Hire Freelance Clinical Trial Protocol Writing Experts

Dr. Adam S.

Scientist and medical writer with experience writing clinical and regulatory documents, publications,
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USD 100/hr
PhD
United States

Experienced scientific and medical writer with expertise in clinical writing (clinical trial protocol, CSR, IB, ICF) and regulatory writing (IN...

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USD 100/hr
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Dr. Fanny L.

PhD Immunology | Pharmacy | Scientific communicator 10+ yrs of experience in biomedical research | Analyst | Manager
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USD 100/hr
Pharm D
United States

PhD scientist in Immunology and Pharmacist, I dedicated my research on eosinophils, eosinophil associated diseases, and targeted immunotherapie...

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USD 100/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. Oyinkansola S.

Medical Doctor and Writer: Bridging Knowledge and Communication in Healthcare
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USD 40/hr
MPH
United Kingdom

Overview: As a dedicated Medical Doctor and accomplished Research Writer, I bring a unique blend of medical expertise and writing proficiency ...

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USD 40/hr
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Dr. Dhaval P.

Medical Writer with 5+ Years of Experience in Clinical Research
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USD 30/hr
PhD in Pharmacology
India

I am a PhD graduate with pharmacology specialization and have experience in handling clinical trial protocols, Clinical study reports, Manuscri...

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USD 30/hr
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Dr. Pari J.

Medical Advisor/Clinical Research professional with PhD and 10+ years of global experience in Healthcare Industry
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USD 90/hr
PhD - Pharmacology
Australia

Digital Health an Medical/Scientific Affairs professional holding a Ph.D. degree in pharmacology with extensive academic and industry experienc...

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USD 90/hr
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Dr. Payam P.

Pharmacoepidemiologist and Data Analyst/Expert in Pharmacovigilance,Clinical Trial, SPSS/R Software,Scientific Writing
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USD 70/hr
PhD in Pharmacology (Pharmacoepidemiology)
Netherlands

-Postdoctoral Researcher of University of Manitoba -Postdoctoral Researcher of Erasmus Medical Center, Rotterdam, Netherlands. -Postdoctoral R...

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USD 70/hr
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Dr. Ana Carolina E.

PhD in Neuroinflammation from UCL, independent biomedical researcher, medical software and clinical trials.
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USD 50/hr
PhD in Ophthalmology (Neuroinflammation)
United Kingdom

PhD graduate with 6+ years of biomedical research experience in immunology, vascular biology and auto-immune diseases. Experience in phase III/...

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USD 50/hr
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Dr. Tanima B.

Freelance ocular immunologist & Data Analyst | Expert in scientific writing with 10+years of experience.
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USD 50/hr
PhD
Germany

I bring to the collaborators an enthusiasm for creating knowledge with 15+ years of experience in the field of Biology, excellent project manag...

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USD 50/hr
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Dr. Sharjeel A.

Pharmacist | Health Wellness | Medical Writer
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USD 10/hr
MPhil
Pakistan

I have a degree in pharmaceutical science and a solid background in writing for various clients throughout my freelance writing experience. Whi...

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USD 10/hr
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Dr. Kiran C.

Medical Writer with 5+ years experience in clinical research
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USD 65/hr
MPH
Canada

Experienced Medical Doctor and Clinical Research Associate with a demonstrated history of working in the medical practice industry. Skilled in ...

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USD 65/hr
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Dr. Vera Bin San C.

Regulatory Medical Writer with 10+ year of Scientific Publication Experience | Eye on Biostatistics Det...
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USD 90/hr
PhD
France

Are you looking for a medical writer who can prepare regulatory submissions for an investigational medicinal product (IMP), e.g. clinical resea...

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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. Dayene C.

PhD and Masters in Biological Science (Respiratory Physiology). Background in Clinical Trials and Science Writing.
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USD 30/hr
PhD Visiting Researcher
Brazil

Experience with: Clinical Trials Phase I-IV, Lung Therapy and Toxicology, Respiratory Disease (including COVID-19), Cell Therapy (Stem Cells), ...

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USD 30/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. 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. Muhammad Usman M.

Medical content and copywriter
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USD 15/hr
Medical Writing
Pakistan

I am an experienced and professional medical content writer, copywriter, article/blog writer, and a scientific researcher with a keen interest ...

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USD 15/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. Marjana S.

Freelance scientific researcher with expertise in both clinical and preclinical sciences, including industry & acade...
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USD 120/hr
PhD
United States

I am an accomplished research scientist and group leader skilled in design of human and animal studies, in developing and reviewing IRB documen...

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USD 120/hr
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Dr. Gabriela L.

Medical writer | Scientific consultant | Biostatistics analyst
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USD 25/hr
MSc in Pharmacology
Brazil

I have a master's and a doctorate in Pharmacology, a post-bachelor degree in Regulatory Affairs and a bachelor's degree in Pharmacy. I ...

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USD 25/hr
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Dr. Reymart S.

Research and Development /Regulatory Writer / Editor with years of experience in clinical research and chemistry
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USD 60/hr
Diploma in Advanced Biotechnology
Philippines

Dynamic and goal-oriented chemist with more than 10 years of product development and experimental design and 5-years of experience in writing a...

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USD 60/hr
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Dr. Nagarjuna D.

