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Altasciences

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

Laval, Quebec

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Research Services
1,001–5,000 people

About

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!

Open positions

Financial Analyst

On-site · Laval

About The Role The Financial Analyst is responsible for supporting the month-end closing process, performing accounts reconciliations and analysis and supporting the team for reporting financial statements to Management. The financial analyst is also responsible for supporting the implementation of internal controls. What You'll Do Here The tasks specifically assigned to the financial analyst may vary according to business needs. Without limitations, these may include: Support month end process and reconciliations within deadlines and procedures; Prepare monthly analysis of consolidated a…

Scientific Project Manager

On-site · Laval

About The Role The Scientific Project Manager leads project teams, manages key relationships with internal and external stakeholders, supports logistics, and drives timelines and communication to ensure successful execution. The Scientific Project Manager develops and proactively manages project timelines and is responsible for the scope of work including third party vendor involvement. The Scientific Project Manager adequately evaluates probability and impact of risk, develops and implements risk management plans to mitigate effect on project objectives and deliverables, and effectively nav…

PK Scientist I

On-site · Laval

About The Role The PK Scientist I is responsible for gathering and synthesizing scientific information, performing PK analysis, and providing high-quality documents to support sponsors' research programs. What You'll Do Here Serve as the PK representative or nonclinical principal investigator or contributing scientist on assigned project teams. Review of protocols for studies of moderate complexity. Prepare and/or review data transfer agreements (DTAs). Prepare and/or review protocol deviation impact assessments, sample inventory summaries (SIS), and PK population determinations. Prepare a…

Clinical Quality Control Associate II

On-site · Montréal

About The Role The Clinical Quality Control Associate is responsible for the quality control (QC) review of clinical trial data and working with the Quality Systems team to complete QC related tasks.  The Clinical Quality Control Associate will conduct tasks performed within compliance of study protocol, Good Clinical Practices (GCP) and Standard Operating Procedures (SOPs). What You’ll Do Here Report, track and escalate (if necessary) errors and/or trends that may require re-training, as required by location. Compile data and maintain computerized files and/or update deviation tracking sy…

Technician I, Sample Management

On-site · Laval

About The Role The Technician I, Sample Management is responsible for conducting sample management activities, including sample and material inventory, service requests, disposal, and shipment. This role supports the organization and maintenance of storage areas and ensures accurate handling and tracking of samples in accordance with established procedures and regulatory requirements. What You'll Do Here Execute transactions in LIMS and electronic inventory systems for all sample movements. Ensure proper storage conditions and accurate location of samples and study materials. Generate and…

Technician, Sample Management (Student / On-Call)

On-site · Laval

About The Role The Technician, Sample Management (Student / On-Call) is responsible for conducting sample management activities, including sample and material inventory, service requests, disposal, and shipment. This role supports the organization and maintenance of storage areas and ensures accurate handling and tracking of samples in accordance with established procedures and regulatory requirements. What You'll Do Here Execute transactions in LIMS and electronic inventory systems for all sample movements. Ensure proper storage conditions and accurate location of samples and study mater…

Medical Administrative Assistant

On-site · Montréal

About The Role The Medical Administrative Assistant provides administrative assistance to Clinical Principal Investigator and to the Director, Clinical Operations. The Medical Administrative Assistant gathers and compiles data in order to generate various reports. What You'll Do Here Scheduling the Clinical Principal Investigator’s for all dosing activities and screening activities. Book meetings and resources (for both internal and external clients). Assemble all documentation for trials. Prepare and ensure the follow-up with needed signature from Principal Investigator , Sub-Investigator…

IT Technician II

On-site · Laval

About The Role An IT Technician II is responsible for supporting Altasciences’ users in their usage of the tools provided by the IT department such as computers, telephones, software, laptops, mobile phones, etc. An IT Technician II responds to and tracks user requests and solutions via an automated Helpdesk System. The IT Technician II will support the more junior technicians and act as a point of escalation if required.    What You'll Do Here The computer technician provides accurate and creative solutions to user problems.  Enhance and develop quality support methods and communication sk…

Data Manager II

On-site · Laval

About The Role The Data Manager II supports sponsors’ research programs by contributing to the data cleaning efforts needed to provide clean, analyzable clinical data proficiently and independently. What You’ll Do Here Perform data management cleaning activities including listing review, issuing, and closing queries, and external vendor data reconciliation per protocol, department and client standards, and International Conference on Harmonisation (ICH) Good Clinical Practice (GCP) guidelines. Ensure all fields are entered as appropriate and validation checks are complete. Appropriately tr…

