Profile Summary
Mostafa A.
- Biostatistician & medical writer specializing in clinical research, pharmaceutical studies, systematic reviews, and meta-analyses - Found...
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Dr. Rui M.
Health policy researcher and EU grant writer with a PhD from the...University of Cambridge and nine years' experience at the intersection of biomedical research, public...
Dr. Nuvia P.
Medical Doctor specialized in Clinical Pharmacology with extensive experience in biomedical research, scientific writing, and academic teaching...
Madhu S.
I am a Regulatory and Clinical Specialist Medical Writer specializing in the preparation of high-quality scientific and regulatory documents fo...
Dr. Sary F.
I am a physician and Internal Medicine resident at the American University of Beirut Medical Center (AUBMC), with a dual background in clinical...
Arinayo A.
I am a Doctor of Public Health, Certified Clinical Research Professional, and research compliance executive with more than 15 years of experien...
Hiba I.
I'm a physician (MBBS) with a strong track record in systematic review and meta-analysis methodology, evidence synthesis, and medical writi...
Dr. Raymond H.
Dr. Raymond Haddad, MD, MHSc, PhDc, FPICS, is a physician with over a decade of clinical, academic, and scientific experience. He is an accompl...
Dr. Geraldo N.
I am a PhD-trained epidemiologist and Senior Researcher based in Czechia, with current work focused on multinational stroke and cardiovascular ...
Dr. Nihal E.
I am a Pharmaceutics Associate Professor with 15+...experience in DoE, formulation and Drug Delivery technology with proven track record and prestigious publications...
Deepak D.
Highly motivated Regulatory Affairs professional with strong expertise in U.S. FDA 510(k) submissions, Indian import licensing (CDSCO), ISO 134...
Dr. Prahatheeswaran G.
About Me I am a Specialist Physician, Public Health Epidemiologist, and Preventive Oncology Fellow with over 5 years of experience spanning cli...
Dr. Muhammad A.
I am a pharmacy and clinical research professional with extensive academic and research experience in pharmacotherapy, clinical pharmacy, geria...
Dr. Svitlana M.
Physician (MD) and Epidemiologist with 10+ years in clinical medical writing, biomedical research support, and scientific editing....With 30+ peer-reviewed publications and 50+ manuscripts shepherded through peer review, I turn raw datasets...
Thierry C.
A highly specialized Biostatistician/Statistician/data analyst with a proven track record in developing cutting-edge statistical frameworks for...
Ahmed S.
I help researchers and organizations turn clinical and biomedical data into reliable, interpretable insights. My expertise is in machine learn...
Dr. Carlos C.
I am a physician and PhD-trained health researcher with over 20 years of experience in evidence synthesis, health technology assessment (HTA), ...
Dr. Tresha R.
I am a PhD-qualified researcher in Yoga Science with a multidisciplinary background in Biomedical Engineering and Yoga Therapy. My expertise li...
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Dr. Raghunaathan R.
UK-based medical doctor with extensive experience in Trauma & Orthopaedics and postgraduate qualifications including MRCS, MSc Orthopaedics...
Quratul Ayn Z.
PhD researcher in Health Sciences specializing in meta-research, clinical trial methodology, and evidence synthesis. I have expertise in system...
Dr. Fabiana B.
I have a PhD in Medical Science and Data Analysis certificate with over 15 years of experience in the life sciences in biotech companies. I spe...
Dr. Tanvi D.
Pharm.D. graduate specializing in clinical data management and pharmacovigilance, with hands-on experience across ICMR-funded clinical research...
Dr. Runqi W.
Medical Writer, Manuscript Writing, Clinical Trial Protocol
Dr. Priyanka S.
I help biotech startups and research labs design, optimize, and validate low-cost multiplex diagnostic assays—fast. With a PhD in Virology and ...
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Oliver S.
As a former Post-Market Surveillance & Vigilance Manager at Mathys (Swiss manufacturer of artificial joint implants), I have extensive hand...
Work with the best clinical trial consultants on demand. Find freelancers for help with clinical trials consulting services, biostatistics, protocol writing and regulatory compliance.
We take several measures to help you work with full confidence and peace of mind.
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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 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.
Contact experts directly
Speak directly with freelancers and explain your requirements.
100% satisfaction guaranteed
You have to approve the deliverables only if quality meets your expectations. If you aren't happy, we'll refund your money.
Project Management
Keep track of files and conversations in the user-friendly Workspace.
Flexible, secure payments
You can choose to pay either a fixed or an hourly fee based on your requirement.
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Clinical trial scientists needed for a mini project$450.00
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Need a clinical trial consultant$500.00
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Freelance clinical trials consulting services needed$500.00
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Looking for a clinical trials advisor$550.00
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Hiring for clinical trials consultants$500.00
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Collaborate
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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.