regulatory compliancesasclinical researchjmpbiostatisticsmedical devicesneurosurgeryclinical study designorthopedic surgery
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Обязанности чётко определены и связаны с клиническими исследованиями в MedTech, но работа только на месте и отсутствие конкретики о развитии могут повлиять на привлекательность вакансии.
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Понятные задачиВлияние на медицинуСамостоятельная роль
Оценка от Hirify AI
Мэтч & Сопровод
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Senior Clinical Scientist (MedTech): Developing clinical research strategies, study designs, protocols, and evidence communications for musculoskeletal and neuroscience medical technologies with an accent on clinical science, biostatistical analysis, and regulatory compliance. Focus on designing and interpreting clinical studies, translating results into scientific publications and presentations, and guiding pre-market and post-market evidence decisions.
Location: Audubon, PA, United States; travel up to 10% of the time
Company
hirify.global develops implants and enabling technologies that improve surgical techniques and outcomes for patients with musculoskeletal disorders.
What you will do
Develop clinical research strategies, identify evidence needs, and formulate research questions for musculoskeletal and neuroscience medical applications.
Design and evaluate clinical studies and document study protocols, tools, and methods.
Advise on study operations and interpret clinical research standards, regulations, scientific literature, and study data.
Analyze data using appropriate summary statistics and statistical tests.
Communicate study outcomes through conference presentations, peer-reviewed articles, graphical materials, and marketing communications.
Collaborate with Product Development, Marketing, Regulatory Affairs, investigators, advisors, and study teams to support evidence programs and decision-making.
Requirements
Typically, at least 5 years of related clinical and/or preclinical science experience with a Bachelor’s degree; or 3 years with a Master’s degree; or a PhD without experience; or equivalent work experience.
Strong analytical skills and experience with biostatistical analysis and related software packages such as SAS or JMP.
Excellent verbal and written communication skills.
Attention to detail, advanced critical-thinking and problem-solving skills.
Ability to lead research projects independently as a self-starter.
Proficiency with Microsoft Office products and data visualization and image production tools.
Ability to meet the physical requirements of the role, including sitting, climbing or balancing, stooping, kneeling, crouching or crawling, lifting or moving up to 10 pounds regularly and up to 25 pounds occasionally, and using close, distance, color, peripheral, and depth vision with the ability to adjust focus.
Nice to have
Previous publication history or contributions to peer-reviewed articles.
Culture & Benefits
Collaborative, scientifically rigorous environment focused on teamwork, innovation, customer focus, and results.
Work supports patient care improvements through advanced medical technology.
Commitment to ethical business practices, regulatory compliance, inclusion, and respectful collaboration.
Reasonable accommodations may be made for individuals with disabilities.
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