Paige is a software company helping pathologists and clinicians make faster, more informed diagnostic and treatment decisions by mining decades of data from the world’s experts in cancer care. We are leading a digital transformation in pathology by leveraging advanced Artificial Intelligence (AI) technology to create value for the oncology clinical team.

We are the first company to develop clinical grade AI tools for the pathologist, which resulted in our receiving FDA breakthrough designation for our first product. Paige has also received FDA-clearance for our digital viewer, FullFocus™. We have also established multiple relationships with biopharma, laboratory, and equipment manufacturers that enables Paige to develop an ecosystem ready to help patients receive better diagnoses and treatment.

We are seeking an Director of Medical Affairs to join our team. In this role you will be responsible for all activities related to implementing our clinical and evidence development strategy. You will lead Paige’s relationship with clinical and health economic leaders, and guide our market access initiatives. This is a unique opportunity for a highly motivated individual that enjoys the challenge of commercializing next-generation technologies in the laboratory space.

At Paige we are working remotely until it is safe to return to the NYC office.  This position will be based in the NYC office once we return.  

As the Director of Medical Affairs you will:

• Own and execute the clinical evidence and access strategy for our clinical and biopharma products
• Work with KOLs to develop evidence supporting the commercialization of our products
• Design and lead in execution of clinical and health economic studies
• Lead market access initiatives, including obtaining reimbursement for our products
• Work with medical and patient organizations to influence adoption of Digital Pathology and AI in clinical practice and clinical guidance
• Work with product management and development teams to guide design of clinical and biopharma products
• Own and execute efforts to publish and present clinical evidence

About you:

• 15+ years’ experience in healthcare with a strong track record of generating the right evidence to drive market access
• Excellent 'c-suite' communication skills and experience with clinical studies
• Accountable, proactive, and thoughtful with demonstrated strategic problem-solving skills
• Ability to learn and understand disease, biology and technical concepts quickly
• Ability to manage multiple projects at the same time in a fast-paced environment
• Must be willing to travel up to 30%

Preferred:

• Strong knowledge of oncology, pathology, health economics and clinical studies
• Experience working in fast-paced start-ups
• Understanding of computer vision, machine learning and software as a medical device