Hire Freelance Clinical Trials Specialists: Find Clinical Trial Consulting Services

Dr. Ana P.

Neuroscientist (PhD) combining 15 years of academic rigor with 6 years of neurotech leadership.
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USD 80/hr
Postdoc
Israel

- Scientific Consulting Services: * Scientific Due Diligence: Preclinical and clinical design validation, Mechanism of Action (MoA) analys...

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USD 80/hr
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Dr. Christine C.

Freelance Systematic Reviewer, Health Writer & Planetary Health Expert | 25+ years experience
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USD 80/hr
Doctor of Philosophy
Germany

I am a freelance researcher with 25+ years of experience in systematic reviews and evidence synthesis. I have worked for various institutions, ...

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USD 80/hr
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Amjad A.

Molecular Biologist | Medical Writing | Clinical Research, Metabolic Disease & Clinical Nutrition
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USD 50/hr
ICH-GCP E6 (R3): Quality, Compliance & Clinical Trial Management
Italy

Molecular biologist specializing in metabolic disease research, clinical trial design, and scientific communication. Expertise in MASLD/MASH pa...

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USD 50/hr
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ADHITHYA N.

Dentist | Periodontist | Implantologist | Medical Writer | Dental Content Writer | AI Annotator
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USD 20/hr
Master of Dental Surgery (MDS) - Periodontology
India

Assistant Professor of Periodontology | MDS Periodontist | Medical Writer | Dental Content Writer | AI Annotator I help dental clinics, healt...

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USD 20/hr
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Hossein M.

Computational Microbiologist & Medical Data Analyst
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USD 35/hr
Masters of Science
Turkey

"As a Ph.D. candidate in Medical Microbiology with over 14 years of hands-on clinical laboratory experience, I bridge the gap between trad...

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USD 35/hr
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Leila A.

Medical writer with 10+ years of experience in clinical research
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USD 30/hr
Full Professor/ Dr.
Iran

Research Focus Areas: Maternal and Perinatal Health: Research on pregnancy outcomes, breastfeeding, labor support, and infant health including...

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USD 30/hr
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Chindu E.

Drug Data Analyst | PV & Medical Writing Specialist | Regulatory Affairs | Evidence Synthesis & Pharma Data Cura...
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USD 15/hr
M.Pharm.
India

Drug Data Analyst and Published Clinical Researcher (NIPER, M.Pharm) with expertise in pharmacovigilance, medical writing, regulatory affairs, ...

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USD 15/hr
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Dr. Sardar Mohammed J.

Senior CMC & Analytical Chemistry Expert | HPLC/LC-MS, Impurities, Stability | PhD Peptide Chemist & Patent Hold...
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USD 55/hr
PhD
United States

I am a PhD-trained Analytical & Peptide Chemist with 20+ years of experience supporting global pharmaceutical, herbal, cosmetic, nutraceuti...

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USD 55/hr
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Dr. Faiz Ul A.

PhD Biomedical Scientist | Medical & Scientific Writer | Clinical Research & Biostatistics
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USD 40/hr
PhD in Biomedical Science
United Arab Emirates

I help clinicians, biomedical researchers, diagnostic laboratories, healthcare organizations, and life-science companies transform complex...scientific questions, research findings, manuscripts, and biomedical data into clear, accurate, and publication-ready...

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USD 40/hr
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Dr. Karine D.

Senior Biotech & Pharma Consultant | Medical Affairs, Scientific Intelligence & Medical Communications
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USD 130/hr
University Degree
France

PhD in Neuroscience with 20+ years of international experience across academic research, biotech startups and pharmaceutical companies, at the ...

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USD 130/hr
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Dr. Sherese F.

Medical Affairs, Clinical Strategy Consultant, Oncology, Neuro-Oncology, Clinical Trials, Evidence, MedTech
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USD 200/hr
PhD
United States

I am a PhD-prepared Medical Affairs and Clinical Strategy leader with more than 20 years of experience spanning oncology, neuro-oncology, clini...

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USD 200/hr
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Kay G.

Freelance (Bio)Pharma industry consultant/contractor (Expert Regulatory, Quality & Compliance - 30+ years experience...
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USD 72/hr
MBA
Canada

Industry consultant/contractor with extensive hands-on experience assisting offshore and domestic clients in bringing molecules to market. Sub...

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USD 72/hr
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Roberto P.

Cardiologist and Clinical Development Physichian with expertise in intervention, heart failure, and clinical trials
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USD 100/hr
Medical Degree (MD)
Portugal

Experienced Cardiologist and Clinical Development Director with a proven track record in interventional cardiology, advanced heart failure, and...

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USD 100/hr
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Larraitz L.

Bioinformatician & Data Analyst | Clinical Trials, Healthcare Data & Food Safety Expertise
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USD 35/hr
Bioinformatics for Health Science
Spain

Multidisciplinary life sciences professional combining a Bachelor's in Biochemistry and Molecular Biology, a Master's in Food Quality a...

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USD 35/hr
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Dennis P.

