Jobs at Altasciences

The Senior QA Auditor, GLP audits nonclinical and laboratory studies ensuring compliance with GLP regulations, maintains audit documentation, mentors staff, and interprets regulatory guidelines.

Manage end-to-end preparation and coordination of bioanalytical quotes: compile scientific and financial inputs, create and update proposals in CRM, manage change orders and version control, liaise with BD and Scientific Evaluators, maintain documentation, follow workflows, and drive process improvements.

Serve as single point of control for nonclinical studies: plan, coordinate, interpret, analyze, document and report results under GLP. Support protocol development, IACUC submissions, client interactions, QA audits, milestone tracking, and data archiving. Begin in training then assume Study Director duties with mentorship.

The Associate Scientist will assist the senior scientist in conducting scientific tasks, reviewing data, writing reports, and ensuring compliance with regulations in drug therapy development.

Lead and execute bioanalytical method development, validation, and sample analysis for preclinical and clinical studies. Ensure study quality and regulatory compliance (GLP/GCP/SOPs), manage projects, mentor analysts, troubleshoot assays, review data and deviations, and communicate results to clients and stakeholders.

The Scientist will manage and conduct method development, validation, and sample analysis studies while ensuring quality and compliance with regulations. They will mentor and support team members, interact with clients, and organize complex data reporting.

The Quality Control Coordinator ensures study and facility data are compliant with SOPs and GLP regulations, reviews protocols, maintains data quality, and communicates with team members to improve processes.

The Marketing Manager collaborates with internal teams to develop integrated marketing strategies, manage projects, and support brand awareness and lead generation for Preclinical services.

Assist senior scientist with bioanalytical tasks including data review, multi-batch trend analysis, report generation, method development/validation, sample analysis, documentation, inventory/order management, QA support, sponsor communication, and compliance with SOPs, GLP and GCP. Bilingual French/English communication required.

The Procurement Specialist I assists with supplier identification, purchase orders, and sourcing tasks, ensuring timely and compliant acquisition of materials and services.

The Senior Biostatistician leads statistical analysis in clinical trials, mentors other biostatisticians, and ensures high-quality deliverables according to regulatory standards.

The PK/ADA Scientist will manage analytical projects, ensure compliance, provide scientific guidance, and supervise laboratory staff while conducting method development and analysis in preclinical and clinical studies.

The IT Technical Support Supervisor manages IT Service Desk operations, ensures excellent customer service, provides technician training, and supports users with technology issues.

The Assistant, Study Operations provides administrative support for clinical trials, ensuring compliance with protocols and maintaining trial documentation and materials.

The Research Associate II will prepare dose formulations, ensure compliance with GLP, perform laboratory functions, and maintain supplies and cleanliness in the lab.

The Enterprise Procurement Specialist coordinates supplier contracts, sourcing initiatives, and cost-saving programs while ensuring contract compliance and operational efficiency.

The QC Reviewer is responsible for ensuring accurate batch documentation, performing quality control, mentoring analysts, and ensuring compliance with GLP and SOPs in the lab.

The Senior Lead Data Manager oversees data management activities throughout clinical studies, ensuring quality control, managing client relationships, and mentoring team members. Responsibilities include developing documentation, coordinating with database developers, and participating in process improvement initiatives.

As a Principal Research Scientist, you will lead technical expertise in LC-MS/MS, ensuring compliance with GLP, overseeing method validation, and training staff while interacting with clients and managing projects.