Senior Clinical Evidence Specialist

Description:

The Senior Clinical Evidence Specialist supports the development, evaluation, and communication of clinical evidence for Neuromodulation therapies. This role partners with physicians and cross-functional stakeholders to advance scientific publications, assess evidence gaps, support evidence strategies, and ensure the accuracy and quality of clinical and scientific communications.

Primary Responsibilities
 

• Develop, author, and submit scientific manuscripts, abstracts, posters, podium presentations, and clinical evidence reports.
• Conduct literature reviews and synthesize scientific data to support evidence generation, publication activities, and business objectives.
• Lead or support medical evidence assessments and evidence gap analyses to inform clinical and evidence strategies.
• Collaborate with physicians, investigators, and healthcare professionals on publication development and scientific communications.
• Partner with Marketing, Medical Affairs, Reimbursement, Regulatory Affairs, Research and Development, and Clinical teams to provide clinical evidence expertise.
• Review clinical and scientific content for accuracy, including marketing and educational materials.
• Support investigator meetings, advisory boards, and external research collaborations.
• Maintain publication and literature databases and support responses to regulatory, audit, or submission-related inquiries.
  
   

Required Qualifications
 

• Bachelor's degree with 4+ years of experience in clinical research, scientific publications, clinical studies, or program management OR advanced degree with 2+ years of experience in clinical research, scientific publications, clinical studies, or program management.
• Experience authoring or contributing to scientific manuscripts, abstracts, clinical reports, or evidence-based communications.
• Experience conducting literature reviews, evidence assessments, or scientific data analyses.
• Experience collaborating with cross-functional stakeholders in a matrixed environment.
• Experience supporting regulated clinical research activities within the medical device, pharmaceutical, biologic, or healthcare industry.