Jill Visor has been in the medical device industry for over 30 years focused on peripheral vascular, cardiovascular, gastroenterology, and neurology therapeutic areas. Her previous experience ranges across different spectrums of the industry including both in vitro diagnostic and implantable medical devices and roles as Vice President of Clinical and Regulatory Affairs for a medical device company and Director of Clinical Research Services at NAMSA.
Her notable highlights include collaborating with medical device companies to design and build accurate, efficient, and user-friendly databases leading to multiple product approvals. She initiated US and International clinical trials and coordinated all aspects of site management and monitoring, and managed multidisciplinary product development team activities including adherence to timelines, meeting conduct, conflict resolution, and strategic communication.
Jill has her Masters in Pharmaceutical Chemistry from the University of Florida.
CORE COMPETENCIES
- Proficient in design, development, and validation of iMedNet, Merative Zelta, and iMedidata RAVE databases
- Clinical and data management expertise in protocol review and CRF/database optimization for endpoint capture and usability
- Experienced in building and implementing database features including randomization, inventory management, ePRO/eCOA, econsent, coding, payment, batch upload and report creation
RECENT PROJECTS
- Database design, development, management in the following therapeutic areas:
- Heart failure treatment for functional mitral regurgitation
- Heart failure management system
- Neuromodulation for chronic pain
- Neuromodulation for Rheumatoid Arthritis
- Hydrogel spacers for prostate cancer therapy
- Hemostatic agent for GI bleed
- Hemostatic agent for femoral arteriotomies
- Heart Lung machine
- Sleep apnea prevention device
- Ophthalmic measurement systems
