Jobs at Altasciences

Coordinates end-to-end clinical trial execution from study award through archival. Responsibilities include maintaining timelines, tracking risks and issues, coordinating stakeholders, supporting meetings and regulatory submissions, maintaining inspection-ready Trial Master File documentation, coordinating vendors and sites, supporting GxP compliance, and tracking training records. The role requires strong communication, organization, judgment, confidentiality, prioritization, and the ability to manage competing activities independently.

Develops proactive talent attraction and sourcing strategies across North America. Responsibilities include passive candidate engagement, talent pipeline and community development, full-cycle recruitment, employer branding, recruitment marketing, university partnerships, candidate experience, and talent analytics. The role manages requisitions from intake through offer acceptance, partners with hiring managers and marketing, supports scientific and technical hiring, and uses sourcing metrics and market intelligence to improve recruitment outcomes.

Coordinates marketing activities to recruit clinical trial participants, including newsletters, social media, paid advertising, geofencing, landing pages, SEO, community engagement, and participant communications. Tracks recruitment KPIs, budgets, billing, referrals, invoices, translations, and advertising approvals. Prepares IRB packages, manages vendors, supports marketing events, and ensures compliance with study protocols, GCP, SOPs, confidentiality, and brand standards.

Serve as Workday HCM SME for Time Tracking and Absence modules: configure and maintain business processes, reports, validations, security and calculated fields; translate HR requirements into scalable Workday solutions; manage change intake, testing, releases, and data governance; build dashboards, support audits, and identify process improvements to ensure data quality and user experience.

The Biostatistician II independently leads clinical and preclinical study analyses, develops randomization schedules, statistical analysis plans, tables, figures, listings, and SAS programs. The role performs quality control, supports regulatory responses, reviews protocols and statistical reports, coordinates with clients and multidisciplinary teams, and ensures compliance with SOPs, GCP, ICH, FDA, EMA, and other regulatory guidelines.

Support senior scientists in bioanalytical studies: perform data review, assay development/validation bench work, draft reports and SOPs, schedule analyses, manage reagents/inventory, respond to QA, and ensure GLP/GCP compliance.

Perform quality control of laboratory data and batch documentation per SOPs and GLP. Review and compile study documents, report results, monitor lab quality, mentor analysts, support inspections, and assist scheduling and instrument verification as assigned.

Performs laboratory quality control reviews for bioanalytical batches, documentation, procedures, instrumentation, and analyst practices. Ensures compliance with GLP, SOPs, and regulatory requirements; identifies trends, deviations, and nonconformities; supports inspections and quality assurance responses; supervises documentation processes; drafts study documents and reports; and helps coordinate sample analysis deadlines. Requires a relevant science degree, pharmaceutical or medical experience, strong technical writing and communication skills, proficiency with Microsoft Office, and English-language protocol comprehension.

Supports bioanalytical services compliance by writing and revising SOPs, templates, validation plans, and reports. Prepares responses to clients, regulators, audits, and deficiency letters; supports quality management initiatives; monitors regulatory developments; and presents departmental trend reports. Performs all work according to SOPs, GLPs, GCLPs, regulatory guidelines, and company policies.

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.

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.

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.