/GCP and Health Canada and FDA rules, have TMF/eTMF experience, and write well in French and English.
eTMF, TMF, MS Office