Expert in Nucleic acid extraction, qPCR, Antimicrobial Susceptibility testing, Bacterial genomics
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USD 15/hr
Doctoral Program
India

Bacterial Growth monitoring assays, Developing Antimicrobial susceptibility testing systems, Extraction of cell free DNA from Blood. Designing...

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USD 15/hr
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Dr. Maicel M.

I am a medical doctor and researcher in the field of clinical trials, epidemiological research and data science.
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USD 50/hr
Biostatistics specialist
Cuba

I have experience in the preparation of analysis plan and statistical processing report. I perform statistical processing in R, SPSS, Python, E...

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USD 50/hr
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Ana Carolina F.

Brazilian journalist / health researcher, expert in: qualitative and formative research & randomized controlled tria...
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USD 20/hr
Doctor in Science
Brazil

In order to promote safer and more positive childbirth experiences for women, for the last...nine years I've collaborated in qualitative and quantitative research projects in the areas of: public...

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USD 20/hr
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Dr. Srishti N.

Neuroscientist | Biomedical scientist | Scientific consultant | Medical communicator | Research strategist
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USD 50/hr
Doctor of Philosophy
India

"Research isn't complete until it has been communicated." A personal motto that has driven my passion for effective scientific c...

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USD 50/hr
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Consult top freelance clinical trial protocol writing specialists with expertise in protocol development, clinical research writing, and more. Kolabtree is the world's largest platform for hiring trusted freelance clinical trial protocol writers.

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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.

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How to Hire an Expert in Clinical Trial Protocol Writing

All clinical trials for drugs and medical devices require the preparation of a clinical trial protocol, which is a document describing the trial rationale, objectives, design, organization, and methodology, as well as ethical and statistical considerations. Clinical trial protocols need to adhere to the guidelines for Good Clinical Practice (GCP) according to the International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH). These documents also need to conform to the requirements of the relevant regulatory agencies (e.g., FDA, EMA) and institutional review board (IRB), who apply rigorous review before the trial sponsor being allowed to conduct the study.

Investing time and expertise into developing a good research protocol that is compliant and scientifically sound is critical to the success of the entire trial, and it can save a lot of time and expense in the long run. It can avoid the trial being put on hold or requiring timeline extensions, or worse yet, generating inconclusive data and resulting in trial failure.

What Does a Clinical Trial Protocol Writer Do?

Clinical trial protocols require input from a multi-disciplinary team of medical and operations professionals that may include the study sponsor, a clinician, a statistician, the clinical research coordinator, the project manager, and a medical writer. It is the medical writer’s role to incorporate all of these inputs into the final clinal trial protocol (CTP).

The responsibilities of a clinical trial protocol writer can include:

  • Applying protocol content guidelines and templates
  • Writing up the protocol synopsis and the full research protocol
  • Researching published and unpublished medical and scientific data to support the study rationale and approach
  • Working with the study sponsor and other team members to develop, review, revise, and finalize the clinical trial documentation
  • Ensuring compliance of the protocol to regulatory and ICH guidelines
  • Ensuring compliance of the protocol to IRB guidelines
  • Preparing scientific and regulatory documents to support ongoing clinical research trials

 Experts in writing clinical trial protocols will typically be medical writers with several years of experience writing for a contract research organization (CRO), pharmaceutical company, or biotechnology company. They usually have a PharmD, MD, or a Master’s or Ph.D. degree in an allied scientific field. They will have extensive knowledge of the regulatory requirements relevant to their region (e.g., FDA or EMA), as well as the ICH guidelines.

Clinical trial protocol writers work either as freelance medical writers or for CROs, medical device or healthcare companies, clinical research consultancies, and pharmaceutical companies. The job titles of clinical trial protocol writing experts vary and can include Medical Writer, Research Medical Writer, Senior Medical Writer, Principal Medical Writer, Clinical Research Consultant, and Clinical Research Communications Specialist. While some may be generalists, others may specialize in e.g., biologics or medical device protocol writing.

How Much Does It Cost to Hire a Freelance Clinical Trial Protocol Writer?

To hire a freelance clinical trial protocol writer, the fee generally ranges from 40100 USD per hour depending on the required skillset and the level of experience necessary.

The hourly fee can be negotiated upfront based on the estimated number of project hours, or a flat fee (for projects of a defined scope) can be discussed. If you need short-term/temporary access to these specialists, then hiring a freelance clinical trial protocol writer or clinical research consultant on our platform is a convenient and cost-effective way to harness their expertise.

How Do You Write an Effective Job Post to Hire a Clinical Trial Protocol Writer?

The best way to attract the top Kolabtree freelancers in this field is to make your project description informative. You will need to provide information on the following:

  • Skills required (e.g., expertise in writing medical device protocol writing)
  • What the project area is (e.g., orthopedic devices)
  • What the project entails (e.g., ensuring protocol compliance with EMA regulatory guidelines)
  • What the deliverables are (be specific about what you need the outputs to be)
  • Duration of the project (provide an estimate of how many hours work you will need per week/by when you need the project to be completed)
  • By when you need to hire (having more leeway on this will give you more time to choose the best expert for your needs)
  • Your budget (per hour or fixed fee)

If you are unsure what exactly is required, providing as much detail as possible will allow the experts to still make an informed bid for your project and suggest the best routes forward.

Our platform makes it easier than ever before to connect and collaborate with medical writers with experience in clinical trial protocols.

Hire Clinical Trial Protocol Writers by posting a project for free.