Top Freelance Post-Market Surveillance Experts for Hire

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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Madhu S.

Quality and Regulatory Affairs professional | Expert in CE marking, EU MDR 2017, FDA submissions & lead auditor ISO1...
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USD 30/hr
Advanced PG Diploma in CR & Regulatory Affairs (APGDCR-RA)
India

Over 7 years’ experience in Quality and Regulatory Affairs, and technical submissions for a range of medical devices, including Orthopaedics, S...

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USD 30/hr
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Nida A.

Experienced MDR and FDA certified CER/Technical File Writer with 7+ years of experience with multinational industries
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USD 50/hr
Law (LLB Honours)
Pakistan

An experienced clinical research and medical device Technical file writer who has certified on MEDDEV 2.7/1 Rev#4 documentation, EU MDR 2017/74...

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USD 50/hr
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Lisa R.

REGULATORY AFFAIRS - Medical Device - Biotech - Dietary Supplement - Pharma
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USD 200/hr
Certificate of Regulatory Affairs , Dietary Supplements and NHP
Australia

Highly motivated Product Formulation Expert and Regulatory Affairs Expert in the following fields: Medical Devices ,Pharmaceuticals ,Dietary Su...

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USD 200/hr
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Adam F.

exFDA Investigator / expert in Medical Device & Combination Product design, manufacturing, and compliance
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USD 200/hr
Bachelors of Science in Biochemistry
Switzerland

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...

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USD 200/hr
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Morgan B.

Medical writer with 7+ years of experience in clinical research
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USD 40/hr
MS
United States

Freelance writer with over 7 years in clinical research. I've been involved in medical device trials, drug trials, investigator-initiated s...

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USD 40/hr
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Danielle K. B.

M.D. | Clinical Research Professional | Medical Device | Pharmaceutical
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USD 60/hr
Medical Degree (MD)
United States

I am a clinical research professional with 6+ years of experience in the various therapeutic areas and industries including Respiratory, Anesth...

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USD 60/hr
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Dr. Roy A.

Ph.D. Eng. in control systems and biomedical devices | Author of 100+ research papers | Editor of 5 books
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USD 20/hr
Ph.D. Engineering
Lebanon

I am a full professor at La Sagesse University and the head of the Mechatronics and Biomedical Engineering Departments. My research focuses on ...

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USD 20/hr
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Dr. Hatem D.

Statistician and Data Analyst | Expert in Medical device ,Beauty and pharmaceutical products (Filler -Botox-PRP-etc)
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USD 250/hr
Masters of Pharmacy
United Arab Emirates

Statistician and Data Analyst | Expert in Medical device ,Beauty and pharmaceutical products (Filler -Botox- PRP -etc) , with 15+ years of expe...

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USD 250/hr
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Dr. Daniel P.

Freelance Market Access Consultant for Pharmaceutical products (CH, A)
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USD 150/hr
Dr. med.
Croatia

Trained Physician with clinical and 10+ years of practical experience in Market Access and Life Cycle Management of pharmaceutical products in ...

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USD 150/hr
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Dr. Chi Wut W.

8+ years of experience in bench work, biostatistics, and bioinformatics | Expert in R and Python
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USD 100/hr
Ph.D., Pharmacology
United States

Pharmacology PhD; Ongoing research on diabetes and colorectal cancer; Cell/ tissue engineering; biostatistics and bioinformatics

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USD 100/hr
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Darshan D.

Medical Writer || Clinical Researcher || Market Researcher || Digital Marketer || Health-Tech Start-up Consultant
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USD 50/hr
Master in Pharmacy
India

Seasoned Pharma Professional (12+ Years) with a demonstrated history of working in diversified profiles from a registered pharmacist, Productio...

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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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Sonali S.

Experience in EUMDR, 510k submission, Risk management file, ISO 13485
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USD 20/hr
Bachelor of Pharmacy (Gold Medallist)
India

Having experience in medical device regulatory affairs, EUMDR, USFDA 510K, ISO 14971, ISO 13485

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USD 20/hr
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Peggy G.

Senior Medical Writer at Medtronic
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USD 95/hr
Medical and Scientific Writing
United States

Having over 20-years’ experience working in nursing and public health research, I turned my focus to medical writing almost a decade ago. I ha...

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USD 95/hr
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Manas K.

