Profile Summary
Ph.D. level scientist with more than 18 years of experience in both academia and industry. Experience in multinational corporations, managing d...
I am an agile, performance-driven and critical problem solver scientist with a passion for scientific, pharmaceutical, medical devices, and str...
I did a PhD in Biochemistry and worked in biomedical research for the past 15 years. I have extensive experience in clinical research, scientif...
I am a multi-disciplinary researcher with more than 20 research publications in peer-reviewed journals and over 10 years of experience in resea...
Broad hands-on software and hardware development for medical devices such as diagnostic imaging devices (PET, MRI, X-Ray and Ultrasound), blood...
I provide clinical research and health consulting, medical writing and training services to Pharma, Biotechnology Companies, CROs, NGOs, Founda...
CV • Progressed from fundamental multidisciplinary research (Chemistry, Nanobiotech, Biochemistry) to in vitro Pharmacology (Cell Biology, Targ...
Dr. William McGill is a researcher and biostatistician with wide-ranging experience in the health care and wellness industry. William has signi...
Ph.D. in biomaterials with an innovative and entrepreneurial mindset. My expertise includes project design and management, biomaterials design,...
Regulatory technical writer with experiences in the medical device, pharmaceutical, and cosmetic industries. Demonstrate extensive knowledge in...
Over 5 years’ experience in Quality and Regulatory Affairs, and technical submissions for a range of medical devices, including Orthopaedics, S...
An accomplished, versatile, results-oriented clinical research professional with over 14 years of experience in the Pharmaceuticals & M...
A seasoned professional with a decade of experience, I am a Leader and Speaker in the field of Quality Assurance & Regulatory Affairs, ...
PhD, postdoc, senior researcher in medical physics, imaging, radiotherapy. Extraction of attributes from real-world collected data. Medical Im...
Over 15 years of experience in the life sciences industry from R&D chemist, to drafting and prosecuting chemical, biochemical, and mate...
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• Medical Doctor (family physician); PhD and MSc (Neurology), Business (MBA) and (PMP )project management courses • Director of Business Develo...
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PhD Clinical Scientist with 10+ years experience in clinical diagnostic testing, biomarkers, clinical research, pathology and laboratory medici...
• Versatile Ph.D. medical writer. Have written medical manuscripts on a wide variety of topics, including clinical trials, drugs, and medical d...
I have over 8 years of experience in Clinical Research, Regulatory Affairs and Quality Assurance of implantable and electro medical devices in ...
I am a specialist medical writer providing...expertise in planning, researching and writing high quality systematic and scoping review articles for publication...
Mark Luhovy, MD is a medical doctor and biomedical engineer who has dedicated 20 years to the pursuit of understanding the intersection of medi...
Bio-pharma & Medical Device Quality Consultant having a good blend of Manufacturing, Technology & Business with in-dept...
MDR and MDD Gap assessments and Remediation. Risk documents creation and all remediation process knowledge to get the CE mark for the product t...
Career Profile Regulatory Affairs Specialist with 5+ years of experience, in the creation and compilation of regulatory submissions to regulato...
Medical technology and medical education marketing consultant and PR specialist, specializing in the cardiovascular field. Also, published jour...
Hire top medical device engineering consultants for help with FDA approvals, 510(k) submissions, EU MDR compliance and more. Get end-to-end product development support. Work with medical device engineering consulting experts for help with content writing and medical copywriting.
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Cost consequence analysis modeling for medical device$1000.00
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Freelance regulatory affairs consultant$1500.00
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CER Writer for Class I medical device$2000.00
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Literature review for medical device$2000.00
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FDA Submission for PPE$5000.00
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FDA DHF revision$3500.00
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Medical device engineering consultants for hire$1000.00
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A medical device consultant works with medtech companies to help them develop and design products, meet regulatory requirements, conduct clinical trials and market the product. A medical device expert can have 10-20 years of experience in the field in the areas of compliance and product design. A medical device writer can help with regulatory documents such as FDA submissions, Clinical Evaluation Reports, clinical trial protocols, and grants, as well as with content writing requirements such as white papers, blog articles and press releases. Companies worldwide are increasingly seeking medical device expertise on demand as it allows the flexibility of hiring remote workers as and when required.
Medical device companies have typically used a medical device consultancy to outsource their tasks. However the freelance revolution has made it possible for them to hire experts for short-term or contract projects. Hiring experts directly requires no minimum commitment or contract. A medical device engineering consultant freelancer can provide a variety of services ranging from literature search and systematic reviews to statistical analysis and clinical research. On Kolabtree, it's quick and easy to directly contact a freelancer and have one-to-one conversations about your requirements.
A medical device writing expert can provide a wide range of services that help medtech SMBs save precious time and energy. These include but are not limited to:
-Developing 510(k) submissions for FDA approval
-Developing CERs, clinical research protocols, and clinical case studies
-Putting together grant applications and proposals
-Writing and reviewing blog articles, website content, white papers and ebooks
-Writing and editing research papers and preparing them for journal publication
Working with a medical device writing consultant is becoming an increasingly popular choice among medtech businesses so that they can streamline their resources. With scientists and industry experts working remotely, it's possible to access medical device expertise in domains like cardiology, orthopedics, medical imaging, and more.
From ideation to product marketing, medical device engineering consultants can work with you at every stage of the product cycle. A medical equipment consultant can improve and optimize the design of equipment such as MRIs, ultrasound machines, etc. Biomedical engineers can work on a contract basis to provide prototypes and the final product design. A medical device marketing freelancer can develop creative campaigns and brand messaging to position your product in the market. A medical device development freelancer is typically an experienced expert, who can help with validation, verification, testing and compliance of the product. Medical writing is one major function that can easily be outsourced to qualified experts: a medical device writing freelancer can develop compelling, authoritative copy for your target audience.
The hourly rate for hiring medical writers on Kolabtree is $40 to $70. The fee for your project will depend on the expertise required, how urgently the work is needed, and what level of speciality you're looking for. Medical device consultants who work on design, development and compliance can charge up to $300 per hour. On Kolabtree, you can discuss your requirements directly with experts and get a range of quotes before choosing the best expert based on your budget and timeline.
