Kerry Arnold

Senior Market Development Manager

Role: Senior Market Development Manager at Intrinsic Therapeutics, Inc
Location: Jacksonville, FL, US
LinkedIn followers: 500 followers

Sales & Business DevelopmentView LinkedIn profile

About Kerry Arnold

RN, BSN passionate about helping people gain access to exceptional care and products-Over 17 years in healthcare and medical device industries with management experience-Recently specializing in working with neurosurgeons and orthopedic surgeons for a treatment alternative to a spinal fusion-Experienced professional educating office staff regarding the authorization process, appeal process, billing, coding to help more patients gain access to care-Facilitate community education programs-Proficient Operating Room Nurse in Spine Surgery, Neuro Surgery, Urology, ENT, GI and General Surgery-Adept computer skills- Excellent interpersonal and communication skills-Proven track record meeting and exceeding goals and objectives-Motivated team player -Established trusted professional relationships-Deliver outstanding support and customer service with trusted relationships to physicians and customers

Experience

Senior Market Development Manager
Intrinsic Therapeutics, Inc
May 2023 — Present

Education

Florida State College at Jacksonville
Associate of Science (A.S.), Registered Nursing/Registered Nurse
1998 — 2002
Chamberlain University
Bachelor of Science (BS), Registered Nursing/Registered Nurse
2013 — 2014

Skills

Strategic Planning
Orthopedic
Medicine
Healthcare Management
Urology
Neurosurgery
General Surgery
Pediatric Urology
Nursing
Triage
Healthcare
Patient Safety
Spine
Pediatric Ophthalmology
Surgery
Sinus Surgery
Pediatrics
Plastic Surgery
Gastrointestinal Surgery
Ent
Pediatric Surgery
Orthopedics

Contact information

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Work email
k••••••@barricaid.com
Personal email
•••••@•••••.com
Direct dial
+19•••••••28

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Current company

Intrinsic Therapeutics, Inc

Medical Equipment Manufacturing · 91 employees · Founded 2000 · Woburn, Massachusetts, United States

Adjacent to a lumbar discectomy, the Barricaid® device is designed to close large defects in the annulus, which often lead to disc reherniation and/or disc collapse. Barricaid is a permanent implant with two components - a titanium bone anchor and a flexible polymer barrier. The barrier is designed to prevent reherniation by physically blocking the annulus at the post-surgery defect. The anchor component is comprised of titanium alloy that is placed into either the caudal or cranial-adjacent vertebral body to secure the device in position. The Barricaid has been studied in a definitive – level 1B evidence - randomized superiority trial with over 550 patients enrolled (clinicaltrials.gov NCT01••••38). The study focuses on patient at highest risk of reherniation and reoperation, enrolling only those patients with large defects (width >5 mm). The co-primary endpoints of reherniation and an 8-point composite of safety and effectiveness are evaluated at 2 years, with a parallel cost effectiveness analysis. Treated patients were found superior on both endpoints, with significantly lower rates of symptomatic recurrences (12% vs. 25%, p<0.001), index-level reoperations (9% vs. 16%, p=0.01), and device or procedure related serious adverse events (SAEs)(7% vs. 17%, p=0.001). Through two years, a total of 29 reoperations were performed in Barricaid subjects in comparison to 61 procedures in Controls. Study results are published in The Spine Journal, May 2018. Barricaid is FDA-Approved For full risk/benefit, see:

barricaid.com

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