Dr. Laila A.
I have been working in medical research since 2009, I had the opportunity to work in the Pharmaceutical and Medical Research center. I worked a...
Dr. Surat S.
I completed my PhD in life sciences from Tata Institute of Fundamental Research (TIFR), India in 2016. My specialization during PhD was cell bi...
Dr. Marjana S.
I am an accomplished research scientist and group leader skilled in design of human and animal studies, in developing and reviewing IRB documen...
Dr. Precious O.
I am experienced in
Dr. Anne M.
I am an epidemiologist (PhD from Utrecht University) and a veterinarian (DVM from Maisons-Alfort Veterinary School). I have been working in vet...
Dr. Hatem D.
Statistician and Data Analyst | Expert in Medical device ,Beauty and pharmaceutical products (Filler -Botox- PRP -etc) , with 15+ years of expe...
Dr. Dr. Nidhi S.
Research areas: Inflammation, Innate Immunity, Pattern recognition receptors, Nucleotide-binding domain, leucine-rich repeat containing recepto...
I am a dynamic scientist and pharmacists with pre-clinical and clinical expertise in neurology, cardiovascular diseases, and oncology with an e...
Formulation and evaluation of Tablets, capsules, emulsion, microspheres, nanoparticles and depot injection. Manuscript writing (Review article,...
Dr. Melisa S.
Experienced researcher with scientific knowledge and expertise in several therapeutic areas, including: metabolic disorders, ophthalmology, gen...
Dr. Ethiene C.
I am a Biomedical Scientist with a multidisciplinary background. I hold a Master's and a Ph.D. in Pharmacology and have worked as a researc...
Dr. Christos P.
An innovative, highly collaborative lifescience leader with extensive experience across all phases of clinical trials development supervision a...
Dr. John N.
[NOT AVAIL ATM] Medical Writer and Grant Writer for 10 years across innovation-intensive research organisations in Australia including the St V...
Dr. Maurizio C.
I am an experienced Ph.D. in biochemistry with a research background and 6+ years of experience in the scientific and medical writing fields. I...
Dr. Rambabu S.
• Identification, assay development and validation of Serum biomarkers and patenting. • Antigen and Antibody design, production and purificatio...
Dr. Karim E.
I hold a Ph.D. in Biological Sciences from the Université Libre de Bruxelles (ULB), Belgium, specializing in gene therapy against cancer. ...
Dr. Suriya S.
✔Prodigy for bringing the change in the Concept of Cord Blood Banking Industry from 2016 ( Preservation and Utilization of Cord Blood units th...
Dr. Elizabeth H.
PhD Candidate with 6+ years of experience in writing and editing academic publications, specializing in oncology and immunology. Expertise in c...
Dr. Juveria U.
I am PhD research scholar with three years of research experience in the field of pharmacology and specialised in clinical research. i have des...
Dr. Saimah R.
A driven professional with background in immunology and a strong inclination towards scientific communication. Demonstrated advanced writing sk...
Dr. Laura B.
As Medical and Life Sciences Business Consultant, it is my ambition to bridge the gap between good science and clinical application to satisfy ...
Dr. Huseyin A.
Forecasting models, ETL process, Mathematical Optimisation, Time-series Analysis, Machine Learning, Data Science, Python, R, Stata, Eviews, SQL...
Dr. Yehia M.
I am an experimental oncoimmunology scientist with expertise in understanding how the immune system works to protect ad eliminate various invad...
Dr. Elena K.
I am a proficient, energetic and detail-oriented doctoral-level researcher with expertise in the fields of neuroscience, psychedelic science, m...
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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Our T&C include a default confidentiality clause that protects your IP and NDA for added protection before disclosing project details.
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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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 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.