Product Manager – Clinical & Evidence Strategy

Posted Sep 16

This is a fully remote position, open to applicants in Wisconsin.

📋 Description

• Develop and enhance BrainWatch's strategy for clinical evidence in collaboration with Product Management, Clinical, and Regulatory teams.

• Identify gaps in evidence necessary for adoption, reimbursement, and competitive advantage.

• Assist with post-market clinical studies, initiatives for data collection, and pilot programs.

• Convert clinical results into evaluation reports, publications, presentations, and marketing/product claims.

• Establish clinically relevant, evidence-supported product claims and ensure consistency across all materials and studies.

• Define and validate target clinical use cases, including ICU monitoring, emergency department triage, and step-down care settings.

• Analyze clinical workflows to pinpoint barriers to adoption, inefficiencies, and training needs.

• Collaborate with Product Management and downstream teams to integrate workflow requirements into product design and implementation.

• Design and implement early adopter and lighthouse site programs with strategic customers.

• Validate workflows, produce real-world evidence, and enhance scalable clinical use cases.

• Evaluate competitor clinical evidence, claims, and study designs to find opportunities for differentiation.

• Set up processes to capture clinical feedback, workflow challenges, and outcome data.

• Transform insights into product inputs and prioritize opportunities for evidence generation.

• Aid in advisory boards, KOL engagement initiatives, and product feedback sessions.

• Work with Marketing and Product teams to consolidate clinician insights.

• Assist in creating clinically accurate scientific presentations, study summaries, publications, and clinical use cases.

• Adhere to Quality System procedures and regulatory standards.

• Collaborate with Clinical Specialists, KOLs, Product Management, Marketing, Sales, Medical Education, Engineering, R&D, Quality, and Regulatory teams.


⛳️ Requirements

• A bachelor's degree in a clinical, scientific, or biomedical discipline (e.g., Neuroscience, Biomedical Engineering, Nursing, or Healthcare) is required; an advanced degree is preferred.

• Over 3 years of experience in clinical evidence strategy, medical affairs, clinical marketing, or product management within the healthcare/medical device sector.

• Proven experience in supporting post-market clinical studies, evidence generation, or clinical research initiatives.

• Established background in clinical evidence or product management in the medical device industry.

• Experience collaborating with cross-functional, diverse teams in a multinational and dynamic environment.

• Strong analytical skills and experience in gathering and interpreting clinical data and Voice of Customer (VOC) insights.

• Exceptional communication skills to effectively convey clinical value to various stakeholders.

• Ability to lead cross-functional projects and influence without direct authority.

• Familiarity with regulatory compliance and clinical claims in the healthcare/medical device sector.

• Comprehensive understanding of the evidence requirements for adoption, reimbursement, and competitive differentiation.

• Compliance with applicable Quality System procedures and regulatory standards.

• Reliable internet connection and an ergonomically suitable workspace.

• A quiet, distraction-free home office environment conducive to confidential work, frequent video and phone calls, and focused tasks.


🏝️ Benefits

• Opportunity for remote work.

• Hybrid work arrangements available for candidates near one of the company's office locations.

• Home office work environment provided.

• Minimal travel required to facilitate team collaboration, business meetings, and key planning activities.

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