Scientific Director – Breast Cancer Portfolio

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Artera.net

WebsiteLinkedInAll Job Openings

11 - 50 employees

Founded 2002

💼 Consulting

📦 Logistics

📣 Marketing

Consulting • Logistics • Marketing

Artera. net is a leader in providing B2A (Business to Agency) solutions, specializing in premium hosting and cloud services tailored for agencies and their digital needs. The company offers a comprehensive array of services including hosting, cloud server, and cloud enterprise solutions. Artera. net emphasizes innovation, reliability, and security, boasting high-quality infrastructure with proprietary data centers in Switzerland, robust anti-DDoS protection, and compliance with privacy regulations including GDPR. Their offerings include pro-active 24/7 support with direct communication with system experts, ensuring high levels of customer satisfaction with a renewal rate of 93%. Artera. net also promotes environmental sustainability by powering its data centers with renewable energy. With a partnership program for web companies, software houses, and freelancers, Artera. net aims to build long-term, trust-based relationships while offering customized and flexible technology solutions that cater specifically to the needs of each project.

📋 Description

• Provide scientific and strategic leadership for evidence generation across the breast cancer diagnostic product portfolio • Develop and execute integrated evidence-generation strategies for in-development and commercially available assays • Define evidence requirements for product development, regulatory submissions, reimbursement, clinical adoption, and guideline inclusion • Identify opportunities for indication expansion and next-generation product development • Partner with stakeholders to identify, evaluate, and prioritize clinical datasets • Provide scientific oversight of retrospective, prospective, observational, and translational studies • Develop study concepts, research plans, protocols, and endpoints with Biostatistics and Medical • Oversee study execution, interpretation, reporting, progress, and scientific or operational challenges • Establish and maintain relationships with key opinion leaders, academic medical centers, cooperative groups, and research networks • Lead external scientific collaborations and serve as the primary scientific contact for investigators • Author and review research proposals and evaluate external proposals • Develop publication strategies and lead abstracts, presentations, posters, and peer-reviewed manuscripts • Translate study findings into rigorous, clinically meaningful evidence and present scientific data • Partner with Product, Medical, Biostatistics, AI, and Market Access teams • Represent Clinical Development on cross-functional product teams and contribute to product claims, target product profiles, and commercialization strategies

🎯 Requirements

• Ph.D., M.D., Pharm.D., or equivalent advanced degree in oncology, cancer biology, pathology, molecular biology, epidemiology, or a related discipline • Minimum of 5 years of experience in oncology clinical development, translational research, diagnostics, biotechnology, or pharmaceutical development • Demonstrated expertise in breast cancer biology and clinical management • Experience developing and executing clinical studies supporting molecular diagnostics, digital pathology, genomic assays, AI-based diagnostics, or companion diagnostics • Experience leading collaborations with academic investigators and cooperative research groups • Track record of first-author, senior-author, or collaborative peer-reviewed publications • Experience authoring study protocols, research proposals, abstracts, and manuscripts • Strong understanding of clinical trial methodology, observational studies, and translational research • Experience working in cross-functional environments involving regulatory, product, commercial, and scientific stakeholders • Excellent communication, presentation, and relationship-building skills, with the ability to engage clinical experts • Strong strategic thinking and analytical skills • Comfortable operating independently in a fast-paced, collaborative startup environment with a high degree of ownership • Passion for improving patient care through AI-driven healthcare innovation • Expected travel up to 5% domestically and internationally for scientific collaboration meetings • Preferred: experience developing evidence strategies for commercially available diagnostic assays • Preferred: experience supporting regulatory submissions for diagnostic products • Preferred: familiarity with breast cancer prognostic, predictive, and treatment-selection assays • Preferred: experience with real-world data, real-world evidence, and outcomes research • Preferred: knowledge of digital pathology, artificial intelligence, machine learning, or multimodal biomarkers • Preferred: existing relationships with breast cancer investigators, cooperative groups, and academic research networks

🏖️ Benefits

• Equity is a core component of compensation • 401k matching • Unlimited paid time off (PTO)