Profile Summary
Sunny S.
Hello, I am Mr. Sunny Omkar Singh. I have over 14+ years of diverse global experience in various facets of Quality Assurance and Regulatory Aff...
Dmytro D.
Search for innovations, especially for new medicines in different areas (neurology, endocrinology, dermatology, OTC etc.). Analysis of existing...
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...
Prangya Paramita J.
Performing End to End Data Management for Start-up, conduct and Close out Phases of Clinical Trials. ✔ Query Management ✔ Data Cleaning Activit...
Kim-Louise R.
Experience in collecting data, data analysis, writing articles, editing articles, formatting articles, publishing articles. Experience in assis...
Nourhan Salloum M.
Bilingual (ENGLISH / FRENCH) Established researcher and multiple grants recipient with peer reviewed publications in both Healthcare and Social...
Bicky M.
With over 15 years of experience in clinical research in different positions, including CRA, Regional Study Manager, Local Study Manager, Study...
Prajjal D.
I am confident in my ability to create innovative solutions to difficult problems, and I take great pride in designing high-quality software ap...
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Njini W.
Regulatory Affairs Specialist with 5+ years of experience
Akshay P.
• Actively involved with patient advocacy organizations to leverage patient participation • Train, supervise, mentor clinical and regul...
Nancy S.
I'm a Clinical Research Lead with 7 years of experience in many therapeutic ares including Oncology(Solid,Hematology and rare) , infectious...
Ganesh S.
Sr Leader 20+ yrs 18+ yrs people management I Operations and Service Delivery !Clinical Data ManagementIT systems and tools | Client & Vend...
Waleed T.
Dr. Waleed Talat stands as a trusted Career Strategist and Multi-certified Resume Writer, boasting a robust track record in resume crafting and...
Haralabos P.
Working as a medical translator for the past 19 years (9 years full time), I have translated a wide range of biomedical documents including med...
Dr Gopirajan J.
Experienced in preparation of documents for clinical trial including methodology/protocol write up and manuscript for publication.
Smadar K.
10 years of post-PhD experience that includes project management, expertise in patient-tailored assay development, best practice human specimen...
Vishal B.
Hi, I'm Vishal Bharti, an Electronics and Communication Engineer and a Bioinformatics Researcher. With a Master of Technology in Biotechnol...
Veer P.
A seasoned IVDR Regulatory Affairs Professional with hands-on experience in Technical Documentation (STED/TD) preparation, Technical file prepa...
I hold a Master of Biotechnology and Business with 15 years industry experience in both laboratory and clinical research. I have extensive expe...
I have had the great honor of earning the Master of Science in Bioscience Regulatory Affairs degree from Johns Hopkins University in the U.S.A;...
Devanshi S.
Creative Writer and Trainer who supports Individuals, Students, and Institutions to explore their hidden potential by overcoming their self-lim...
Sreejith K.
17 years with multiple consulting gigs across North America and Germany. Completed over 100 Projects.Business mind with Project Management,Risk...
David W.
Experience of conducting clinical trials and research projects covering study setup (budgeting, contracts, protocol creation, sourcing vendors,...
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
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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.
