Profile Summary
Dr. Ahmed E.
An MD with an onging Ph.D. in Healthcare Data Analytics....I have extensive experience within the scope of scientific writing, peer-reviewed publications, advisory...
Dr. Arndt B.
Ph.D. in Molecular Genetics Basic research experience in functional genome analysis, cell cycle and apoptosis Oncology target discovery in phar...
Dr. Jacob V.
MD, Board Eligible American Board of Preventive Medicine PhD in Biomedical Informatics...MS in Biostatistics MPH Previous projects at the hospital where I recently completed my residency in Public...
Dr. Shrinidh J.
I am an agile, performance-driven and critical problem solver scientist with a passion for scientific, pharmaceutical, medical devices, and str...
Dr. Dibato J.
I am a Biostatistician with research experience in diabetes, depression, cardiovascular diseases and clinical trials. Expert skills in Longitu...
Dr. Zsolt Gabor V.
I am an experienced scientific writer in the field of cell and developmental biology. I can contribute to proposed and running research project...
Dr. Eugene S.
Am an academic research and content writer with over 13 years experience and capable of handling various topic and subjects, and delivering hig...
Dr. Jonathan A.
Medical writer with experience in pharmacoeconomics, pharmaceutical policy, health policy, and health services research.
Dr. Nare S.
My science qualification is Ph.D. in pharmaceutical science. My writing qualifications: - Writing in the Sciences Certificate (Stanford Univers...
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. Serena G.
I'm currently a PostDoc Researcher working in the crosstalk between micromiome and tumoral microenvironment in colorectal cancer, combining...
Dr. Alpana M.
A gold medalist dual board-certified dermatologist involved in multiple clinical trails and research work. ...Over 7 years of experience with more than 70 international and national publications....
Dr. Renu T.
I am a medical doctor as well as Master of Philosophy in Neurophysiology. I have experience with writing and editing of book chapters, literatu...
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...
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. Nael A.
Physician with over 12 years of clinical operations experience. Skilled in all aspects of clinical research support including trial management,...
Dr. Xingyu Mark Z.
Freelance Biostatistician & Data Analyst | Expert in SAS, R, STATA, SPSS Medical writer with 8+ years of experience in clinical research
Dr. Timos N.
Research scientist with a PhD in Ophthalmology. Areas of interest also include Scientific Consulting, Health economics, Epidemiology and Medica...
Khalil Ahmad is a Sr Biostatistician and Data Analyst .
I am an Assistant Professor of Statistics, senior Biostatistician/Statistician, and data analyst with an M.Sc., M.Phil., and Ph.D. in Statistic...
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Hi, I'm Denise! I'm a Regulatory Affairs Professional with over 10 years of experience and a Master's Degree in Regulatory Affairs....
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 clause. You can also sign NDAs and custom agreements with freelancers for additional protection.
Post your project and receive quotes from relevant freelancers. You can also search for specific freelancers by expertise and invite them to your project. Discuss your project details with each freelancer before picking the one best expert.
We assure you of a 100% satisfaction guarantee, which means you only pay when you’re 100% satisfied with the work delivered. If you aren’t happy, we will refund 100% of your money.
You can choose to pay either a fixed or an hourly fee based on your scope of work. If you’re not sure how much your project costs, you can discuss with freelancers before arriving at a mutually agreed fee.
Kolabtree's terms and conditions prohibit freelancers from claiming ownership of intellectual property, and as a client, you are able to reinforce the message with additional communication, agreements or contracts.
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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.
