Hire Freelance Clinical Trial Protocol Writing Experts

Dr. Ahmed E.

Freelance Medical Writer and Biostatistician with 5+ years of experience in clinical research
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USD 70/hr
MPhil PhD Student
United Kingdom

An MD with an onging Ph.D. in Healthcare Data Analytics....I have extensive experience within the scope of scientific writing, peer-reviewed publications, advisory...

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USD 70/hr
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Dr. Maartje W.

Experienced Medical and Science Writer and Editor - Specialized in Oncology, Immunology, Gynecology, and Healthy aging
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USD 150/hr
PhD
Canada

I am a freelance medical and science writer with over 10 years of biomedical research and medical writing experience in oncology, immunology, a...

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USD 150/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. Diksha V.

Researcher & Writer with 11+ years of experience in biotechnology, biomedical, bioinformatics and product developmen...
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USD 100/hr
PhD
India

I am a doctorate in life sciences with an experience of over 11 years in the academic and corporate sector. I have managed projects focusing o...

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USD 100/hr
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Cristal R.

Medical doctor with 5+ years of clinical research, medical writing and biostatistical analysis experience.
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USD 25/hr
Postgraduate in Principles and Practice of Clinic Research Program
Dominican Republic

I am a medical doctor holding a postgraduate in Principles and Practice of Clinical Research, accompanied by advanced expertise in biostatistic...

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USD 25/hr
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Dr. JORDANA S.

Ph.D. student in pharmaceutical sciences ǀ Pre-clinical/Clinical studies ǀ Innovation ǀ Entrepreneurship ǀ Biotech
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USD 10/hr
M.Sc. Physiological Sciences
Germany

B.S. in biomedicine, M.S. in physiological sciences, and Ph.D. student in pharmaceutical sciences. I have experience in preclinical and clinica...

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USD 10/hr
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Dr. Tatiana M.

Medical writer with 14+ years of experience in clinical research.
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USD 65/hr
Doctor of Medicine (MD)

Medical writer specializing in clinical protocol development, informed consent form (ICF) creation, case report form (CRF) design, investigator...

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USD 65/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. 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. Hrishikesh G.

Over 30 years of experience commercializing medical devices for large, mid-size and early stage companies.
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USD 125/hr
PhD in Electrical Engineering
United States

Broad hands-on software and hardware development for medical devices such as diagnostic imaging devices (PET, MRI, X-Ray and Ultrasound), blood...

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USD 125/hr
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Dr. Scott A.

Medical doctor and medical affairs professional with 8+ experience in academic, preclinical and clinical research
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USD 50/hr
Medical Degree (MD)
Canada

Medical affairs professional with 6 years of experience in the pharmaceutical and medtech industries and 10 years of experience in academic an...

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USD 50/hr
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Dr. Thor N.

Medical Consultant with 25+ years generating medical information for mutually agreed projects within the health area.
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USD 45/hr
Master in Business Administration
Mexico

I am a medical doctor, specialized in Family Medicine, with a degree in Clinical Pharmacology, and an MBA in Quality Administration. I worked i...

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USD 45/hr
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Dr. Marijn L.

Principal investigator | IRB member | Human neuropsychopharmacology of psychiatric disorders | Clinical trial specialist
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USD 100/hr
PhD, Neuropsychopharmacology
United States

I have close to 20 years of experience in human neuropsychopharmacological research at the Department of Psychiatry and Behavioral Sciences. I ...

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USD 100/hr
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Dr. Muhammad Hashim G.

Academic Writing | Clinical Trials | Research | Manuscript Writing | SPSS | Proposal Writing | PPT Presentations | SLR
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USD 70/hr
Pulmonary Rehabilitation Certificate
Pakistan

A doctor by profession, a researcher by passion & a staunch believer in the practice of evidence based medicine and clinical research, ...

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USD 70/hr
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Krishna K.

Medical Writer with Masters degree and 11+ years of experience in clinical research in multinational pharma companies.
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USD 40/hr
Master in Pharmacology
United Arab Emirates

Clinical Project Management and Medical Writing professional with 11+ years of experience in bio study activities including project planning, m...

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USD 40/hr
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Dr. Rajesh G.

Medical Researcher and Journal Editor | Expert in clinical data analysis
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USD 35/hr
MDS
Nepal

I am working in a medical institute for 9+ years as faculty orthodontist. Currently, I am Associate Professor with responsibility including aca...

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USD 35/hr
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Dr. Kanika S.

Certified Medical/Scientific Writer and editor
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USD 75/hr
Medical Writing
United States

I am a PhD-trained medical writer copyeditor with over 4 years of experience. I hold a graduate-level certification in Medical writing and edit...

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USD 75/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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GURUDATH G.

Freelance clinical research leader and project/program manager - 13+ years of experience
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USD 100/hr
M. Sc - Clinical Research
India

Entrepreneur, Design Thinking Master Practitioner & Human-centred Innovation enabler Clinical Research Leader with 8+ years of Project,...

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USD 100/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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Joshita M.

Biomedical Engineer, CMU | Product Manager & Medical Writer | Expert in Clinical Research with 9+ years of experienc...
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USD 30/hr
MS - Biomedical Engineering
Netherlands

A passionate researcher, with a Master’s degree in Biomedical Engineering from Carnegie Mellon University (USA), I have 9 years of product deve...

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USD 30/hr
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Alifiya T.

Clinical Research Scientist & Medical Writer with 5+ years of experience in academia & pharmaceutical industry
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USD 10/hr
Master of Public Health (Epidemiology & Biostatistics)
United States

I am a research scientist/medical writer trained in clinical sciences, epidemiology and biostatistics (BDS, MPH, Rutgers University, USA). My p...

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USD 10/hr
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Rudra P.

Group of Clinical Research Professionals (Project Manager, Biostatisticians, CRAs, Medical Writers, SAS Prgmers)
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USD 70/hr
MS
India

We are a Contract Research Organization (CRO) that focuses on advanced project management, clinical operations, medical writing, statistical an...

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USD 70/hr
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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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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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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.