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Top Freelance Clinical Trial Documentation Experts for Hire

Dr. Anurag G.

Medical Writer & Researcher | Literature Reviews | Protocol Writing & Editing Manuscripts, Protocols, CSRs, Pres...
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USD 43/hr
Doctor of Pharmacy (Pharm.D.)
India

As a medical researcher qualified with advanced Pharm.D. training, I bridge the critical gap...between complex scientific data and the clear, persuasive content required for regulatory approval, publication...

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USD 43/hr
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Dr. Brent R.

I sell FDA Compliant Drug Substance and Drug Product Quality and Performance Testing Programs & Guidance to FDA Appr...
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USD 225/hr
Juris Doctorate
United States

I own a consulting firm with over 70 years of experience throughout the entire lifecycle of pharmaceutical submissions. We ensure your Drug Sub...

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USD 225/hr
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Dr. Joyita B.

Creator & Content developer of Materials Data Explorer (https://bjoyita.github.io)/ | Materials Scientist
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USD 20/hr
PhD (Materials Science & Engineering)
India

I am a materials scientist. I earned my masters and doctorate degree in materials science and engineering from the Indian Institute of Science,...

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USD 20/hr
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Dr. Trinadh Venkata Satish T.

Experienced research scientist keenly interested in contributing to medical devices, health care and biotech projects.
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USD 50/hr
Postdoctoral Research (Department of Molecular Cellular and Developmental Biology)
Netherlands

Experienced Research Scientist with a Ph.D. and over 20+ years of demonstrated history of working in the areas of Tissue Engineering, Infectiou...

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USD 50/hr
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Dr. Natalie B.

Clinical researcher (PhD in Pharmacology) with 12 years’ experience spanning academia, Government and the private sector
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USD 75/hr
PhD - Experimental Pharmacology
Australia

• Solid knowledge of Good Clinical Practice guidelines, Medical Code of Conduct and local clinical trial regulatory requirements. • Medical an...

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USD 75/hr
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Dr. Geetanjali B.

Research Scientist with experience in Medical Devices, Pre-clinical Research and Writing
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USD 50/hr
PhD
United States

I am a Ph.D. in Bioengineering with expertise in medical device development and innovation, experimental design, data analysis and interpretati...

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USD 50/hr
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Dr. Loren D.

Medical writer/consultant
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USD 85/hr
Canada

Loren DeVito, PhD, is a science and medical writer with expertise across a wide range of therapeutic areas, including oncology, neurology, card...

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USD 85/hr
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Dr. Paula d.

Health Care, Regulatory Affairs & Safety Consultant
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USD 150/hr
BS- Nursing
United States

More than 17 years working as Health Care Consultant for different companies and agencies, as well as a professor from a private and public un...

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USD 150/hr
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Dr. Onkar S.

Medical Writer, Reviewer & Physician| Expert in Drug Development, Medical Affairs, Clinical Research, Regulatory &am...
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USD 30/hr
MD Pharmacology
India

Medical Doctor & academician turned into pharmaceutical professional. +15 years of experience with leadership positions in drug develop...

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USD 30/hr
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Ph.D. - Biochemistry and Molecular Biology
India
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USD 50/hr

Global professional, doctoral-level research experience in life sciences. Experienced in scientific writing, ICH-GCP E6 framework, clinical res...

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USD 50/hr
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Dr. Aissulu I.

Medicine, Medical Doctor, experienced in Clinical trial submission, QA, R&D, Academic Research, Public
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USD 100/hr
PhD in Pharmacology
Kazakhstan

CT: oncology, infections, gastro, gynecology, diabetes, CV; Public Health - policy, HTA, QA; Project Management in Regulatory submissions, CT, ...

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USD 100/hr
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Dr. Pharmanalytics S.

Freelance in pharma domain having specialization in generic market and expertise in the analytical and regulatory,
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USD 30/hr
Doctors in Analytical chemistry
India

Having an experience of more than 15 years in the analytical and regulatory domain with sound technical understanding to fulfill different regu...

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USD 30/hr
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Dr. Samundeeswari M.

PhD Scientist | Regulatory Affairs Associate (Medical Devices) | Technical Writing & Global Compliance
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USD 60/hr
Doctorate
India

I’m a PhD chemist with 9+ years of research experience in fluorine chemistry and radioactive materials, now transitioning into regulatory affai...

