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Tarushi P.
Centre for cruelty free testing is a DST-FIST centre by department of science & Technology, Govt. Of india. We are amongst few labs t...
I am working in a medical institute for 9+ years as faculty orthodontist. Currently, I am Associate Professor with responsibility including aca...
Buthaina S.
Experienced Biomedical Scientist/ Healthcare Analytics with a demonstrated history of working in the hospital & health care industry. S...
Dr. Jennifer S.
Medical and science writer with experience in regulatory and academic documents. I have a background in health research and teaching from McMas...
Dr. Amro A.
I am a scientist working in an immuno-oncology biotech and I also have a medical writing consultancy (Amro Biopharma Consulting, Ltd). I have ...
- More than 10 years of experience as a biostatistician - Have worked in many fields (onco-hematology, transplantation, biomarkers, immunology)...
Dr. Indrabahadur S.
Hello everybody, I am Senior Scientist at German Cancer Research Center (DKFZ), Heidelberg, Germany and editorial board member of SM Journa...
GURUDATH G.
Entrepreneur, Design Thinking Master Practitioner & Human-centred Innovation enabler Clinical Research Leader with 8+ years of Project,...
Anjali S.
Performance-driven professional with total 2 decades of rich & extensive experience in Clinical Research & Development, Pharmac...
A highly analytical and creative epidemiologist with experience managing biological data as well as large cohort data using statistical program...
Joshita M.
A passionate researcher, with a Master’s degree in Biomedical Engineering from Carnegie Mellon University (USA), I have 9 years of product deve...
A thorough professional trained in Science, Technical, Engineering, and Medical Research Publishing, I have 3+ years in online publishing. Key...
Alifiya T.
I am a research scientist/medical writer trained in clinical sciences, epidemiology and biostatistics (BDS, MPH, Rutgers University, USA). My p...
Girish H.
An accomplished, versatile, results-oriented clinical research professional with over 16 years of experience in the Pharmaceuticals & M...
I am a PhD Candidate in epidemiology, with expertise in study design, scientific writing, and data analysis (processing large datasets, statist...
Rudra P.
We are a Contract Research Organization (CRO) that focuses on advanced project management, clinical operations, medical writing, statistical an...
Dr. Rushna F.
I would like to describe myself as someone who loves communicating with a larger audience via science communication. My repertoire of work incl...
Dr. Reham M.
Reham has a doctorate in pathology. She has worked as a scientific-medical communicator and writer for 12 years, providing publication planning...
I have a BA in Mathematics and a PhD in Neuroscience. My main research topic is the study of brain plasticity mechanisms enhanced by natural le...
Dr. Renata C.
I am a scientist passionate about communication, especially writing. I am able to easily adapt to new scenarios and opportunities, between basi...
Bharti S.
A strong background in virology, medical microbiology and public health qualifies me to work on COVID-19 projects (factsheets, COVID-19 at home...
Dr. Natassia S.
• Search for biomarkers and causative genes in different Mendelian diseases. • Designed and analyzed GWAS, whole genome sequence, exome sequen...
Dr. Durreshahwar M.
An enthusiastic, self-motivated, adaptive and fast-learning person with broad range of interests in pharmacology, toxicology and breast cancer ...
Dr. Giedrius V.
WHAT I DO: -Preparation of reimbursement dossier for pharmaceuticals, medical devices, services. -Preparation of global value dossier (GVD) -S...
Work with the best clinical trial consultants on demand. Find freelancers for help with clinical trials consulting services, biostatistics, protocol writing and regulatory compliance.
We take several measures to help you work with full confidence and peace of mind.
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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.
