Profile Summary
Preetha V.
Healthcare professional with lots of academic research experience. One of the research projects on "Comparison of Tranexamic acid and Apr...
Pratiksha S.
● Results-oriented Clinical Research Specialist with expertise in EDC, eSource, and ePRO systems. ● Skilled in creating accurate source form te...
Noor A.
🔬 Experienced Scientific and Technical Writer 🔍 👋 Hello, I'm Noor Akram, your go-to freelance content writer for al...
Dr. Teresia M.
Microbiome and Metagenomics Bioinformatics with 6+ years of experience. Data Scientist and Analyst with 6+ years of experience. Computational ...
Nisha N.
• Experienced Clinical research professional, with the strong academic foundation of Graduation in Pharmacy and Post-graduation in Biochemical ...
Federico F.
Esperienza in data quality e analisi dati in studi clinici.
Mariem R.
I have 15 years of experience in the field of Public Health and Clinical Research in several positions: coordination, monitoring, project man...
Ashwini R.
Highly professional and educated with life science, Clinical research knowledge,
Nitin S.
I am a seasoned professional with extensive expertise in pharmaceutical formulation and cosmetics development. With a robust background in visu...
Desa Rae S.
Clinical Operations Director with over 14 years of industry experience in the early (seed) and late-stage biotech sector, as well as the clinic...
Hannah C.
Accomplished life science researcher with over 5+ years of experience and a proven track record of success in the higher education sector. My b...
Rahma Mostafa E.
Clinical Project Coordination: Experienced in managing project timelines, resources, and stakeholders to ensure successful clinical trial execu...
Emil K.
Expert in clinical trial design, phase II/III infectious diseases research, LMIC settings, risk analysis, and trial project evaluations
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. Hrishikesh G.
Broad hands-on software and hardware development for medical devices such as diagnostic imaging devices (PET, MRI, X-Ray and Ultrasound), blood...
Having been in the science and research for 10 years, I understand the importance of working under strict time lines. Within my career span I h...
Dr. Lefteris T.
Are you looking for an experienced professional to conduct systematic reviews for your project or train you in the process? Look no further. I ...
Dr. Mona Lisa C.
Accomplished scientific writer of winning grant proposals (+$400K) and high-impact papers (including in Nature Methods and Science); Scientific...
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Dr. Anna M.
My name is Dr Anna Patricia McLaughlin, and I'm an academic neuroscientist specialising in mental health and well-being. I completed my PhD...
Dr. Richard David H.
R. David Hayward is a Senior Medical Researcher in the surgery department at Ascension St. John Hospital in Detroit, Michigan. He is an expert ...
Dr. Sanet A.
I provide clinical research and health consulting, medical writing and training services to Pharma, Biotechnology Companies, CROs, NGOs, Founda...
Industry leader with 20+ years of expertise in the clinical trial, drug development space. PhD Biotech, Adv Dip French Literature. Have represe...
Dr. Rosa N.
We are a team of dentists with specialization in bio-statistics. We take up projects on statistical analysis and manuscript preparation. We de...
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. Nicole S.
Doctorate-level Biologist and Medical Writer dedicated to crafting scientifically accurate and high-quality medical communication deliverables ...
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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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.
Project Management
Keep track of files and conversations in the user-friendly Workspace.
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.