Medical & Regulatory Editor | Clinical Document QC | Scientific Editing & Fact-Checking
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USD 65/hr
Bachelors in English Literature
United States

I’m a highly experienced medical and regulatory editor with 20+ years of experience across clinical, regulatory, scientific, and promotional ma...

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USD 65/hr
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Dr. José F.

Clinical Research & MedTech Regulatory Consultant | ICH-GCP | ISO 14155 | EU MDR | Medical & Scientific Writer
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USD 96/hr
University Diploma in Applied Clinical Ultrasound (POCUS) for Emergency Medicine
France

Physician-scientist and senior clinical research consultant with more than 18 years of international experience across Europe and Africa, worki...

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USD 96/hr
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Mohammed H.

CER & Technical Writing Consultant | Clear, Evidence-Based Regulatory Documentation
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USD 45/hr
Bachelor in Pharmacy
India

I am a CER (Clinical Evaluation Report) specialist and technical writer with experience in developing clear, accurate, and evidence-based scien...

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USD 45/hr
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Dr. Anurag G.

Pharm.D. Medical Writer & Clinical Researcher | Regulatory Dossiers, High-Impact Manuscripts & Strategic CME
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USD 54/hr
Doctor of Pharmacy (Pharm.D.)
India

In high-stakes clinical and regulatory environments, the quality of your data is irrelevant if your documentation fails to satisfy a Notified B...

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USD 54/hr
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Work with the best clinical trial consultants on demand. Find freelancers for help with clinical trials consulting services, biostatistics, protocol writing and regulatory compliance.

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Kolabtree ensures the safety and security of your payments, personal information and project details. Kolabtree’s T&C include 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 aren'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 if 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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Job Done!

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

How to Hire a Clinical Trials Expert

A new treatment for a certain condition or disease is only made available to the general public after thorough testing is done through clinical trials. Those tests constitute scientific studies where a certain drug, substance, treatment or intervention is tested in real people.

In a clinical trial consultants, the investigator assigns participants to specific groups, which is typically done through randomization. Clinical trials are performed through different phases. They can be used for testing a new drug, a vitamin, a new diet, a less invasive surgical intervention, a diagnostic tool or even a medical device.

Before a clinical trial starts, it requires approval of an institution or health organization (such as the US Food and Drug Administration), which varies depending on the country where the trial is performed.

What Are the Phases in a Clinical Trial Protocol?

Testing of a new drug is focused on safety and effectives, which are usually performed through four distinct phases:

  • Phase I: the drug is tested on a small group of people to see if it is safe and to learn about its potential side effects, usually 20-80 people are included in Phase I clinical trials.
  • Phase II: the drug is tested on a bigger group for its effectiveness to treat a certain condition or disease. It also further evaluates safety and side-effects, usually with 100-300 people included.
  • Phase III: in order to learn more about the new drug, it is tested in different populations and using different dosages, sometimes combined to other treatments. It generally includes a few hundred people up to about 3000. If the clinical trial shows beneficial results and the drug is safe to be used by the general public, it is approved after phase III.
  • Phase IV: the drug has been approved and safety and effectiveness are monitored for longer periods of time for long-term effects.

What Can You Get From Freelance Clinical Trials Consulting Services?

Professionals who work with trials consultants usually gather a lot of expertise in this field. Grant applications, ethical approval, writing of articles based on clinical trial results and government approval are just a few of the areas where clinical research experts can help you.

Job titles include:  Clinical research associate, Biostatistician, Medical researcher, Clinical researcher, Healthcare research, Principal investigator, Research associate, Research consultant.

Why Should You Get Help From a Clinical Research Expert?

If you are conducting clinical studies for one of the most common reasons below, you might want to consider collaborating with a freelance clinical research expert.

  • Evaluation of one, two or comparing several treatment interventions, such as use of drugs, medical devices, health supplements, surgery and other types of therapy for treating a certain disease, condition or syndrome.
  • Learning about prevention or recurrence of a certain condition or disease, which can include use of different medicines, vitamins, vaccines, or even lifestyle changes, such as diet and exercising.
  • Evaluation of one, two or several diagnosing tools for a particular condition or disease.
  • Evaluation of different methods for identifying risk factors for a disease or condition.
  • Exploring alternatives to improve supportive and palliative care for people with a chronic and/or terminal disease.

How Much Does It Cost to Hire Clinical Trial Scientists?

Professionals specialized in clinical consultants are certainly in demand. For a minimum of 30-40 USD per hour, it is possible to collaborate with a freelance expert in this field. At Kolabtree you can also choose to pay a fixed rate for your entire project, which can be more cost-effective for longer projects.

How to Write an Effective Job to Hire Freelance Clinical Trials Specialists

Include the following in your job description so that you get proposals from relevant freelancers. 

  • Project description or scope of work: be specific about which phase for the clinical trials and what are the deliverables expected.
  • Duration of the project: specify if this is a short or long-term collaboration.
  • By when you need to hire: be clear if you are in a hurry to start with the collaboration.
  • Budget: can be paid per hour or per project.
  • Skills required: you should be looking for someone with experience in health care, pharmaceuticals, clinical research, and statistics, among others.

Hire Clinical Trials Freelancers by posting a project for free.