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Altasciences

Source d’offres vérifiée

Quicker go/no-go decisions with integrated preclinical, clinical, bioanalytical, manufacturing, and CRO services.

Laval, Quebec

Research Services
1 001 à 5 000 personnes

À propos

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!

Postes ouverts

Technicien(ne) de niveau II d'entretien des installations- FR

Sur place · Montréal

Responsible for general maintenance of Altasciences sites, including HVAC systems, basic plumbing, painting, and facility repairs. Coordinates with external providers and manages the 24/7 emergency assistance line on a rotation basis.

Superviseur, centre d'appels- FR

Sur place · Montréal

The Call Center Supervisor coordinates recruitment activities and manages the recruitment team to ensure clinical trial timelines are met. They are responsible for staff training, performance evaluations, and ensuring compliance with study protocols and Good Clinical Practices.

Coordonnateur(trice), assurance qualité- FR

Sur place · Laval

The Quality Assurance Coordinator manages the collaboration between operational and scientific staff and the QA department by establishing schedules and assigning personnel to study submissions. They are responsible for updating planning software and proactively reporting risks regarding delivery deadlines.

Assistant(e) aux archives - contrat de 12 mois- FR

Sur place · Laval

The Archives Assistant is responsible for managing archives, scanning documents, and performing administrative tasks for the archivist. Key duties include updating databases, preparing for inspections, and handling physical archiving boxes.

Spécialiste technique en Gestion des échantillons- FR

Sur place · Laval

Supervise the sample management technician team to ensure quality, efficiency, and integrity of study materials and samples. Manage storage optimization, traceability in Watson LIMS, and compliance with SOP, GLP, and GCP guidelines.