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USD 60/hr
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Dr. Girish D.

Medical writer with 14 years experience in regulatory writing, scientific writing, safety writing.
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USD 30/hr
Ph.D.
India

Prepare and review clinical and scientific documents that are part of regulatory submission including Clicical Study protocols, Clinical Study ...

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USD 30/hr
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Dr. Mohamad T.

Specialist in Cell and Gene Therapy manufacturing | Tissues Engineering | Analytical Development | Process Development
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USD 100/hr
Doctor of Philosophy (Ph.D)
Germany

I provide specialized consulting services to pharmaceutical and medical device companies with a focus on GMP compliance, CMC development, quali...

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USD 100/hr
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Dr. Gabriella G.

Clinical Protocol Writer, Clinical research professional, GCP and CCRP Certified, Scientific writer, Grant proposal
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USD 90/hr
PhD
United States

Goal-oriented biomedical research with more than 10 years experience and demonstrated achievement in managing clinical/translational research p...

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USD 90/hr
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Dr. Waqar L.

Auditing, Consulting, Training and Operations Management for International Standards i.e. ISO, BSCI, DIN, MDD, MDR, PPE
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USD 75/hr
PhD
Pakistan

Ten + years of hands-on technical working experience in the manufacturing environment covering Metal, Textiles, Food, Auto parts, Chemical proc...

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USD 75/hr
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Dr. Pierre L.

Healthcare technology development, 20 years engineering excellence + quality assurance & regulations navigation
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USD 155/hr
PhD industrial Engineering
Australia

If you are an entrepreneur/founder in health-tech, I can help you * fine tune your strategy * navigate science, engineering, quality processes ...

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USD 155/hr
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Dr. Sam M.

Certified and experienced professional medical/scientific writer with 18 years of experience
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USD 30/hr
Doctor of Philosophy (Ph.D, Pharmaceutical sciences)
India

I am a Doctorate (PhD) in Pharmacy, a Certified Medical Publication Professional™ (CMPP), a certified Information Mapping Professional™ (IMP) a...

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USD 30/hr
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Dr. Codette P.

One stop solution for end to end Life Sciences global Regulatory support.
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USD 50/hr
PhD
India

Codette Pharma Regulatory Analytics Pvt Ltd provides top-level global regulatory and clinical support to Life Science companies. We are experts...

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USD 50/hr
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Dr. Nitin M.

Scientific Advisor at Melior Life Sciences (CRO) | Consultant Radiologist | AI Research Advisor at Synapsica |
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USD 125/hr
MD
India

After completing MBBS from the All India Institute of Medical Sciences, New Delhi. He pursued MD in Radiodiagnosis from SMS Medical College and...

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USD 125/hr
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Dr. Sarika P.

The RAC qualified Regulatory Professional with more than 20 years of experience in the global regulatory submissions.
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USD 150/hr
Ph.D
India

The RAC-qualified Pharma Professional with more than 19 years of experience in regulatory, PV, and clinical research. Hold expertise in global ...

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USD 150/hr
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Dr. Javier G.

Experienced Medical Doctor and Freelance Medical Writer | Harvard-trained Researcher and Manuscript Writer
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USD 150/hr
Medical Doctor
Mexico

I am a highly skilled medical doctor with a passion for medical research and writing....With a strong background in clinical research and an extensive publication record in indexed medical...

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USD 150/hr
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Dr. Sheraz Hussain S.

Medical device regulations EU MDR 2017/745,Clinical evaluation ,ISO 13485 AND validation expert
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USD 335/hr
Doctor in Dental Sciences
Pakistan

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

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USD 335/hr
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Dr. Sudhansu Sekhar S.

Pharma Analytical Scientist, twelve years of experience in analytical research and regulatory responses i.e. FDA, EU etc
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PhD in Pharmacy
India

I have twelve years of experience in pharmaceutical analytical research. My core expertise is analytical method development by various techniqu...

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Dr. Randall S.

Biomedical Scientist, Writer and Editor, Life Sciences Consultant
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PhD Biomedical Engineering
United States

I am an ambitious and published scientist who is experienced in many scientific disciplines including Biology, Chemistry, and Engineering. I ha...

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Kolabtree is the leading online freelance marketplace for Clinical Trial Documentation experts. Post your project, get bids, and hire qualified experts quickly and easily.

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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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Job Done!

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