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 Biostatistician II leads studies by developing statistical analysis plans, generating randomization schedules, and creating summary tables and graphics. They are responsible for ensuring all analyses and documents comply with SOPs, GCP, and regulatory guidelines while coordinating with internal teams and clients.
On-site · Montréal
The Team Leader oversees the Participant Recruitment Agent team, ensuring all activities comply with study protocols and standard operating procedures. They are responsible for mentoring staff, monitoring call volumes, and managing the recruitment process for clinical trial volunteers.
On-site · Laval
The Office Clerk provides essential secretarial and administrative support, including document archiving, file management, and database maintenance. They also assist with conference room preparation and provide backup support for the reception desk.
Remote · Montreal, Quebec, Canada
The Participant Marketing Coordinator assists in clinical trial recruitment by managing social media campaigns, newsletters, and advertising materials. They also handle budget tracking, IRB submissions, and maintain communication with participants to ensure recruitment goals are met.
On-site · Montréal
The cleaner is responsible for performing general housekeeping and specialized cleaning duties to ensure a safe and presentable environment for staff and participants. This includes sanitizing facilities, managing inventory, and operating cleaning equipment according to established protocols.
Remote · Overland Park, Kansas, United States
The Workday HCM Analyst serves as a subject matter expert for Workday Time Tracking and Absence modules, responsible for system configuration, maintenance, and optimization. They translate business requirements into scalable solutions while ensuring data integrity, privacy, and effective user experience across the organization.
Hybrid · Montréal
The manager is responsible for overseeing the Quality Systems team, ensuring clinical trial data integrity, and maintaining compliance with GCP and SOPs. They will also lead process improvements, manage team performance, and participate in regulatory audits.
On-site · Laval
The technician is responsible for the end-to-end management of reference standards, including receipt, storage, inventory, distribution, and shipping. They must ensure all activities comply with standard operating procedures, good clinical practices, and good laboratory practices.
On-site · Laval
The QC Reviewer is responsible for performing quality control on laboratory data and documentation to ensure compliance with GLP and internal SOPs. They also guide analysts in documentation processes and assist in resolving quality issues or nonconformities identified during laboratory operations.
Hybrid · Laval
The Compliance Specialist supports the Bioanalytical Services department by managing regulated documentation and ensuring adherence to internal SOPs and regulatory guidelines. They also act as a quality representative to handle inquiries, audits, and deficiency letters while monitoring new regulatory developments.
On-site · Montréal
The Sample Management Coordinator manages biological samples collected during clinical trials while ensuring compliance with study protocols, GCP, and SOPs. They also act as a liaison between clinical operations teams and external vendors to ensure efficient sample processing and data integrity.
On-site · Laval
The technician is responsible for managing sample inventory, including reception, labelling, storage, and disposal of study materials. They must also perform Watson LIMS transactions and prepare samples for shipment in compliance with SOPs, GLPs, and GCPs.
On-site · Montréal
The Medical Equipment and Systems Specialist is responsible for coordinating, verifying, and maintaining equipment and system installations in compliance with study protocols and SOPs. They will manage calibration schedules, perform preventative maintenance, and ensure all equipment documentation meets quality and audit standards.
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.
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
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.
