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Altasciences

Verified Job Source

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

Laval, Quebec

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

Screening Technician

Remote

Your New Company! At Altasciences we all move in unison to assist and work in the discovery, development, and manufacturing of new drug therapies to get them faster to people who need them. No matter your role, we all play an important part and you will have a significant impact on the health and well-being of people across the globe. By living our values of Employee Development, Customer Focus, Quality and Excellence, Respect and Integrity, we look to foster a passionate and collaborative work environment and we are looking for talented and enthusiastic people, like you, to join our growing…

Licensed Practical Nurse - Screening Department

On-site · Montréal

The Licensed Practical Nurse will screen clinical study participants by performing technical activities such as blood collection, safety measurements, and data collection. They are responsible for ensuring participant eligibility and compliance with study protocols, GCP, and SOPs.

Customer Service Representative

On-site · Montréal

The representative provides clinical trial information to volunteers and pre-screens them to determine eligibility. They are responsible for scheduling appointments and maintaining participant data in compliance with GCP and SOP standards.

Clinical Research Technician

On-site · Montréal

The Clinical Research Technician executes clinical trial activities, including sample handling and safety measurements, in compliance with study protocols and GCP. They are responsible for maintaining workstation cleanliness and ensuring the confidentiality of participants and sponsors.

Licensed Practical Nurse - Clinical Operations

On-site · Montréal

The Licensed Practical Nurse oversees the safety of clinical trial participants and maintains safety equipment in compliance with protocols and GCP. Key duties include performing safety assessments, blood collection, administering medication, and monitoring adverse events.