Profile Summary
Dr. Yasmine M.
Medical Doctor (MD) and published medical writer with expertise in clinical research, pharmacovigilance, and evidence-based scientific communic...
Dr. Chand L.
I am a PhD-trained biomedical researcher specializing in liver disease, immunology, and translational research, with extensive experience in ex...
Dr. Symbat B.
My knowledge lies at the intersection of biomedical science, public health, and evidence-based medicine. I am particularly skilled at translat...
Dr. Nashir U.
I am an Assistant Professor in the Department of Radiation Oncology at UT Southwestern Medical Center with over 15 years of experience in cance...
Shaheen Fathima A.
Regulatory documentation either moves a program forward or it doesn't. I make sure it does. I'm a RAC-Drugs certified Regulatory Affai...
Dr. Manjeet S.
Medical doctor (MBBS) with a Master of Surgery (MCh) from the Royal College of Surgeons in Ireland (RCSI), Dublin....Nine peer-reviewed publications across neurosurgery, paediatric neurology, and public health, with a...
Pablo D.
I am a physician and clinical researcher with a distinguished academic background, graduating Summa Cum Laude from the University of Zulia. My ...
Kristen M.
If your research program needs someone who understands the data at a clinical and scientific level — not just a database technician — that is t...
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Nabil S.
I am a clinical researcher with 10+ publications in peer-reviewed international journ...and Q2 journals in immunology My research background spans the full publication cycle — from study design...
Sterling H.
I am a Regulatory, Quality, and R&D professional with 15 years of experience supporting the dietary supplement, food, pharmaceutical, and m...
Dr. Arash B.
Physician-Scientist and Plastic & Aesthetic Surgery specialist with over 10 years...of academic leadership, over 17 years of research, clinical and surgical practice, 27 peer-reviewed publications...
Dr. Muhammad Arfat Y.
I am a seasoned researcher and academic professional with over two decades of experience in pharmaceutical sciences, microbiology, and clinical...
Dr. Omer A.
I am a GMC-registered medical doctor and Emergency Medicine physician with experience in academic medical writing, case report development, man...
Abuzar W.
I am a published peer-reviewed Clinical Pharmacist and Doctoral Researcher with 6 years of active research experience specializing in digital h...
Haya H.
I am a clinical medical student and bilingual medical writer with a specialized focus on clinical research methodology, evidence synthesis, and...
Dr. Rafia H.
I help biotech and academic teams design assays, validate targets, and solve experimental challenges in molecular and cellular biology, immunol...
Dr. Aimilia M.
Experienced Scientific Editor holding a PhD in Chemistry, with 10+ years of experience in research and 5+ years of experience in editing. Area...
Mahadev M.
Mahadev Mukherjee is a pharmaceutical management professional and research content strategist with over 15 years of leadership experience in th...
Dr. Teesha B.
PhD biochemist with 10+ years of experience analyzing complex experimental datasets. I help life sciences companies extract meaningful insights...
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. 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 ...
Faith S.
I am a Clinical and Drug Data Analyst with a B.Sc. in Pharmacology and GCP certification (ICH E6(R2)), specialising in clinical trial data mana...
Dr. Alisa K.
Professor of Anesthesiology and Head of Cardiac ICU with a PhD and over 25 years of clinical and academic experience in cardiovascular and high...
Chinwendu O.
Hi, I'm Chinwe. I’m a biostatistician and epidemiologist with a background in economics, and I work mainly on public health, clinical, and...
Rajnandini P.
I have extensive experience in Regulatory Affairs and Clinical Development, specializing in end-to-end regulatory strategy, clinical study plan...
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.
Keep your project private
Restrict who can see your project and send you proposals. Invite only specific freelancers to view your project.
NDAs and IP protection
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
Post your Project (Free)
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Get Quotes & Choose Experts
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Collaborate
Pre-pay for your project and work with the expert to get your desired output. Keep track of files and conversations in the user-friendly Workspace.
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.