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RANJIT T.
I am an MD internal medicine consultant. i am also ECFMG certified with an OET B grade in clinical medicine. I have done medical content writin...
Dr Priyanka G.
Doctor by profession, writer by passion with 7 years of experience in academic writing, research writing, study design preparation, manuscript...
Tadesse Waktola G.
I am Biomedical Engineer with over 6 years of experience in health systems, healthcare technology, medical devices and pharmaceticals. I am hig...
Michael G.
I am a medical writer with an MD and training in rehabilitation medicine with extensive experience within that field, as well as a Masters in B...
Kelechi A.
I have experience in quantitative, qualitative and systematic research and I can analyse data using spss. Have experience in health research an...
Christine W.
For the sake of brevity, I will just say I have a wide range of professional and personal experiences that have given me enough knowledge and p...
Sourabh D.
Expertise in the development of active pharmaceuticals ingredients, chemicals, Intermediates. Versatile experience in the scale-up of the resea...
John S.
Healthcare executive with particular experience in healthcare quality improvement and bioethics.
Jasmine P.
Medical graduate ,currently finishing post graduation in pharmacology from a respected institution in South India. Presently has completed thre...
Beenish I.
Hello. I am Dr.Beenish Iqbal.A medical doctor by profession and a writer by passion. Since last year, I have been working on Upwork and have co...
I possess more than 7 years of progressive experience in the medical writing field. My professional history includes positions such as Medical ...
Mansi G.
I am working as a Senior Content Writer. I do write SEO friendly, Keywords based, Plagiarism-free, grammatically accurate, unique and creative,...
Shilpa R.
I am a dentist with a vast experience of 17 years. I am majorly into smile designing and root canals. I do some freelancing and am now looking ...
Angela C.
I specialize in science paper editing and proofreading. I especially enjoy helping clients whose first language is not English improve the flow...
Yassine A.
I graduated medical school, where I studied medicine in both english and french. I rotated through different wards with a focus on physciatry, ...
Karen G.
SUMMARY: Versatile medical laboratory scientist (medical technologist) with 20+ years’ experience in a laboratory setting. An aspiring copywrit...
Fernanda C.
Bacharelor's in Physiotherapy (2020) , with more than 4 years of experience in health research,
Rokia S.
I am a fresh medical graduate, Menoufia Medical School, Egypt. I am a scientific committee member at the Student Research Program (SRP), as a r...
HM Zeeshan R.
I'm working as a freelance research writer in molecular biology, biotechnology, microbiology, genetics, genomics, nutrition, health care, e...
Lenka S.
Epidemiologist/ Public Health Specialist with international working experience. I have three years of experience working in an Agile environmen...
Flavia F.
Passionate about science with strong background on research. Motivated to develop myself as a strong science professional and engage in new opp...
siddhartha k.
Completed Orthopedics Surgery form a renowned medical college.
Amy B.
I work full-time at a university healthcare centre. Offering freelance consultations to academic researchers and innovative medical companies t...
Experienced entrepreneur with a demonstrated history of working in the biotechnology industry. Skilled in Recombinant DNA, Biotechnology, Cell ...
Lais C.
I executed: project 1: Brazil and Mexico, conversations between cultures; Project 2: Teaching Genetics in Schools project 3: sustainable entrep...
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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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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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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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.