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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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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Madhu S.

Quality and Regulatory Affairs professional | Expert in CE marking, EU MDR 2017, FDA submissions & lead auditor ISO1...
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USD 40/hr
Advanced PG Diploma in CR & Regulatory Affairs (APGDCR-RA)
India

Over 10 years’ experience in Quality and Regulatory Affairs, and technical submissions for a range of medical devices, including Orthopaedics, ...

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USD 40/hr
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Dr. Marco C.

Associate Professor in Medicine with 10+ years of experience in medical/scientific writing
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USD 8/hr
Postgraduate Degree in Anesthesiology, Intensive Care, Pain Management
Italy

I am a seasoned medical professional and researcher with expertise in the realm of medical writing. Over the years, my experience has encompass...

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USD 8/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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Dr. George M.

Clinical Researcher/Market Analyst/Medical writer with a degree in Clinical Medicine .
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USD 30/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 30/hr
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Dr. Hafsa I.

Medical Device Regulation (MDR) - BER - Technical File - CER - ISO13485 - Production manager - SOPs - Design File - GRIN
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USD 35/hr
PhD Biomedical Sciences
Pakistan

Medical Device Production Manager with 5 years of experience in device development - Technical file - Design File - Procurement - Technology De...

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USD 35/hr
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Dr. Azza G.

Medical Regulatory Writer and Editor, Clinical Evaluation Specialist
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USD 25/hr
PhD
Germany

Ph.D. trained clinician with expertise in bone biology, inflammation, and osseointegration. Established a career as a medical writer three year...

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USD 25/hr
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Dr. Tia W.

Freelance Clinical Research Expert with 8+ years experience in management, study design, budgeting, medical writing risk
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USD 90/hr
Bachelor of Science Biology
United States

Dr. Tia Warrick is an accomplished clinical research professional with 8+ years of experience providing strategic, managerial, and operational...

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USD 90/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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Judit P.

MSc in Pharmaceutical Design | Ready to turn your work into narrative
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USD 20/hr
MSc
Denmark

Scientist with lab experience in protein and antibody engineering, cancer and infectious diseases. Currently doing my PhD in advanced antibody ...

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USD 20/hr
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Eric D.

A clinical operations expert with over 25 years of experience in global clinical strategy and execution.
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USD 225/hr
Bachelors
United States

Over 25 years of experience in all facets of clinical research including with a focus on early phase medical devices and combination products. ...

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USD 225/hr
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Johannes e g Hans V.

Global Expert in Quality engineering management, Auditing, and Regulatory Compliance, SQE. Delivering results for proces
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USD 125/hr
BSc Engineering
Netherlands

Eager to contribute with my passion for quality improvement, attention to detail, and auditing expertise, ensuring success process architecture...

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USD 125/hr
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Minh Tuan T.

High-achieving individual with 4+ years in medical device regulations (EUMDR & FDA) and business process development...
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USD 85/hr
Masters of Science
United States

Regulatory and Clinical Affairs Maintained strong customer relations, providing exceptional on-site technical, clinical, and sales support to o...

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USD 85/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. 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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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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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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Anjali S.

Experience in Clinical Research & Development, Pharmacovigilance, QAQC, Medical and Medico and content writing
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USD 50/hr
Masters in Pharmacology( M. Pharm)
India

Performance-driven professional with total 2 decades of rich & extensive experience in Clinical Research & Development, Pharmac...

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USD 50/hr
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Mahasweta G.

Well read, updated science communicator for all audiences
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USD 50/hr
M Tech - Biomedical Engineering
India

A thorough professional trained in Science, Technical, Engineering, and Medical Research Publishing, I have 3+ years in online publishing. Key...

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USD 50/hr
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Bharti S.

Scientific & Medical writer, COVID-19 virologist, Journal manuscript writing, Editor, Research papers, clinical tria...
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USD 102/hr
Master of Public Health (M.P.H.), Fundamentals of Clinical Trials
India

A strong background in virology, medical microbiology and public health qualifies me to work on COVID-19 projects (factsheets, COVID-19 at home...

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USD 102/hr
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Dr. Ritesh Khandelwal M.

Clinical Research Professional with 11+ yrs. of experience in Clinical Trials, Medical Writing, Statistical Analysis CDM
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USD 350/hr
Msc Clinical Research
India

I have an experience in Research Projects planning, designing to execution in Cardiology, Gastrology, Neurology, Opthalmology, Oncology, Endoc...

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USD 350/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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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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Contact experts directly

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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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Keep track of files and conversations in the user-friendly Workspace.

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Collaborate

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Job Done!

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