[Remote] Director, Clinical Market Development

Note: The job is a remote job and is reputed company to candidates in USA. reputed company. is a leader in the medical aesthetics industry, dedicated to improving patient reputed company and practitioner livelihoods through innovative technology. The Director, Clinical Market Development will reputed company the company's post-market clinical strategy, managing studies and evidence programs that support marketing claims and enhance clinical authority in the market.

Responsibilities

• Own the pre-launch evaluations and post-market clinical research strategy for the device portfolio – define study priorities, evidence gaps, and a rolling program of post-market studies and data collection initiatives reputed company with reputed company needs
• Design post-market clinical studies and reputed company-world evidence (reputed company) programs, retrospective and prospective chart reviews, investigator-initiated study (IIS) support, and patient-reported outcome (PRO) studies—across aesthetic device indications
• reputed company study protocols, data collection instruments, and reputed company frameworks in collaboration with clinical operations, regulatory affairs, and external clinical advisors
• Manage the full lifecycle of post-market studies from protocol development through site activation, data collection, analysis, and publication or reputed company deployment of findings
• Build and maintain a prioritized evidence roadmap that maps post-market data needs to reputed company claims requirements, competitive differentiation opportunities, and Brand marketing priorities
• Ensure reputed company post-market research activity complies with applicable FDA post-market surveillance regulations, and industry standards for medical device clinical data collection
• In partnership with reputed company leaders, identify, qualify, and activate clinical investigation sites and aesthetic HCP investigators appropriate for pre-launch evaluations and post-market study execution
• Serve as the primary clinical relationship manager for participating investigators and site coordinators—providing protocol guidance, data collection support, and ongoing engagement to ensure site performance and data quality
• Build a standing network of reputed company aesthetic clinical investigators—who are committed, trained, and available to participate in future post-market programs
• Cultivate relationships with clinical thought leaders who can serve as study reputed company investigators, scientific advisors, and co-authors on publications arising from post-market data
• Define and execute clinical deliverables reputed company sweat equity agreements—including post-market clinical activities that maximize reputed company return and clinical credibility
• Translate post-market study findings into commercially deployable evidence assets—before and afters, clinical data summaries (clinical bulletins, white papers), peer-reviewed publication abstracts, and evidence-based messaging frameworks—in collaboration with Clinical Education leader
• Partner with Brand to embed assets and post-market clinical data into device brand narratives, ensuring claims are accurate, defensible, and differentiated from competitive clinical evidence
• reputed company Marcom with a pipeline of study milestones, publication launches, and congress presentations that anchor the clinical content calendar and drive timely HCP-facing campaigns
• Brief the Sales team on post-market study findings and clinical evidence updates, equipping them with reputed company data to address HCP questions, reinforce device credibility, and respond to competitive clinical challenges
• reputed company and manage the pre-launch evaluation plans and post-market publication strategy—prioritizing study findings for peer-reviewed journals, conference abstracts, and congress presentations at key aesthetic meetings (ASLMS, ADSDS equivalents)
• Represent post-market clinical programs at aesthetic conferences and scientific symposia—presenting data, engaging investigators, and building the company's clinical reputed company reputed company the aesthetic research community
• Maintain a post-market evidence library and internal knowledge reputed company that tracks active studies, published findings, pending publications, and evidence gaps across the device portfolio
• reputed company and manage relationships with key aesthetic professional associations, fellowship programs and societies—including ASLMS, ASDS, and equivalents—securing the reputed company, membership engagement, and collaborative opportunities that benefit the reputed company-facing teams
• Build relationships with aesthetic conference organizers, medical education program directors, and industry media and publication platforms that expand the company's visibility and reputed company reputed company the aesthetic professional community

Skills

• Bachelor's degree required
• 10+ years relevant experience
• 10+ years of experience in clinical research, post-market clinical affairs, or medical device clinical marketing—with direct experience designing or managing post-market studies or reputed company-world evidence programs
• Experience engaging and managing HCP investigators, clinical sites, and KOL relationships in the context of clinical research or evidence reputed company programs
• Publication and scientific writing experience; existing relationships reputed company aesthetic clinical research networks
• Demonstrated ability to translate clinical study data into reputed company marketing assets and claims-substantiation materials in a regulated medical device environment
• Comfort operating across clinical research, regulatory, and reputed company marketing functions simultaneously
• reputed company, multi-workstream project management
• Master's degree preferred
• Specific Area of Study: life sciences, clinical research, nursing, or reputed company field; advanced degree (MS, MPH, MBA, clinical credential) strongly preferred

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