Profile Summary
Horacio A.
Medical researcher specialized in clinical and surgical data analysis. Experienced in managing complex databases using SPSS for statistical inf...
Mona A.
I am a physician-scientist and specializing in neuroimaging, cerebrovascular disease, and AI-based imaging analysis....I have authored over 20 peer-reviewed publications with more than 1000 citations and have presented at...
Vandana B.
Expertise in Clinical Data Integrity & Regulatory Excellence Accomplished professional with over 18 years of experience in Clinical Data ...
Dr. Antoine B.
I am a cognitive neuroscientist and postdoctoral researcher specializing in the neural mechanisms of memory, emotion, and learning....I have a strong publication record of 20+ papers in high-impact journals (e.g., Nature Human Behavior...
Dr. Muhammad Imran K.
I am an experienced Biopharmaceutical Statistician and Data Analyst with over 18 years of expertise in pharmaceutical research, clinical studie...
Dr. Krupa N.
I am a medical writer and scientific visual communicator with a PhD in Molecular Biotechnology and 15 years of translational research experienc...
Dr. ARUN T.
I am a PhD-level researcher and consultant specializing in Yoga, with a dedicated focus on qualitative methodologies and integrative health pro...
Dr. Brian E.
I am a medical doctor, biostatistician,...bioinformatics analyst, and digital health consultant with over a decade of experience in health research, public...
Dr. Elma H.
Elma Hrustemović, DVM, Academic Specialist in Clinical Microbiology and PhD Researcher, is a dedicated scientist at the University of Sarajevo,...
Irina B.
QA compliance, Regulatory Affairs, FDA, MHRA, UKCA/ UK Conformity Assessment (for medical devices post-Brexit) HPRA, WDA, EU medical devices, p...
Dr. Smruti P.
I am an MD Pharmacology resident with expertise in pharmacovigilance, drug safety evaluation, clinical research, and medical writing. My academ...
Dr. Guillermo A B.
As a Physician with an MBA in Healthcare Administration, I bring a unique blend of clinical expertise, research operations, and academic writin...
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Dr. Abdullah O.
I seek opportunities where I can leverage my expertise in aging biology (biogerontology), biochemistry, clinical biochemistry, bioinformatics, ...
Gabriel Antonio C.
Systems Engineer and University Professor of Biostatistics with over 11 years of experience in data analysis, statistical modeling, and academi...
Noah Y.
I am a Lead Geographic Analyst and former NASA Fellow (Duke University MS, William & Mary BS) with over 12 years of experience in geospatia...
Dr. Anurag G.
Are you looking for a medical writer who can navigate complex clinical trial data, draft rigorous protocols, and flawlessly translate that scie...
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...
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.