Consult/Interim/FT: Plan, Execute: Strat Mktg, NPI/NPD, Intl Biz - Device, Diag, IVD, POC, Tele, Wearable, Cybersecurity
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USD 195/hr
Continuing Education Courses, Certificates, Training: FDA 510K, MDR; NPD, CRM, Finance; CDx, MDx, Strategy
United States

20+ years of planning, developing, executing, managing global strategic upstream marketing initiatives including developing roadmaps for portfo...

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USD 195/hr
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Omnia T.

Expert Medical Writer | M.Sc. in Medical & Molecular Oncology | Medical Communications | Academia
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USD 35/hr
Masters in Medical Biotechnology
Egypt

My name is Omnia and I am an Assistant Lecturer & Medical Writer with 6+ years of experience in the academic and professional sectors. I ho...

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USD 35/hr
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George M.

am an accomplished medical writer with a degree in Clinical Medicine and Community Health. My strong background in healt
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USD 20/hr
Bachelor of science in clinical Medicine and community Health
United States

As a medical writer with a degree in Clinical Medicine and Community Health, I leverage my expertise to craft high-quality content for healthca...

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USD 20/hr
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Megha B.

Health Economics, Market Access, Systematic Literature Review, Meta analysis (15+ years experience)
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USD 100/hr
Economics
United States

I have 15+ years of experience in health economics and outcomes research (HEOR) and market access in the US and globally. I have prepared healt...

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USD 100/hr
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Nisha N.

Clinical Research Professional with More Than A Decade Of Industry Experience (CRO, Site, And Academic Set-Up)
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USD 60/hr
Master of Science: Biochemical Pharmacology
Australia

• Experienced Clinical research professional, with the strong academic foundation of Graduation in Pharmacy and Post-graduation in Biochemical ...

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USD 60/hr
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Kunle A.

Food scientist with 7 years of experience in regulatory consultancy, Technical Writer in SOP, Contract manufacturi
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USD 50/hr
BSc in Food Technology
Nigeria

I am a food scientist with 7years of experience. I have BSc in Food Technology and member Institute of Public Analyst of Nigeria (MIPAN). My e...

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USD 50/hr
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Dr. Jason B.

Skilled Chronic Disease and Medical Device Researcher
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USD 75/hr
Ph.D.
United States

Experience in epidemological research methods, statistics, and cardiovascular disease. 15+ Year track record of company internal and external ...

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USD 75/hr
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Dr. Vera M.

Clinical Research - Drug & Medical Device development and regulatory compliance (GCP/GLP/ISO 13485) - Expert Consult...
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USD 200/hr
Post-Doc
United States

Providing leadership and strategic direction in Drug/Medical Device Development and Quality assurance to meet the new Industry challenges Leade...

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USD 200/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. Dilip B.

Endorsed by the Royal Academy of Engineering as having exceptional Talent in Biomedical and Medical sciences
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USD 150/hr
PhD, Neuroscience
United Kingdom

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 ...

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USD 150/hr
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Kolabtree is the leading online marketplace for Post-Market Surveillance experts. Post your project, get bids, and hire qualified experts quickly and easily.

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We take several measures to help you work with full confidence and peace of mind.

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Restrict who can see your project and send you proposals. Invite only specific freelancers to view your project.

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Our T&C include a default confidentiality clause that protects your IP and NDA for added protection before disclosing project details.

Kolabtree ensures safety and security of your payments and personal information and project details. Kolabtree’s T&C includes a default confidentiality and NDA clause.

You will receive detailed proposals directly from Kolabtree. These proposals will include a comprehensive Statement of Work (SOW), project fees, milestones, and deadlines.

You can choose to pay either a fixed or an hourly fee based on your scope of work. Pre-pay for the next milestone. You have to approve the deliverables only if the quality meets your expectations. If you arn’t happy, we’ll refund your money.

Kolabtree will share multiple quotations for your project. You have the freedom to accept the quote that aligns with your project requirement and budget. You can get in touch with us in case you want to discuss the fee.

Our T&C include a default confidentiality clause that protects your IP and NDA for added protection.

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You have to approve the deliverables only if quality meets your expectations. If you arn’t happy, we’ll refund your money.

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Pre-pay for your project and work with the expert to get your desired output. Keep track of files and conversations in the user-friendly Workspace.

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Job Done!

Approve the deliverables once you're satisfied with the job done.