Product Manager – Clinical & Evidence Strategy

🔥 3 hours ago

🧀 Wisconsin – Remote

🧀 Wisconsin – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

✅ Product Manager

👻 Ghost score 12%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Natus Medical Incorporated

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

🔧 Hardware

🏭 Manufacturing

💰 $30.8M Post-IPO Equity - Natus Medical on 2006-08

Healthcare • Hardware • Manufacturing

Natus Medical Incorporated is a medical device company that develops, manufactures, and distributes diagnostic and monitoring products for healthcare providers. Its offerings focus on neurological and neonatal care as well as hearing and balance assessment, including devices and associated software used in hospitals, clinics, and specialty practices. Natus primarily sells equipment and solutions to healthcare organizations worldwide.

📋 Description

• Define and support BrainWatch's clinical evidence strategy with Product Management, Clinical, and Regulatory teams • Identify evidence gaps required for adoption, reimbursement, and competitive differentiation • Support post-market clinical studies, data collection initiatives, and pilot programs • Translate clinical outputs into evaluation reports, publications, podium presentations, and marketing/product claims • Define clinically meaningful, evidence-backed product claims and maintain consistency across materials and studies • Define and validate target clinical use cases, including ICU monitoring, ED triage, and step-down settings • Map clinical workflows to identify adoption barriers, inefficiencies, and training gaps • Partner with Product Management and downstream teams to incorporate workflow needs into product design and field execution • Design and execute early adopter and lighthouse site programs with strategic customers • Validate workflows, generate real-world evidence, and refine scalable clinical use cases • Analyze competitor clinical evidence, claims, and study designs to identify differentiation opportunities • Establish processes to capture clinical feedback, workflow challenges, and outcome data • Translate insights into product inputs and prioritized evidence-generation opportunities • Support advisory boards, KOL engagement activities, and product feedback sessions • Collaborate with Marketing and Product teams to synthesize clinician insights • Support clinically accurate scientific presentations, study summaries, publications, and clinical use cases • Comply with Quality System procedures and regulatory requirements • Collaborate with Clinical Specialists, KOLs, Product Management, Marketing, Sales, Medical Education, Engineering, R&D, Quality, and Regulatory teams

🎯 Requirements

• Bachelor's degree in a clinical, scientific, or biomedical field (e.g., Neuroscience, Biomedical Engineering, Nursing, or Healthcare) required; advanced degree preferred • 3+ years of experience in clinical evidence strategy, medical affairs, clinical marketing, or product management in the healthcare/medical device industry • Demonstrated experience supporting post-market clinical studies, evidence generation, or clinical research programs • Proven experience in clinical evidence or product management within the medical device industry • Experience working with cross-functional, diverse teams in a multinational, dynamic organisation • Excellent analytical capabilities and experience gathering and interpreting clinical data and Voice of Customer (VOC) insights • Excellent communication abilities to articulate clinical value across stakeholders • Ability to lead cross-functional initiatives and influence without authority • Experience with regulatory compliance and clinical claims in the healthcare/medical device industry • Strong understanding of evidence requirements for adoption, reimbursement, and competitive differentiation • Compliance with relevant Quality System procedures and regulatory requirements • Reliable internet connection and ergonomically appropriate workspace • Quiet, distraction-free home office environment suitable for confidential work, frequent video and phone calls, and focused tasks

🏖️ Benefits

• Remote work arrangement • Hybrid arrangement available for candidates located near one of the company's office locations • Home office work environment • Limited travel to support team collaboration, business meetings, and key planning activities