Top Freelance Medical Device Regulatory Specialists For Hire

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 freelance science and medical writer who helps medical device and pharmaceutical companies create evidence-based content for physicians,...

We are a Contract Research Organization (CRO) that focuses on advanced project management, clinical operations, medical writing, statistical an...gt; Feasibility survey reports, disease demographics > Standalone QC and review of documents Publicationwriting services include: > Publication planning > Primary and secondary manuscript writing

Experienced Quality and Regulatory Affairs professional with an experience of working in the medical device industry. Skilled in medical device...

An accomplished, versatile, results-oriented clinical research professional with over 14 years of experience in the Pharmaceuticals & M...

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...

A passionate lifelong student of Biomedical sciences with a Master’s degree from Carnegie Mellon University (CMU), I have always been fascinate...

I am a pharmacist and a professional medical writer with over 11 years experience in various medical/pharmaceutical sectors including: researc...

A strong background in viorology, medical microbiology and public health qualifies me to work on COVID-19 projects (factsheets, COVID-19 at hom...A strong background in viorology, medical microbiology and public health qualifies me to work on COVIDtop rated writer & editor with emphasis on medical writing, scientific journal manuscripts, public

Scientific Writer with 9+ years of experience with a demonstrated history of working in the Medical Device domain, SME in Clinical Evaluations ...

Focused on new EU MDR. Clinical reviewer for the MD evaluation/investigation; PMCF; Clinical data, Clinical, biological, PMS evaluation/investi...

1. Preparation of Clinical Evaluation Reports (CERs) in accordance with Medical Device Regulation (MDR) and 93/42/EEC Medical Device Directive ...

Qualifications: MBiochem Molecular and Cellular Biochemistry, Oxford University PhD Haematopoetic Stem Cell Gene Therapy, University of Manches...

PhD, postdoc, senior researcher in medical physics, imaging, radiotherapy. Extraction of attributes from real-world collected data. Medical Im...

- I am a passionate and creative innovator with an entrepreneurial character and with a good feeling for quality. - I combine organizational kn...

Doctor in Engineering specialised in medical devices research and development. Focused on validation and verification of development processes ...

A clinical research scientific writer with medical and regulatory CER expertise in MEDDEV 2.7/1 rev4 documentation, EU MDR and FDA compliance. ...PRISMA), Google Scholar; Excellent technical skills: peer-reviewed scientific publications, scientific

I am a freelance medical, scientific, and technical writer with high-quality researches at Harvard Medical School proven by research papers pub...

Biomedical engineer with 4+ years of experience in collaborative research (medical imaging for nuclear medicine applications) and several years...imaging for nuclear medicine applications) and several years of strategic management of scientific publicationspolicy to meet ICMJE and GPP3 guidelines, standardized publication planning and timeline management,collaboratively adapted new research procedures into internal processes (study contract updates for publicationat conferences/in journals vs previous year) ★ Coordinated efforts and resources to deliver timely publicationsFollow-up of publication processes from draft to publication (~20/year) ★ Bridged between the technical

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...

Medical Communications Consultant -Writing Clinical Evaluation Reports (CER) for medical device manufacturers -Preparation of clinical reports ...

A seasoned professional with a decade of experience, I am a Leader and Speaker in the field of Quality Assurance & Regulatory Affairs, ...

Mark Luhovy, MD is a medical doctor and biomedical engineer who has dedicated 20 years to the pursuit of understanding the intersection of medi...

I have more than 6 years experience (research and pharmaceutical industry) with a long track of success. My years as a researcher provided me ...

Nanotechnology and Medical Device enthusiast with experience in New Product Development, Regulatory Affairs and Quality Management System. Work...