Advisor, Internal Communications - Temporary contract

On-site · Laval

About The Job The Advisor, Internal Communications will be a key contributor to the Internal Communications department whose objective is to develop internal communications strategies and implement plans and tools to support the company's business strategies, promote its organizational culture and increase employee engagement. On a day-to-day basis, the Advisor, Internal Communications will be responsible for supporting internal client groups with their communications needs by creating engaging and effective content tailored to the various internal channels to maximize the reach of messages…

QC Reviewer (BSD)

On-site · Laval

About The Role The QC Reviewer (BSD) is responsible to perform the quality control for data generated and work conducted in the laboratory. What You'll Do Here Ensures that all batch related documentation is completed accurately and in a timely manner by the analysts and that all procedures are respected as per the company’s SOPs. Based on training QC reviewer can draft study documents for BPI review such as Memo to File, SOP/Protocol/Study Plan deviations., perform quality control batch review by performing multi-batch trend analysis, and compile study documentation, Based on training, pr…

Analyst I, Laboratory (BSD)

On-site

About The Role The Analyst is responsible bench work and documentation based on their assignment to the laboratory. Ensures that analyses are performed in accordance with appropriate SOPs. What You'll Do Here Responsible for experiments at the bench based on training and competencies can be assigned conduct validation and/or sample analysis. Apply appropriately the standard operating procedure (SOP) for both method-specific and general processes and ensure completeness and accuracy of documentation. Respect general SOPs Complete supplementary information forms as needed to complete documen…

QC Reviewer, Sample Management (12-month contract)

On-site · Laval

About the role The Quality Control Reviewer, Sample Management Department, is responsible for the quality control review of documentation related to the Sample Management team. He/she also conducts audits within the team to ensure that quality standards are met. He/she participates in the drafting and/or revision of standard operating procedures for sample management and glass washing. What you'll be doing here Perform 100% quality control on documentation generated by the sample management team. Responsible for quality within the sample management team. Perform audits within the team: dev…

Senior Analyst LBA

On-site · Laval

About The Role The Senior Analyst is responsible bench work and documentation based on their assignment to the laboratory. Ensures that analyses are performed in accordance with appropriate SOPs. What You’ll Do Here Technical assay expert in multiple assay types from sample preparation to data generation. Responsible for experiments at the bench based on training and competencies can be assigned conduct, method development, validation and/or sample analysis. Can be assigned QC tasks. Execute appropriately method standard operating procedure (SOP), ensure completeness and accuracy of docume…

Organizational Development Lead

On-site · Laval

About The Role The Organizational Development Lead designs, leads, and implements organizational development initiatives and solutions that address business challenges, strengthen team and leadership effectiveness, and support organizational change. The role develops and maintains frameworks, tools, and processes for organizational design, succession planning, career development, talent assessment, and change management. Drawing on workforce data, employee feedback, and talent insights, the manager identifies improvement opportunities, evaluates initiative outcomes, and leads actions to enh…

Scientist, Pk & Biomarker

On-site · Laval

About The Role The Scientist, PK & Biomarkers is assigned to projects based on scientific competency and training. The Scientist will ensure the overall integrity/quality of assigned studies. The Scientist can also be designated as the main contact for client interactions laboratory for their assigned projects. What You'll Do Here Autonomous and proficient developing, planning, managing, conducting, reporting and troubleshooting multiple assay types to ensure scientific quality, regulatory expectations, and client satisfaction. Assigned by management on studies and tasks based on scientif…

Senior Workday ERP Analyst

On-site · Laval

About The Role The Senior Workday ERP Analyst is a functional and technical partner to the Altasciences Accounting and Finance teams. This role owns complex configuration, support, and continuous improvement across Workday Financials, Workday Adaptive Planning, Workday Payroll, and enterprise reporting. The analyst combines strong accounting knowledge with deep Workday expertise to translate business requirements into scalable solutions, reliable financial data, effective controls, and clear reporting.   The successful candidate will help lead major enhancements and cross-functional initiat…

Screening Quality Control Associate I

On-site · Montréal

The Screening Quality Control Associate I ensures the accuracy and compliance of clinical trial screening data by reviewing documentation and verifying participant eligibility. They also track data queries, identify error trends, and maintain enrollment logs while adhering to GCP and study protocols.

Facilities Maintenance Technician Level II

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.

Inventory Coordinator

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.