Antara Mazumdar

• • Commercial & Strategic Alignment: Accountable for driving key projects across Product Strategy, Marketing, and Clinical Affairs to enable the commercial growth of the Focal One platform.

• • NHS Business Case Development: Spearheaded the development of clinical and economic business cases for the NHS (UK), aligning Real-World Evidence (RWE) and cost-benefit analysis to secure executive-level buy-in for focal therapy adoption.

• • Workflow Optimization & Market Adoption: Led cross-functional teams to optimize clinical workflows, directly facilitating medical education efficiency and standardizing international market adoption.

• • Central Information Reference (Congress & Market): Managed execution efficiency for international medical congresses, ensuring product positioning and messaging are streamlined across diverse technical and commercial stakeholders.

• • Clinical Affairs & Compliance Coordination: Support the planning and tracking of Clinical Affairs activities through structured project management plans, ensuring all activities align with Ethics, Quality, and CE-Mark regulatory requirements.

• • Clinical Registry Planning: Coordinate clinical registry initiatives (including exploratory pathways) to generate the data required for future clinical evaluation and strategic market positioning.

• • Strategic Partnership Leadership: Served as the primary external lead for multi-million-euro collaborations with global pharmaceutical leaders (AstraZeneca, Exact Sciences, NSABP), ensuring project coherence and strategic alignment across international borders.

• • Global Project Deployment: Directed product rollouts and clinical integrations across a prestigious network of international institutions (McGill, IEO Milan, NHS), managing key milestones and identifying friction points to optimize execution.

• • Cross-Functional Project Lifecycle: Managed the end-to-end execution of specialized AI portfolios (gBRCA Genomic Prediction & RlapseRisk), coordinating R&D, Clinical, and Technical teams to calculate recurrence risk and genomic mutations.

• • Operational Excellence & Compliance (ISO 13485 / IVDR): Authored and maintained "Audit-Ready" documentation for the legal and technical "Go-Live" of Medical Devices, ensuring strict adherence to ethical and regulatory procedures.

• • Supplier & Technical Operations: Managed technical infrastructure audits and deployment assessments; coordinated with Site Reliability Engineering (SRE) and external contractors to resolve integration bottlenecks and latency issues.

• • Change Management & Standardization: Developed and delivered specialized training for clinical leads and pathologists, ensuring standardization of data inputs and driving the clinical adoption of CE-marked diagnostics.

• • Information Consolidation & Reporting: Utilized advanced project tools (Jira, Notion, Zendesk) to consolidate information flows, adapt communication for diverse stakeholders, and report on strategic KPIs.

Moved from early-stage radiology AI environments to established French medtech companies for large-scale precision oncology projects.

• • Global Vendor & Portfolio Coordination: Accountable for a strategic portfolio of 10+ global AI partners (e.g., Lunit, Qure.ai), ensuring project coherence and alignment with clinical workflow requirements across the UK and EU.