Quicker go/no-go decisions with integrated preclinical, clinical, bioanalytical, manufacturing, and CRO services.
Laval, Quebec
Outsourcing made easy with a one-stop solution to early-phase drug development. We are an integrated drug development solution company, offering pharmaceutical and biotechnology companies a proven, flexible approach that removes the need for multiple service providers during the early stages of drug development. Whether for one study or an end-to-end program, we help you reach critical decision-making milestones sooner by improving speed and ease from lead candidate selection to clinical proof of concept, and beyond. When partnering with Altasciences, you can experience up to 40% in time savings thanks to our integrated, one-stop solution offering. We strive to create a true partnership with our clients, our partners, and our colleagues that enables a mutually supporting relationship built on a combination of excellent science and solid communication. Helping sponsors get better drugs to the people who need them, faster, for over 30 years. Our full-service offering is always tailored to your specific research needs: - Preclinical research - Clinical pharmacology - Drug formulation - Manufacturing and analytical services - Bioanalysis - Program management - Medical writing - Biostatics - Data management - And so much more!
On-site · Montréal
The Licensed Practical Nurse will screen clinical study participants by performing technical activities such as blood collection, safety measurements, and data collection. They are responsible for ensuring participant eligibility and compliance with study protocols, GCP, and SOPs.
On-site · Montréal
The Clinical Research Nurse oversees the safety and consent of clinical trial participants while ensuring compliance with study protocols and GCP. Key duties include safety monitoring, administering investigational products, and maintaining emergency equipment records.
On-site · Montréal
The Licensed Practical Nurse oversees the safety of clinical trial participants and maintains safety equipment in compliance with protocols and GCP. Key duties include performing safety assessments, blood collection, administering medication, and monitoring adverse events.