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Dr. Fady R.
PharmD with years of experience in the pharmaceutical/biotech space, from leading a multimillion-dollar pharma company to being directly involv...
Dr. SREEDHAR T.
Post Graduate Medical Doctor, MBA in Healthcare and PGdiploma Herbal drug Technology with 15+ years of experience in Clinical Research,Herbal D...
Dr. Tomas W.
I have over 6 years of experience in academic research,...working in world leading laboratories in both the UK and US, with my work leading to 7 first author publications...
Dr. Nabin P.
A clinical scientist with an interest in clinical, socioeconomic research and data analysis & visualization....Have diverse experience in clinical research, science communication, patient involvement and advocacy, public...
Dr. Shruthi E.
Career Objective: To secure a responsible career opportunity to adopt and utilize my public health knowledge and skills while making a signific...
Dr. Seyedeh Mehrnaz A.
I am a medical doctor who is currently employed as a postdoctoral research fellow at the internal medicine department of Mashhad University of ...
Dr. Pollyana C.
I am Biomedical Scientist, a life science researcher with a passion for communicating science concisely and clearly....I have been writing and editing manuscripts for publication in high-quality journals since 2013, and...
Dr. Karl F.
Board-certified pathologist with a specialization on brain diseases and a PhD in neurosciences. Over 10 years of experience in design, executi...
Dr. Gokalp B.
I am an academic person, and also a proficient user of Apple Numbers-Keynote-Pages, Microsoft Office, and statistical analysis program IBM SPSS...
Dr. Lucy L.
Experience working in research and industry settings, both carrying out analyses and consulting on data science strategy.
Dr. Natalia S.
As a former Instructor/Junior Faculty (MD Anderson Cancer Center, Houston, TX, USA), I have a strong knowledge base in cancer biology, and prov...
Dr. Sriti K.
I’m a scientific researcher and a teacher at the academic level. My subject is biotechnology with specialization in the fields of tissue and ce...
Dr. Jabin A.
I am an experienced medical writer in the field of medical communications with medico-marketing skills. I have worked with various deliverables...
Dr. Peter K.
A Statistician with good knowledge and use of statistical softwares for making evidence-based decisions through research.
Dr. Daniel P.
Trained Physician with clinical and 10+ years of practical experience in Market Access and Life Cycle Management of pharmaceutical products in ...
Dr. David M.
✔ Pharmacovigilance Physician, Medical Regulatory Writer, LQPPV, Project Manager, Clinical Trials Regulatory Expert. ✔13+ years professional me...
Dr. Valerio R.
I am an immunologist with strong expertise in microbiota studies. I completed my PhD in Immunology in the laboratory of Prof. Jan Hendrik NIess...
Dr. Maxmilla J.
I am an experienced Medical and Academic Writer with core skills and valuable wealth of experience in diverse subject areas focusing Clinical M...
Dr. Neha G.
Medical writer with a doctorate degree in genetics and experience in preparing and reviewing manuscripts, drug competitive landscapes, clinical...
Dr. Paula P.
- Degree in Pharmaceutical Sciences, Faculty of Pharmacy, University of Porto (2000) - PhD in Analytical Chemistry, Faculty of Pharmacy, Univer...
Dilip B.
Research personnel conducting safe and ethical human research with knowledge of federal regulation, research ethics and GCP guidelines. Skilled...
Dr. Caroline K.
Research experience in developing new sensors to enable biomarker detection | Nanopore sequencing expert | Start-up experience | IP generation
Dr. Carsten S.
– Developing strategic perspectives (Clinical Development Plan, regulatory strategy, market focus) – Implementing strategies into projects (e.g...
Dr. Adam F.
I am passionate about advancing the science and practice of oncology and delivering the best outcomes for patients. My main areas of interest...
Dr. Thathya V. A.
A dynamic health economic & market access professional with a passion for evidence-based, data-driven medicine: on a mission to improve...
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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Restrict who can see your project and send you proposals. Invite only specific freelancers to view your project.
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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.
Contact experts directly
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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Collaborate
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Approve the deliverables once you're satisfied with the job done.
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.
