Profile Summary
Rachid E.
My qualification is an MSc in Biomedical Sciences. I am a Regulatory Affairs Specialist. The primary responsibilities are: - Working with CTD ...
Yasser E.
I have been working in the Clinical Development industry since 2008, I had the opportunity to work in Pharmaceutical and CRO settings covering ...
Xan S.
Fellow Biostatistician, Medical Officer. Fluent in R, STATA and SAS. Generalized Linear models, Linear models, Survival Analysis and Causal Inf...
Judit P.
Scientist with lab experience in protein and antibody engineering, cancer and infectious diseases. Currently doing my PhD in advanced antibody ...
Nitin S.
I am a seasoned professional with extensive expertise in pharmaceutical formulation and cosmetics development. With a robust background in visu...
Noor A.
🔬 Experienced Scientific and Technical Writer 🔍 👋 Hello, I'm Noor Akram, your go-to freelance content writer for al...
Daniel W.
Scientist with extensive management experience, including navigating the operational complexities of cross-functional and multi-PI collaboratio...
Tristen P.
I aspire to generate high-quality evidence-based science that can inform reliable policy decisions. As a research consultant, this translates t...
Misty P.
Design, plan, and execute research projects from start to finish, including document design
Tshetsana S.
I am a dedicated freelance medical writer with a strong background in Pharmacy as a registered Pharmacist, and clinical research and regulatory...
Diana T.
A background of almost 17 years experience in managing and monitoring Clinical Trials, multinational studies (phase II, III and IV ) with study...
Kristin F.
Two Certifications in Data Analytics Currently working on a certificate in IT Automation with Python. Additionally working on a certificate in ...
Viktoria K.
I am an independent clinical research professional with 14 years experiences in the sector. My expert area is clinical trial protocol content r...
Rebecca B.
Systematic reviewer with 9+ years of experience. Produced over 50 high quality systematic reviews and meta-analyses of intervention, diagnostic...
Nouman N.
I have published few original articles and case reports, helped my colleagues in synopsis preparation, dissertation writing and article prepara...
Andreu S.
Statistician with solid background and more than 6 years of experience in Clinical Trials, Research, and Data Science. I am passionate about cl...
Priyanka W.
Experience in following: - Clinical Operations: Clinical Monitoring, Therapeutic Areas, Clinical Trial technologies, QMS Management - People M...
Swapnil V. S.
>15 years of experience in life sciences, R&D, clinical trials and life science entrepreneurship
Sumanta B.
Holding a Master's in Microbiology and a PGDM in Clinical Trials Management, I am an accomplished medical Writer. My journey began with the...
Equipped with formal Biomedical Engineering training, statistics knowledge and programming skills, I'd love to offer my biomedical research...
Christin W.
In the past years of my bachelor's and master's studies, I had the opportunity to acquire a broad knowledge in areas such as biochemist...
Fariha K.
Motivated and hardworking team player with 5+ years of professional and academic experience in research and analytics.
Rahma Mostafa E.
Clinical Project Coordination: Experienced in managing project timelines, resources, and stakeholders to ensure successful clinical trial execu...
Divya J.
Hello! My name is Divya Jagga having medical and scientific writing experience of 6+ years. My academia: • MSc Biomedical Sciences, University...
Alex L.
Alex Lukey is a first year Ph.D. student at UBC’s School of Population and Public Health. Prior to her PhD, she completed her Master of Scien...
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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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.
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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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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.
