Kendra Hyland
Medical Writer and Clinical Scientist
- Role
- Clinical Product Risk Peripheral Interventions at Boston Scientific
- Location
- Minneapolis, MN, US
- LinkedIn followers
- 500 followers
About Kendra Hyland
Kendra has 19 years of medical writing experience, with over 7 years in the medical device industry experience. She is an experienced writer and project manager of medical devices for soft tissue surgery, medical device/drug combination products, and clinical studies. Kendra has authored or co-authored more than 45 clinical evaluation documents, summary of safety and clinical performance documents, periodic safety update reports as well as more than 20 manuals, 15 peer-reviewed manuscripts, abstracts, posters, and verbal presentations. Kendra is experienced with communicating complex information to diverse audiences and effectively collaborating cross-functionally with regulatory, project management, clinical, risk, human factors, legal, and marketing departments. Top Five Core Strengths from Clifton Strengths Finder1. Learner2. Input3. Analytical4. Responsibility5. Deliberative
Experience
Clinical Product Risk Peripheral Interventions
Feb 2024 — Present · Maple Grove, MN, US
Author of CEPs, CERs, PMCF-Plans, and PMCF Reports.• Contributor to creation and editing of SSCPs.• Knowledgeable about regulatory guidance relative to clinical evaluation, including EU MDR, EN ISO 14155, and MEDDEV.
Education
University of Minnesota-Twin Cities, College of Veterinary Medicine
Doctor of Philosophy (Ph.D.), Molecular Veterinary Biosciences (mucosal immunology)
1999 — 2004
University of the Pacific
Bachelor's Degree, Biology
1993 — 1997
Skills
- Microbiology
- Life Sciences
- Molecular Biology
- Technical Writing
- Publications
- Adobe Photoshop
- Genomics
- Technical Manuals
- Microsoft Office
- Grant Writing
- Scientific Writing
- Molecular Genetics
- Research
- Medical Devices
- Mammalian Cell Culture
- Biotechnology
- Technical Editing
- Vasont Content Management System
- Public Speaking
- Cell Biology
- Pre-Clinical Studies
- Real-Time Pcr
- Immunology
- Assay Development
- Newsletters
- Immunoassays
- Biochemistry
- U.s. Food and Drug Administration (Fda)
- Host-Pathogen Interactions
- Lifesciences
- Fda
- Dna Sequencing
- Real-Time Polymerase Chain Reaction (Qpcr)
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