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 Clinical Research Nurse oversees participant safety and consent while ensuring compliance with study protocols and Good Clinical Practices. Responsibilities include performing safety assessments, administering investigational products, and documenting adverse events.
On-site · Montréal
The Licensed Practical Nurse will oversee the safety of clinical trial participants and maintain safety equipment in compliance with study protocols and GCP. Responsibilities include performing clinical activities such as blood collection, medication administration, and monitoring participant adverse events.