Dr. Sanet A.
I provide clinical research and health consulting, medical writing and training services to Pharma, Biotechnology Companies, CROs, NGOs, Founda...
Industry leader with 20+ years of expertise in the clinical trial, drug development space. PhD Biotech, Adv Dip French Literature. Have represe...
Dr. Rosa N.
We are a team of dentists with specialization in bio-statistics. We take up projects on statistical analysis and manuscript preparation. We de...
Dr. William M.
Dr. William McGill is a researcher and biostatistician with wide-ranging experience in the health care and wellness industry. William has signi...
Dr. Nicole S.
Doctorate-level Biologist and Medical Writer dedicated to crafting scientifically accurate and high-quality medical communication deliverables ...
Dr. Serena G.
I'm currently a PostDoc Researcher working in the crosstalk between micromiome and tumoral microenvironment in colorectal cancer, combining...
Dr. Juan J.
Statistical Analysis and Modeling, Time Series Forecasting, Complex Networks, Surveys Analysis, Item Response Models, Physics....Scientific Publications: Over 45 publications, h index=14 Advisor of 7 Magister students and 5 Ph.D....
Dr. Loriana V.
Life Science PhD working at UCL in the field of Stem Cells and Regenerative Medicine. I've been a postdoctoral scientist at Cambridge Unive...
Dr. Edna N.
Experienced Nutritional Scientist within the food and sports industries, with a demonstrated history of working in the food production industry...
Dr. Mohammed F.
I am a surgical fellow who has a wide experience in scientific writing, proofreading, and scientific papers. I have 5+ years of experience in s...
Dr. Serhat Akhanli A.
I have completed my Ph.D. in the Department of Statistical Science at University College London, with two M.S.’s in Statistic from Temple Unive...
I am an R&D Scientist and a former faculty of Biochemistry and Molecular Genetics at the University of Illinois at Chicago I have extensiv...
Dr. Marijn L.
I have close to 20 years of experience in human neuropsychopharmacological research at the Department of Psychiatry and Behavioral Sciences. I ...
A Medical doctor, a Member of The European Medical Writers Association (EMWA), medical writer and editor. With more than 7 years of experience,...
Dr. Renu T.
I have done my pre medical and pre engineering degrees.Now I become perfect on both of these two fields. I am a good lecturar good consultant. ...
Professor Khalid Khan is Distinguished Investigator at the University of Granada, Spain. He has been Professor at the University of Birmingham ...
Dr. Vincent P.
PhD in molecular medicine with a focus on innate immune cells in Alzheimer’s and multiple sclerosis. Project manager for the industry, I not wh...
Dr. Nael A.
Certified Principal Investigator and medical director with 12 years of experience in clinical operations and medical affairs. During my career,...
Dr. Souad M.
I am a hard working and dedicated Clinical Researcher with 20 years of experience in clinical research in the fields of Neurology, Cancer, Card...
Dr. Rabbiya A.
I am an infectious disease researcher working at Universiti Sains Malaysia. My work is aimed at unraveling the complexities of how infectious d...
Dr. Gloria V.
CV • Progressed from fundamental multidisciplinary research (Chemistry, Nanobiotech, Biochemistry) to in vitro Pharmacology (Cell Biology, Targ...
Dr. Shuja T.
A doctor by profession, a researcher by passion and a staunch believer in the practice of evidence-based medicine and clinical research, Dr. Sh...
Dr. VANOJAN M.
I am a medical doctor and a medical writer and editor for the past 8+ years. I have worked with many researchers, surgeons, dermatologists, nep...
Dr. Diksha V.
I am a doctorate in life sciences with an experience of over 11 years in the academic and corporate sector. I have managed projects focusing o...
Dr. Timos N.
Highly motivated executive with a broad experience in clinical research, academia and industry fields. Successfully managed clinical trials pha...
Work with the best clinical trial consultants on demand. Find freelancers for help with clinical trials consulting services, biostatistics, protocol writing and regulatory compliance.
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Kolabtree ensures safety and security of your payments and personal information and project details. Kolabtree’s T&C includes 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 arn’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 in case you want to discuss the fee.
Our T&C include a default confidentiality clause that protects your IP and NDA for added protection.
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You have to approve the deliverables only if quality meets your expectations. If you arn’t happy, we’ll refund your money.
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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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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.