Dr. Sehar S.
I am a PhD graduate in Cellular and Molecular Biology and my area of expertise is Inflammation and Metabolic Diseases. My PhD thesis focused on...
Dr. Prashant P.
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Dr. SMITA S.
I am medical writer having PhD degree. I have experience of writing Clinical Study Reports, Informed Consent Forms, Protocol, Slide decks, Abst...
Global professional, doctoral-level research experience in life sciences. Experienced in scientific writing, ICH-GCP E6 framework, clinical res...
Dr. Dipti S.
More than 16 years of extensive clinical research experience with expertise in following areas: Clinical Operations - Experienced in conductin...
Dr. Paromita R.
My passion to find solutions to complex scientific problems has led to over 15 years of research experience in various fields including structu...
Dr. Dr. Manoj N.
A Medical Director and Business Manager with extensive pharmaceutical industry knowledge, domain expertise in multiple therapy areas and hands ...
Experienced Medical Doctor and Clinical Research Associate with a demonstrated history of working in the medical practice industry. Skilled in ...
Dr. Filonid A.
A highly driven Cardiologist with 6 years of experience in diagnosing and treating patients with acute and chronic medical conditions. Clinical...
Dr. Mudassar Iqbal A.
Pharmacovigilance Expert since last 8 years, Post marketing expert, Medical writing, Clinical safety phase IV study, Skin care expert
Dr. Vera Bin San C.
Are you looking for a medical writer who can prepare regulatory submissions for an investigational medicinal product (IMP), e.g. clinical resea...
Dr. Gabriella G.
Goal-oriented biomedical research with more than 10 years experience and demonstrated achievement in managing clinical/translational research p...
Dr. Aissulu I.
CT: oncology, infections, gastro, gynecology, diabetis
Dr. Dayene C.
Experience with: Clinical Trials Phase I-IV, Lung Therapy and Toxicology, Respiratory Disease (including COVID-19), Cell Therapy (Stem Cells), ...
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Dr. Christo K.
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Dr. Nitin M.
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Dr. Erika P.
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Dr. Masood K.
Pharmacology, clinical truals ,article writting ,drug uses and abuses
My background includes nine years of translational research experience and four years of clinical research management and proposal management e...
Dr. Arun K.
I have around twenty years of experience in medical research with sound knowledge in statistical methodology. My varied research experience inc...
Born and raised in Toronto (Canada), I have developed a passion for interdisciplinary biomedical sciences, with interests ranging from biostati...
Dr. Dr. M. Waqee-ur- R.
My area of interest is Materials science (theoretical and experimental study). I worked on the synthesis and characterization of high temperatu...
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...
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 is the place to go for professional help. Work was done promptly and efficiently. I would definitely seek the service again in my future projects
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The quality and quantity of accessible experts on Kolabtree is priceless.
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Clinical trial scientists needed for a mini project$450.00
Need a clinical trial consultant$500.00
Freelance clinical trials consulting services needed$500.00
Looking for a clinical trials advisor$550.00
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.