Top Freelance Investigational Device Exemption (IDE) Experts for Hire

Dr. Jalal A.

A Ph.D. scholar at Tsinghua University and academic writer by profession.
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USD 30/hr
Ph.D., Chemistry
Pakistan

I'll write scientific articles or reviews, abstracts, summaries, and assist you in your thesis, format and proofread it. Being a doctoral ...

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USD 30/hr
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Dr. Ahram Q.

Expert Life Science's Researcher, writer, and Consultant
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USD 50/hr
MPhil in Bioinformatics
Pakistan

My professional background is to technically write the Scientific content, assess the researcher in research work related to Bioinformatics and...

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USD 50/hr
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Dr. Ana Luiza C.

Freelance Medical writer, Clinical specialist and Regulatory affairs of Medical Devices, Ph.D. Biological Sciences
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USD 69/hr
MBA Quality Management
Brazil

I have over 8 years of experience in Clinical Research, Regulatory Affairs and Quality Assurance of implantable and electro medical devices in ...

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USD 69/hr
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Dr. SENTHILKUMAR S.

Helping Medical Device Companies as an SME in developing CEP, CER, PMS Plan, PSUR, PMCF Plan & Report and Manusc...
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USD 75/hr
Ph.D
India

Scientific Writer with 10+ years of experience with a demonstrated history of working in the Medical Device domain, SME in Clinical Evaluations...

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USD 75/hr
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Dr. Precious O.

Freelance Medical Writer with 5 year experience in Biomedical/Clinical Research
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USD 25/hr
Medical Degree (MD)
Nigeria

I am experienced in

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USD 25/hr
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Dr. Alan C.

Freelance innovative pharmaceutical and medical device market access and medical affairs
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USD 100/hr
PhD
United Kingdom

Market access for medical affairs, HEOR, payer facilitation, NICE/FDA implementation, budget impact modelling, HTA

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USD 100/hr
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Dr. Harsh V.

Medical/Scientific/Regulatory/Newsletter/CMC/Dossier/Research/Review/Thesis/Protocol/Report/Article writing & editin...
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USD 30/hr
PhD
India

A competent pharma professional with experience in Scientific writing, Regulatory competitive intelligence, DRA, F&D, MSAT and QA. Experie...

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USD 30/hr
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Peter O.

Experienced quality assurance and regulatory affairs professional in the medical device industry.
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USD 300/hr
MS Engineering Management
United States

Product experience includes Class 1, 2 and 3 devices: external defibrillators, AEDs, infusion pumps, patient monitors, image guidance, ventilat...

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USD 300/hr
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