Dennis P.
I’m a highly experienced medical and regulatory editor with 20+ years of experience across clinical, regulatory, scientific, and promotional ma...
Dr. José F.
Physician-scientist and senior clinical research consultant with more than 18 years of international experience across Europe and Africa, worki...
Dr. Angelica C M.
Licensed physician with 3 years of postgraduate clinical and research experience across dermatology, telemedicine, and clinical research. My ba...
Dr. Stephanie L.
Social and clinical epidemiologist with additional training in human behavioural pharmacology and over 10 years of experience in substance use ...
Dr. Oleksiy V.
Experienced clinical research leader with 20 years of experience in clinical trials, including 18 years in Regulatory and Start-Up (RSU). Demon...
Sazib M.
I am a Public Health Specialist, Clinical Research Advisor, and Health Informatics Consultant with over 15 years of experience bridging raw cli...
Gabriel Antonio C.
Systems Engineer and University Professor of Biostatistics with over 11 years of experience in data analysis, statistical modeling, and academi...
Dr. Faith A.
I am a highly skilled and dedicated Professional Writer and Researcher with over 10 years of extensive experience in Medicine, Microbiology, B...
Dr. Monish G.
I am a medical professional with a strong foundation in clinical medicine and a focused interest in clinical research, medical writing, and evi...
Dr. Christine C.
I am a freelance researcher with 25+ years of experience in systematic reviews and evidence synthesis. I have worked for various institutions, ...
Shubham K.
I am an M.Pharm Pharmacology researcher and medical & scientific writer with experience in scientific research, manuscript preparation, lit...
Dr. Sohini B.
I am a PhD-trained environmental microbiologist with postdoctoral research experience at Baylor College of Medicine, specializing in single-cel...
Dr. Sathya S.
I'm a PhD animal scientist with more than three years of postdoctoral research in nutrition, gut microbiology and molecular methods. My wor...
Syed Zohad S.
I am a medical researcher (MBBS) specializing in high-precision evidence synthesis and clinical data analysis....I bridge the gap between raw data and publication-ready results for clinicians, MedTech startups, and...
Immanuel K.
Pharmacist with professional experience across pharmaceutical operations, regulatory compliance, Good Manufacturing Practice (GMP), Good Distri...
Sarah E.
Pharmaceutical regulatory and quality professional with experience in regulatory compliance, quality control, biologics, clinical research, and...
Dr. Faiz Ul A.
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...
Hossein M.
"As a Ph.D. candidate in Medical Microbiology with over 14 years of hands-on clinical laboratory experience, I bridge the gap between trad...
Mohamed M.
Mohamed is a passionate medical intern with a real curiosity for medicine and surgical research. He leads research projects as a main author al...
Isabela C.
I build research-grade B2B contact databases for life-science, healthcare, and medtech organizations. With a background in international health...
Dr. Daniel O.
I am a public health researcher and biostatistician. My work spans epidemiological research, biostatistics, and scient...I have authored and co-authored four peer-reviewed publications in journals including BMC Public Health...
Dr. Yvoone M.
I help researchers, clinicians, and healthcare organizations communicate scientific findings clearly and accurately through medical writing, sc...
Kay G.
Industry consultant/contractor with extensive hands-on experience assisting offshore and domestic clients in bringing molecules to market. Sub...
Dr. Catherine I.
Dr. Catherine E Igben, is a Public Health Consultant, Reproductive Health Researcher, Global Health Educator, and Certified Health Education Sp...
Dr. Mohamed A.
I am an ophthalmologist with 13 years of clinical experience (MBBCh Tanta University 2011, MSc Ophthalmology Menoufia University 2026) currentl...
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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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 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.