Clinical Research

• Design and support real-world evidence studies, including research questions, endpoint definitions, analysis plans, data-quality review, interpretation, and results communication
• Develop study protocols and concepts for company-sponsored, collaborative, post-market, and pivotal studies
• Develop clinical evidence for regulatory briefing materials, submissions, and responses
• Drive study start-up and execution, including protocol and case-report-form development, vendor and investigator coordination, data review, issue resolution, analysis, and interpretation
• Partner with the CMO to identify evidence gaps and research priorities and drive an integrated evidence-generation plan
• Develop clinical evidence materials, competitive data comparisons, dossiers, evidence summaries, and scientific narratives
• Develop clinical and economic evidence summaries supporting reimbursement, payer engagements, and market-access activities
• Support scientific publications, abstracts, posters, congress presentations, and dissemination of clinical and real-world evidence
• Contribute to Medical Affairs strategy and evidence roadmap
• Support advisory boards, congress activities, medical education programs, and engagement with healthcare professionals, investigators, and key opinion leaders
• Participate in hazard analysis reviews, adverse-event and complaint evaluations, post-market safety activities, and related investigations
• Collaborate with the Chief Medical Officer, internal teams, external investigators, academic research organizations, analytics partners, and research vendors

Explore Associate Director, Clinical Research, Real-World Evidence at Sequel Med Tech. Review requirements and application details.