Profile Summary
Dr. Mona Lisa C.
Accomplished scientific writer of winning grant proposals (+$400K) and high-impact papers (including in Nature Methods and Science); Scientific...
Vast experience in formal writing in various healthcare domains. I started my journey as a writer in a firm and shortly found my area of intere...
Juan Manuel F.
Clinical Project Manager, Research and Development Technical Expert and University Lecturer. 7+ years in clinical research Studies: I have a b...
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...
SHANTHOSH P.
SPSS,STATA,EPICOLLECT,OpenEpi,Epidata manager. Mentor for MPH trainees
This is Dr. Ahmed Taha Abdelsattar - A medical researcher, bio-statistician, and scientific and academic writer. - Published many clinical tria...
Dr. Sanet A.
I provide clinical research and health consulting, medical writing and training services to Pharma, Biotechnology Companies, CROs, NGOs, Founda...
Niranjan A.
A versatile person with an impeccable academic record and an insatiable appetite for knowledge, Mr. Andhalkar began his career in Healthcare In...
Doctor of Medicine (postgraduate in Ayurveda) with vast experience in pharmaceutical medical affairs. Expertise in medico-marketing, medical co...
A pharmacist with over 6years of experience in the healthcare, medical device and pharmaceutical industry. Invested in carrying out research a...
Vision-driven executive with over 25 years of demonstrated leadership in the pharmaceuticals industry. Proven track record of driving bold init...
Passionate researcher in disseminating the different domain knowledge for interdisciplinary and real-time application through persistent effort...
Haripriya M.
B.Sc. in Chemistry, Botany and Microbiology. M.Sc. in Biochemistry
Jessica B.
Global Project Leader in Psychiatry & Neurology. Former Research Scientist in Psychiatry. Experienced ACRP Certified Clinical Research Coor...
Krishna K.
Clinical Project Management and Medical Writing professional with 11+ years of experience in bio study activities including project planning, m...
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...
I'm always willing to improve myself, overcoming my limits, and thanks to my love for languages, I've practiced translation working as ...
I have an overall experience of three years in healthcare - Pharmacy Sector in developing a first draft in various therapeutic areas, (report W...
Koushik G.
Total 9+ years experience in clinical data management activities
Scientist with lab experience in protein and antibody engineering, cancer and infectious diseases. Currently doing my PhD in advanced antibody ...
Federico F.
Esperienza in data quality e analisi dati in studi clinici.
I am Alaa Elshanbary, a medical researcher focusing on primary (Clinical trials- Cohort- Cross-sectional- Case reports) and secondary research ...
A) Skilled in Microsoft Office (Word, Excel, PowerPoint); EndNote; Origin Pro Graphing and Analysis software B) Regular literature review thro...
Work with the best clinical trials 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 clause. You can also sign NDAs and custom agreements with freelancers for additional protection.
Post your project and receive quotes from relevant freelancers. You can also search for specific freelancers by expertise and invite them to your project. Discuss your project details with each freelancer before picking the one best expert.
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You can choose to pay either a fixed or an hourly fee based on your scope of work. If you’re not sure how much your project costs, you can discuss with freelancers before arriving at a mutually agreed fee.
Kolabtree's terms and conditions prohibit freelancers from claiming ownership of intellectual property, and as a client, you are able to reinforce the message with additional communication, agreements or contracts.
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No minimum commitment or contract required.
Flexible, secure payments
Pay a fixed or hourly fee. We hold your funds in escrow until you’re ready to pay.
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Hire freelance clinical trials specialists for research$600.00
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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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Clinical trial scientists needed for a mini project$450.00
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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.
