Jobs at Altasciences

Lead immunogenicity (ligand-binding) assay development, validation, and sample analysis for clinical and nonclinical studies; act as client-facing Bioanalytical PI, mentor analysts, troubleshoot assays, report results, and ensure compliance with GCP/GLP/SOPs.

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.

Manage full-cycle recruitment for entry-level, technical, scientific, high-volume and professional roles. Partner with hiring managers on sourcing strategies, candidate assessment, and timely hiring. Maintain ATS data, build talent pipelines, support employer branding, track recruiting metrics, ensure compliance, and drive recruitment process improvements.

Drive prospecting and lead qualification for Altasciences by researching accounts, generating interest, following up on inbound leads, managing outreach campaigns, documenting activity in Salesforce/CRM, and routing qualified opportunities to sales directors. Produce KPI reports, support business travel and conference outreach, and collaborate with Marketing and BD to expand the prospect database.

Perform bench laboratory work using LCMS methods, execute SOPs, and complete accurate GLP/GCP documentation. Conduct sample analysis or validations per training, communicate quality or data concerns, follow health and safety standards, and maintain up-to-date procedural knowledge.

Perform bench work and documentation for ligand binding and other assays, including method development, validation, sample analysis, QC tasks, and adherence to SOPs, GLP/GCP. Mentor junior analysts, ensure data integrity, maintain safety standards, and communicate issues to management. Bilingual French/English communication required.

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.

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.

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.

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.

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.

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.