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Dr. Rodrigo S.
Holds a degree in Physical Education (Licentiate and Bachelor) from the University of Mogi das Cruzes. Earned a Master’s and PhD in Sciences fr...
Dr. Priyakshi G.
PhD in Molecular Medicine (JNU), specializing in host-pathogen interactions, mucosal immunology, and Pseudomonas aeruginosa extracellular vesic...
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Taofik J.
I am a practicing medical doctor with real-word experience in clinical documentation and academic writing. Over time, I have helped colleagues ...
Eduard S.
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Dr. FELIX OKWUDILICHUKWU N.
I am a National Public Health Programme Officer and PhD Researcher in Global Health with over eight years of experience in neglected tropical d...
Dr. Sheila D.
Bilingual (French/English) medical science and regulatory writing specialist with a PhD in Physiology and over a decade of experience spanning ...
Soumyajit M.
Research scientist specialising in ex vivo evaluation of TCR and bispecific immunotherapies using patient-derived cancer organoid models. I des...
Dr. Omar Y.
I am an Anatomist, a holder of MBChB degree, a medical writer, and a data analyst and statistician, currently working as a lecturer at King Sau...
Ambrina K.
Professor of Molecular Medicine and Genetics & Genomics expert with 10+ years of experience spanning clinical variant interpretation, bioin...
Dr. Dominic A.
PhD in Integrative Biomedical Sciences specializing in oncology, PROTAC degraders, DNA damage response, cancer pain neurobiology, and immunolog...
Dr. Cory D.
I am a health data scientist and Postdoctoral Research Fellow at Pennington Biomedical Research Center, Louisiana State University (LSU), worki...
Dr. Amadiva Amos K.
Medical epidemiologist (MBChB, MSc Field Epidemiology) with 11+ years leading national HIV surveillance, strategic information, and monitoring,...
Dr. Hammam O.
I am an HEOR and Market Access Consultant and Researcher with 20 years of experience across pharmaceuticals, healthcare, public health, and ev...
Dr. Vivian T.
I am a board-certified Anatomic and Clinical Pathologist with experience in oncology, molecular diagnostics, medical and scientific affairs, la...
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 ...
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. 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...
Bruno Z.
I am a physician and General Surgery resident at the University Hospital of the Federal University of Santa Catarina (HU-UFSC), Brazil, with cl...
满 李.
Clinical research and clinical data work, not an academic lab post: 5 years in clinical research operations in China - CRA II at a biopharmaceu...
Dr. Francesco R.
I am a clinical researcher and medical writer based in Switzerland, with...experience in clinical research methodology, scientific writing, systematic reviews, biostatistics, and publication...
Navid K.
I am a professional translator, editor, and localization specialist with 15+ years of experience working across Turkish, Persian (Farsi), Azerb...
Dr. Joan M.
I am a physician and PhD researcher specializing in infectious diseases, tuberculosis, tropical medicine and global health, with extensive clin...
Dr. Hanna B.
PhD biochemist with over 40 years of experience in the biotechnology and pharmaceutical industries. I excel at bridging the gap between researc...
Dr. Ana Z.
I am a Radiation Oncologist, Assistant Professor and clinical researcher with experience in clinical radiotherapy, oncology research, clinical ...
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...
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
Discuss your requirements in detail with the experts before accepting the final statement of work from Kolabtree.
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.