Tango Vision Consulting
Clinical & Scientific Affairs Consulting
Helping MedTech & Biotech companies with 23 years of hands-on experience.

Clinical & Scientific Affairs Consulting
Helping MedTech & Biotech companies with 23 years of hands-on experience.

Andrea Scicli, Ph.D. is a Clinical and Scientific Affairs consultant with 23+ years of experience in
MedTech and Biotech, specializing in regulatory submissions, global clinical trial management, and
scientific communications for Class II and III medical devices.
She holds a PhD in Neurobiology from the University of Southern California and has authored 15+
peer-reviewed publications and abstracts presented at AHA, TCT, ACC, ESC, ISC, and CRT. Her
therapeutic expertise spans neurovascular devices, renal denervation, spinal ablation, vertebral
compression fractures, carotid and peripheral vascular disease, and ophthalmology.
As founder of Tango Vision Consulting, Andrea partners with MedTech startups and global
organizations to deliver tailored solutions in clinical trial management, regulatory strategy (IDE, PMA,
Breakthrough Device), medical writing, and scientific affairs. Prior corporate experience includes
Recor Medical, Stryker Neurovascular, DFINE, Abbott Vascular, Boston Scientific, and Medtronic.
Having worked across continents and speaking Spanish, Andrea brings a unique global perspective
to clinical and scientific affairs, enabling effective collaboration with diverse international teams and
clients
Contact via email at andrea@tangovisionconsulting.com or schedule a call (see link below) to discuss potential collaborations.
Driving healthcare advancements with tailored, transparent solutions in clinical and scientific affairs, providing innovative strategies to enhance patient outcomes through expert collaboration.
Tailored medical writing services that transform complex scientific data into clear and compelling narratives for regulatory approval and publication, effectively conveying your research findings to diverse stakeholders
Develop and organize advisory board content, manage key opinion leader participation and contracts, provide logistical assistance, and execute advisory boards
Create and implement effective training programs that drive excellence and continuous improvement in organizations and medical education content for training healthcare professionals
Support organizations in navigating the grant lifecycle, from application to project completion, ensuring compliance and success
Clinical trial management services that enhance the management and execution of clinical trials, optimizing operations to ensure compliance, efficiency, and successful trial execution
IDE, PMA, and Breakthrough Device submissions; risk management files; design control documentation; SOP development
Expert medical writing for clinical study reports, regulatory submissions, publications, abstracts, and grant proposals
Protocol development, registry start-up and management, post-market evidence strategies
Electronic data capture system design, CRF development, database build and implementation
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