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 · Laval
The role focuses on enhancing client experiences by managing communications, hosting client visits, and acting as a conduit between strategic clients, Business Development, and Operations. Key duties include monitoring customer satisfaction programs, tracking project timelines, and managing contracts and invoices.
On-site · Montréal
The Client Manager acts as the primary host for client visits and serves as a conduit between strategic clients, Business Development, and Operations. They are responsible for managing customer satisfaction programs, monitoring budgets, and streamlining business processes to enhance efficiency.
Remote · Laval, Quebec, Canada
The Client Manager acts as the primary host for client visits and serves as a central conduit between strategic clients, Business Development, and Operations. They are responsible for managing project timelines, facilitating cross-functional meetings, and ensuring client satisfaction through proactive communication and issue resolution.
On-site · Laval
The Senior Regulatory Affairs Associate is responsible for preparing and submitting CTA and IND applications to regulatory authorities such as Health Canada and the FDA. They manage regulatory submissions, handle responses to information requests, and ensure compliance with current regulatory guidelines.
On-site · Laval
The scientist provides expertise in flow cytometry to manage, execute, and report on various assays while ensuring scientific quality and regulatory compliance. They act as a primary contact for clients and mentor analysts in the performance of bioanalytical studies.
Remote · Laval, Quebec, Canada
The Senior Regulatory Affairs Associate is responsible for preparing, reviewing, and submitting regulatory documents such as CTAs and INDs to agencies like Health Canada and the FDA. They also manage regulatory intelligence, maintain submission databases, and ensure compliance with evolving regulatory guidelines.
On-site · Laval
The Scientist will develop, plan, and manage flow cytometry and cell-based assays while ensuring compliance with regulatory standards like GLP and GCP. They will also act as a primary point of contact for clients and provide mentorship to laboratory analysts.
Hybrid · Laval
The Associate Scientist supports the Senior Scientist in bioanalytical tasks, including data compilation, trend analysis, and the drafting of validation plans and reports. They may also manage bioanalytical studies, oversee laboratory work for method development, and ensure compliance with SOPs and GLP/GCP guidelines.
Hybrid · Laval
The operator is responsible for performing sample injections for validation, production, and method development using mass spectrometry. They must monitor instrument performance, perform troubleshooting, and maintain laboratory documentation and equipment.
On-site · Laval
The Associate Scientist assists senior scientists with bioanalytical studies, including data review, method development, and validation. They are responsible for maintaining study timelines, documenting results, and ensuring compliance with GCP and GLP regulations.
On-site · Laval
The operator is responsible for performing daily batch injections in mass spectrometry, monitoring instrument performance, and conducting troubleshooting as needed. They also manage laboratory documentation, instrument optimization, and ensure compliance with SOP, GLP, and GCP standards.
On-site · Laval
Lead the regulatory strategy for non-clinical drug development programs, ensuring pharmacology and toxicology data support clinical phase transitions. Manage the preparation and critical review of non-clinical sections for regulatory dossiers such as IND, CTA, and NDA/BLA.
Hybrid · Montréal
Lead the design and implementation of enterprise data platforms and digital architecture to support AI and digital strategies in a regulated environment. Manage cross-functional teams of data scientists and engineers to deploy scalable digital solutions and ensure regulatory compliance.
On-site · Montréal
Lead the regulatory strategy for non-clinical drug development programs, ensuring pharmacology and toxicology data support clinical phase transitions. Manage the preparation and critical review of non-clinical sections for regulatory dossiers such as IND, CTA, and NDA/BLA.
On-site · Laval
Supervise all activities related to the arrival and reception of samples, including tracking deliveries and coordinating between quality control and technicians. Manage sample discrepancies, update IT systems, and ensure compliance with SOP, GLP, and GCP guidelines.
On-site · Laval
Ensure the quality control of generated data and laboratory work by verifying documentation accuracy and adherence to SOPs. Monitor laboratory quality according to GLP and regulatory requirements while supporting analysts in daily documentation processes.
Remote · Montreal, Quebec, Canada
The Vice President will lead the design and scaling of enterprise data platforms and AI strategies to improve business outcomes in a regulated environment. They are responsible for building high-performing teams and driving cross-functional digital transformation initiatives.
On-site · Laval
The QC reviewer is responsible for performing quality control on laboratory data and ensuring all batch documentation is accurate and compliant with SOPs. They also monitor laboratory quality according to GLP requirements and support analysts in daily documentation processes.
On-site · Laval
The Sample Logistics Coordinator oversees the reception and processing of incoming sample shipments while managing discrepancies and updating informatics systems. They are responsible for coordinating technician schedules, ensuring compliance with SOPs, and collaborating with study teams to resolve documentation issues.
Remote · Laval, Quebec, Canada
The Associate Director provides strategic regulatory guidance for nonclinical development programs, ensuring scientific rigor and compliance for IND, CTA, and NDA/BLA submissions. They lead cross-functional teams and serve as a subject matter expert during health authority interactions to facilitate efficient drug development.
