Jobs at Altasciences

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.

Provide administrative and professional support to Study Directors and PIs for GLP and non-GLP studies: prepare and manage protocols and study materials, schedule data collection, review raw data for errors and GLP compliance, coordinate audits and client visits, perform data verification, generate data tables, assist report drafting and archiving, and track study milestones.

Perform independent audits of clinical and laboratory study activities and documents to ensure compliance with protocol, SOPs, GxP, and regulations. Report findings, write inspection reports, evaluate responses, support vendor/equipment/software validations, maintain QA records, identify process improvements, and prepare for RQAP certification under mentor supervision.

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

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.

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.

Review and validate screening-phase clinical trial data for protocol, GCP, and SOP compliance; track and resolve data queries; verify participant eligibility; report trends, deviations, and complete documentation; assist screening activities and communicate issues to management.

Develop and validate LC-MS/MS assays, perform precise bioanalytical sample analysis for preclinical/clinical studies under GLP, manage project timelines, collaborate with clients, validate methods, and supervise laboratory staff.

Generate and manage client and vendor contracts (SOWs, TOROs, MSAs, CDAs, amendments, change orders). Track contracting timelines, maintain contract documentation in the CRM, support internal teams on contract changes, and participate in process improvements to ensure timely, accurate contract delivery for clinical projects.

Administer and maintain the MasterControl quality management system to support GxP compliance. Provide system administration, issue management with the vendor, application updates, user support and training, documentation/version control, and audit/inspection subject-matter expertise. Collaborate with QA and IT, prioritize and manage workloads, and identify continuous improvement opportunities to enhance compliance and operational efficiency.

Provide administrative support to the Proposals Team: monitor inboxes, manage SalesForce change orders, track proposal data, generate reports, attend meetings and take notes, assist with delays/cancellations, and recommend process improvements while maintaining confidentiality.

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.

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

10-week internship conducting user research to prototype AI-assisted report drafting. Interview report authors, map authoring workflows, define trust criteria for AI-generated drafts, sketch reviewer interactions, collaborate with engineering interns, and produce a working prototype plus a recommendation.

Intern team will build fast prototypes using LLMs and OCR to auto-populate scientific reports. Work includes wiring APIs, handling real document content, user interviews with report authors, pair-programming, and delivering a working prototype plus recommendations.

10-week internship building an AI-powered prototype to auto-populate report drafts. Run interviews with report authors, translate fuzzy problems into scoped deliverables, manage the team's plan and communications, guide engineering interns, and co-author a final recommendation on feasibility and next steps.

Lead enterprise site partnership strategy and manage executive relationships with investigative sites to improve start‑up, enrollment, contracting efficiency, and study delivery. Oversee site tiers, performance metrics, contracting, onboarding high‑performing sites, cross‑functional issue escalation, and integration of site insights into protocol design and operational planning. Represent the organization externally and report site trends to senior leadership.