Dr. Luca A.
I am an orthopaedic resident and a research enthusiast with 60+ publications in peer-reviewed journals, 20+ presentations at national and inter...
Dr. Zaki U.
17+ Years University Teaching & Research Experience in life sciences, medical / clinical research, Research Projects as Principal Investiga...
Dr. Jose U.
I am an MRI physicist and imaging scientist with more than 15 years of experience developing imaging biomarkers for the pharmaceutical and medi...
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. Elena V.
I am a highly self-motivated Ph.D. scientist with over 15 years of combined, professional experience in both academia and industry. Due to my y...
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...
- I am Mohamed Abdelmonem an expert clinical medical researcher and reviewer. - My research career started three years ago by attending severa...
Dr. Eugene S.
Am a medical writer with over 15 years experience and capable of handling various topic and subjects, and delivering high quality projects. I a...
Since obtaining my pharmacy license I'm interested in drug therapy, especially in the research and development of drugs with a novel mechan...
Dr. Tomoe G.
I am an experienced scientific consultant providing data analysis services using R and Python. I have trained myself beyond my formal education...
Dr. Lefteris T.
Are you looking for an experienced professional to conduct systematic reviews for your project? Look no further. I am Lefteris Teperikidis, a...
Dr. Siddharth C.
Dr Siddarth Chachad is a pharmaceutical physician with over 20 years of experience in the areas of medical affairs, drug safety and global clin...
Dr. Nare S.
My science qualification is a Ph.D. in pharmaceutical science. My writing qualifications: - Writing in the Sciences Certificate (Stanford Unive...
I was accepted to the MAMF program at Columbia University in 2015 but chose for a variety of reasons to continue the economics doctoral program...
Dr. Scott A.
Medical affairs professional with 6 years of experience in the pharmaceutical and medtech industries and 10 years of experience in academic an...
Driven by a passion for healthcare and innovation, I bring over a decade of expertise in clinical research, project management, and data analys...
I am a research biostatistician with 11+ years of expertise in translational research, which has resulted in 13 publications in high impact pee...
I have a dual-PhD from the Australian Catholic University and the Université d'Avignon, awarded under a Cotutelle....This research program resulted in eight journal publications and two book chapters and was marked by...
Dr. Alpana M.
A gold medalist dual board-certified dermatologist involved in multiple clinical trails and research work. ...Over 7 years of experience as a doctor with more than 85 international and national publications....
Dr. Jonathan A.
Medical writer with experience in pharmacoeconomics, pharmaceutical policy, health policy, and health services research.
Dr. Khalil A.
I'm an Assistant Professor of Statistics, Principal Biostatistician, Machine Learning Expert, and Data Analyst, with an M.Sc., M.Phil., and...
Dr. Vera M.
Providing leadership and strategic direction in Drug/Medical Device Development and Quality assurance to meet the new Industry challenges Leade...
Dr. Muhammad Hashim G.
A doctor by profession, a researcher by passion & a staunch believer in the practice of evidence based medicine and clinical research, ...
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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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.