Clinical Evidence Scientist at Rivanna Medical, Inc.

Charlottesville, Virginia, United States -

Full Time

Start Date

Immediate

Expiry Date

07 May, 26

Salary

0.0

Posted On

06 Feb, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Data Analysis, Scientific Writing, Quantitative Analysis, Data Visualization, SQL, Clinical Databases, Stakeholder Communication, Project Management, Medical Device Experience, Site Performance Analytics, Grant Writing, AI Development Support, Evidence Generation, Publication Coordination, Statistical Methods, External Stakeholder Reporting

Industry

Medical Equipment Manufacturing

Description

Description Rivanna Medical, Inc. is seeking a Clinical Evidence Scientist to serve as the scientific owner of clinical data curation and analysis to support clinical evidence generation activities for the Accuro® 3S and Accuro® XV product lines. This role will translate clinical data into high-impact scientific outputs that directly support Limited Market Release commercialization/market access and external stakeholder needs, while informing clinical enrollment and site strategy decisions. This is a hands-on, multidisciplinary role working closely with Clinical Operations, R&D, and Commercial/BD to establish a reliable “evidence pipeline” of case studies, publications, whitepapers, and stakeholder-ready analyses. Responsibilities Execute clinical data organization and analysis activities for Accuro 3S and Accuro XV Generate claims-substantiating evidence assets for commercialization/market access, including: Case studies and evidence briefs Peer-reviewed manuscripts, abstracts, posters, and conference submissions Technical whitepapers / scientific content supporting product claims Maintain an evidence/publication plan, coordinate inputs from internal teams and external collaborators, and drive deliverables to submission. Support external stakeholder reporting through monthly evidence review decks and execution of ad-hoc analyses. Build and maintain site performance analyses to inform site initiation, optimization, and go/no-go gates. Leverage external datasets as needed to evaluate procedure-volume proxies and other market signals supporting value proposition development and future site targeting. AI-development support: deliver clinical stratification analyses and curated insights that support existing AI/model development owners. Contribute to grant or non-dilutive submissions when aligned with priorities and candidate experience. Requirements Education: PhD preferred in biomedical engineering, life sciences, clinical research, biostatistics, data science, or related field; MS with a strong publication/scientific writing record will be considered. Demonstrated experience analyzing clinical trial or clinical study datasets and translating findings into clear, defensible scientific conclusions. Strong track record of scientific writing (peer-reviewed publications, conference abstracts/posters, whitepapers). Grant-writing experience is a plus. Hands-on proficiency with quantitative analysis tools (e.g., Python and/or R, Excel; statistical methods; data visualization). SQL and experience with clinical databases/EDC tools (e.g., REDCap, Medrio, or similar) are a plus. Ability to create crisp, stakeholder-ready materials (slide decks, evidence summaries) and communicate across technical, clinical, and commercial audiences. Comfortable managing multiple priorities and stakeholders in a fast-paced, high-ownership environment. Preferred Qualifications Medical device experience (especially imaging, navigation, or ultrasound) and familiarity with clinical evidence expectations for commercialization. Experience supporting external stakeholders (government programs, strategic partners) with recurring reporting and rapid-turn analyses. Experience with site performance analytics and operational metrics in multi-site studies. About Rivanna Medical, Inc.: Rivanna Medical, Inc. is a privately held designer, manufacturer, and distributor of world-first, imaging-based medical solutions based in Charlottesville, VA. Rivanna Medical, Inc. operates an FDA-registered and ISO 13485:2016 certified manufacturing facility where it produces the Accuro® product line and related medical equipment and components. Accuro is the world's first spinal navigation device designed to improve the safety, speed, and efficiency of spinal needle guidance procedures. Rivanna Medical, Inc.'s revolutionary platforms feature BoneEnhance® Multi-Frequency Image Reconstruction, which optimizes ultrasound for the visualization of bony versus soft tissue anatomy, and SpineNav3D™ AI-Based Spine Recognition, which automates ultrasound image interpretation. Employee Benefits at Rivanna Medical, Inc.: Rivanna Medical, Inc. offers a comprehensive benefits package, which includes health insurance, vision and dental coverage, group life insurance, long-term disability insurance, paid time off, a 401(k) plan with company match, and more. We are continually seeking to enhance our team with individuals who bring unique perspectives and experiences. This diversity of thought and perspective drives innovation and strengthens our commitment to creating an inclusive team environment where our core values of trust, humility, and dedication are practiced every day. Equal Employment Opportunity Statement: Rivanna Medical, Inc. is committed to providing equal employment opportunities to all employees and applicants without regard to race, ethnicity, religion, color, sex (including childbirth, breastfeeding, and related medical conditions), gender, gender identity or expression, sexual orientation, national origin, ancestry, citizenship status, uniform service member and veteran status, marital status, pregnancy, age, protected medical condition, genetic information, disability, or any other protected status in accordance with all applicable federal, state, and local laws. All employees must be able to lift at least 25 pounds. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of their positions.

Responsibilities

The Clinical Evidence Scientist will execute clinical data organization and analysis activities to generate evidence assets for commercialization and market access. This role involves maintaining an evidence/publication plan and supporting external stakeholder reporting through analyses and presentations.