Profile Summary
I have 3 years of research experience in writing scientific contents i.e research articles, Synopsis, thesis/dissertation etc. I have completed...
My science qualification is Ph.D. in pharmaceutical science. My writing qualifications: - Writing in the Sciences Certificate (Stanford Univers...
I am a process and product development commercialization consultant and project manager with an automation and mechanical engineering backgroun...
I am the holder of highly prestigious Tier 1 Exceptional Talent Visa and endorsed as such by the Royal Academy of Engineering in the fields of ...
Scientific Writer with 10+ years of experience with a demonstrated history of working in the Medical Device domain, SME in Clinical Evaluations...
An experienced clinical research and medical device Technical file writer who has certified on MEDDEV 2.7/1 Rev#4 documentation, EU MDR, ISO-10...
A seasoned professional with a decade of experience, I am a Leader and Speaker in the field of Quality Assurance & Regulatory Affairs, ...
I performed inspections and premarket approvals for FDA for 7.5 years. I am now a Senior Consultant operating out of Switzerland. I operate a...
An accomplished, versatile, results-oriented clinical research professional with over 14 years of experience in the Pharmaceuticals & M...
I am a medical student (UF) with a masters in medical innovation (UC Berkeley and UCSF). I have been working part-time as a medical product con...
We are a Contract Research Organization (CRO) that focuses on advanced project management, clinical operations, medical writing, statistical an...
I am a freelance medical, scientific, and technical writer with high-quality researches at Harvard Medical School proven by research papers pub...
Qualifications: MBiochem Molecular and Cellular Biochemistry, Oxford University PhD Haematopoetic Stem Cell Gene Therapy, University of Manches...
Fourteen years of R&D, Regulatory and Medical writing experience in various disciplines across In-vitro diagnostics, medical device regulat...
PhD, postdoc, senior researcher in medical physics, imaging, radiotherapy. Extraction of attributes from real-world collected data. Medical Im...
On Kolabtree, I offer publication, grant writing, and conference support medical writing services, including conference abstracts, peer-reviewe...
Doctor in Engineering specialised in medical devices research and development. Focused on validation and verification of development processes ...
A competent pharma professional with +10 years of experience in Scientific and medical writings, Regulatory intelligence, DRA, F&D, MSAT, a...
It's me Dr.Hamdan, professionally computational biologist. My profession, not only professionally, but my passion is to interact with globa...
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PHD pharmacist, with more than 5 years of experience in Quality Assurance (QA) and Regulatory Affairs (RA). My experience enables me to help yo...
I have over 8 years of experience in Clinical Research, Regulatory Affairs and Quality Assurance of implantable and electro medical devices in ...
Mark Luhovy, MD is a medical doctor and biomedical engineer who has dedicated 20 years to the pursuit of understanding the intersection of medi...
Clinical Project Manager, Research and Development Technical Expert and University Lecturer. 7+ years in clinical research Studies: I have a b...
MDR and MDD Gap assessments and Remediation. Risk documents creation and all remediation process knowledge to get the CE mark for the product t...
Hi, I have 12 years of experience in a multinational Pharmaceutical and Medical Device company as a QA/RA manager. My Specialties -Experience...
Consult top freelance European medical device regulatory (mdr) specialists with expertise in regulatory guidance, regulatory systems, and more. Kolabtree is the world's largest platform for hiring trusted freelance scientists and consultants.
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