Clinical Scientist

Benefits include: Medical, Dental, and Vision Insurance, 401(k), Stock Options NOTE: You must have 5+ years experience in medical device, clinical research, data analysis, and medical writing with a strong preference for experience in the spine and/or implantable device industryto be considered for this position. Providence Medical Technology, Inc. is a privately-held medical device company focused on innovation solutions for cervical spine conditions. The company has pioneered a proprietary approach to posterior cervical fusion and has developed surgical instrumentation and implants that offer unique benefits to the $2 billion worldwide cervical spine market. Our purpose is to improve clinical outcomes for high-risk patients and prevent surgical failures of the cervical spine. LOCATION This is a remote position. SUMMARY As an integral team member of Clinical/Regulatory, the Clinical Affairs Scientist will serve a hybrid function spanning Medical Writing, Data Science, and Clinical Data Management. This role is designed for a small, agile clinical organization where cross-functional expertise is essential to maximizing the value of our clinical, bench, and real-world evidence datasets. The ideal candidate will help PMT deepen its understanding of our investigational and commercial product performance, identify pathways for future regulatory or marketing claims, support ongoing and new clinical studies, and lead the development of manuscripts, abstracts, and clinical documents that communicate our evidence to internal and external stakeholders. This position will play a critical strategic role in shaping PMT’s clinical evidence generation, data exploration, and scientific communications throughout the lifecycle of our cervical and lumber interventional spine technologies. MAIN RESPONSIBILITIES: Data Science & Evidence Exploration (~40%): Lead strategic analysis and exploration of PMT's clinical datasets to identify insights, claims opportunities, and research pathways. Conduct exploratory analyses on data from the IDE study, legacy clinical studies, real-world evidence programs, and materials/bench testing datasets. Integrate multiple datasets (IDE, post-market, legacy trials, bench data) to explore novel clinical or regulatory claims, identify signals, or highlight areas for further investigation. Develop analytical plans for exploratory work and hypothesis-generative analyses, independently and with consultation/guidance from team and PMT. Identify patterns or early signals that may support future studies, #J-18808-Ljbffr