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 Inventory Coordinator supports daily receiving, stocking, and inventory control activities to ensure material availability for site operations. This role maintains compliance with SOPs and GXP standards while managing stock rotation, cycle counts, and shipment coordination.
On-site · Montréal
The Supervisor manages the recruitment team, overseeing performance, scheduling, and training to ensure clinical trial activities comply with protocols and SOPs. They also coordinate with marketing, handle sponsor communications, and track departmental KPIs to ensure operational success.
On-site · Montréal
The Facilities Maintenance Technician performs routine preventative maintenance on HVAC and critical systems while managing special projects and site repairs. They are responsible for 24/7 emergency help line coverage and general upkeep of company facilities.
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.
Remote · Montreal, Quebec, Canada
The Participant Marketing Coordinator manages clinical trial recruitment activities, including social media campaigns, newsletters, and advertising materials. They also ensure compliance with study protocols and GCP while maintaining participant databases and tracking recruitment metrics.
On-site · Montréal
The Clinical Research Technician executes clinical trial activities in compliance with study protocols, Good Clinical Practices, and Standard Operating Procedures. They are responsible for sample handling, safety measurements, participant interaction, and maintaining work-station cleanliness.
Remote · Laval, Quebec, Canada
The Procurement Specialist I supports sourcing activities for laboratory supplies, raw materials, and equipment while ensuring compliance with regulatory standards like GxP and FDA. They are responsible for processing purchase orders, negotiating contracts, and analyzing spend data to optimize costs and maintain supply continuity.
Remote · Overland Park, Kansas, United States
The Biostatistician II acts as the lead for clinical studies, managing the biostatistics team and ensuring all analysis and documentation comply with regulatory standards. They are responsible for developing statistical analysis plans, generating randomization schedules, and overseeing the quality control of clinical trial data.
On-site · Laval
The Archiving Assistant is responsible for maintaining archives, scanning documents, and performing clerical duties for the Archivist. They will also manage database updates and handle the physical manipulation of archiving storage containers.
Hybrid · Laval
The Quality Assurance Coordinator is responsible for generating efficient schedules for the QA team and assigning staff to study submissions based on timelines and availability. They must also proactively identify risks of non-compliance and communicate audit deliverable delays to operations.
On-site · Montréal
The Customer Service Representative manages incoming inquiries from prospective clinical trial participants and assesses their initial eligibility for studies. They are responsible for scheduling appointments, maintaining participant records, and ensuring all interactions adhere to study protocols and confidentiality standards.
On-site · Laval
The Senior Research Scientist will lead the development and optimization of robust bioanalytical methods using LC-MS/MS to support various therapeutic modalities. They will also oversee sample preparation, interpret complex data, and ensure all documentation complies with regulatory standards.
On-site · Montréal
The cleaner is responsible for maintaining a clean, safe, and presentable environment by performing general housekeeping, specialized cleaning, and sanitization tasks. They also manage cleaning supplies inventory and report any maintenance issues or hazards to the supervisor.
On-site · Laval
The Office Clerk provides secretarial and administrative support, including document archiving, file management, and database maintenance. They also assist with conference room preparation and act as a back-up for the receptionist.
On-site · Laval
The Scientist will oversee immunogenicity study conduct, including assay development, validation, and sample analysis. They serve as the primary scientific contact for clients and ensure all bioanalytical work complies with regulatory standards.
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 while ensuring compliance with GLP, GCP, and SOP guidelines.
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 contribute to quality management initiatives, including responding to audits, deficiency letters, and monitoring new industry regulations.
On-site · Laval
The Sample Logistics Coordinator oversees the reception and processing of incoming sample shipments while maintaining accurate documentation and informatics systems. They are responsible for managing sample discrepancies, coordinating with study designers, and ensuring all work complies with GLP, GCP, and SOP standards.
Remote · Laval, Quebec, Canada, Montreal, Quebec, Canada
The specialist will develop and execute proactive talent attraction and sourcing strategies to build pipelines for scientific, operational, and corporate roles. They will manage a portfolio of requisitions from intake to hire while partnering with hiring managers and marketing to enhance employer branding.
On-site · Montréal
The Team Leader oversees the Participant Recruitment Agent team, ensuring all recruitment activities comply with study protocols and Good Clinical Practices. They are responsible for mentoring staff, monitoring call volumes, and managing the scheduling of clinical trial screening appointments.
