Hire Freelance Clinical Trials Specialists: Find Clinical Trial Consulting Services

Andreia L.

Freelance Biomedical Scientist
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USD 50/hr
PhD-Doctoral programme; Medicine (as a degree student)
Portugal

I am a dynamic and self-driven person who can quickly acquire knowledge in new areas and recognize the project needs. I have been taking part i...

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USD 50/hr
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Omar F.

Clinical Research Scientist, Freelance Medical writer, Clinical specialist, Medical writer with 2+ years of experience.
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USD 10/hr
MS in Biochemistry and Molecular Biology
Bangladesh

I am a research scientist/medical writer trained in clinical sciences. I have worked on phase-I of clinical trials in the pharmaceutical indust...

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USD 10/hr
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VISHWESWAR RAO V.

M.Pharmacy, Pharmacology subject expert
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USD 15/hr
B. Pharmacy
India

I have 10+ years experience in teaching pharmacology, clinical pharmacy, pharmacokinetics to B. Pharmacy, M. Pharmacy and Pharm. D students. I ...

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USD 15/hr
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Jessica B.

Global Project Leader in CNS | 10+ years of experience in clinical research | ACRP Certified
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USD 50/hr
Master of Science in Clinical Mental Health Counseling
United States

Global Project Leader in Psychiatry & Neurology. Former Research Scientist in Psychiatry. Experienced ACRP Certified Clinical Research Coor...

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USD 50/hr
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Koushik G.

Freelancing Clinical Data Management from start up to close out study activities
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USD 40/hr
B.Sc Biotechnology
Canada

Total 9+ years experience in clinical data management activities

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USD 40/hr
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Pooja S.

Medical writer with 8+ years experience in Clinical Research
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USD 20/hr
Master's in Clinical Research
India

A highly skilled and dynamic clinical research professional with over 7 years of experience in clinical trials at both national and internation...

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USD 20/hr
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Sebastian J.

Phd in Nutrition and exercise metabolism with more than 20 publications.
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USD 30/hr
PhD
Chile

Teacher of Physical Education, Master in Health and Exercise Sciences and PhD in Nutrition and exercise metabolism. My line of research seeks t...

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USD 30/hr
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Master of Biotechnology and Business
Australia
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USD 30/hr

I hold a Master of Biotechnology and Business with 15 years industry experience in both laboratory and clinical research. I have extensive expe...

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USD 30/hr
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MS in Bioscience Regulatory Affairs
India
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USD 25/hr

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;...

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USD 25/hr
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Sreejith K.

Active LS Blogger,17 years Biotech experience expert in Validation CSV, Veeva Quality Docs, Information Risk Assessment.
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USD 50/hr
Computer Science Engineering
United States

17 years with multiple consulting gigs across North America and Germany. Completed over 100 Projects.Business mind with Project Management,Risk...

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USD 50/hr
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David W.

Experience of conducting clinical trials and research projects from conception through to completion.
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USD 40/hr
PhD
United Kingdom

Experience of conducting clinical trials and research projects covering study setup (budgeting, contracts, protocol creation, sourcing vendors,...

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USD 40/hr
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Devanshi S.

Freelance Clinical Research Professional | ICH- GCP Trainer | Corporate Trainer | Soft Skills Trainer | Content Writer
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USD 30/hr
M.Sc Biotechnology
India

Creative Writer and Trainer who supports Individuals, Students, and Institutions to explore their hidden potential by overcoming their self-lim...

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USD 30/hr
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Smadar K.

Molecular biologist & cancer researcher with 10 years of training and expertise in translational cancer research.
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USD 35/hr
PhD in Biology
Australia

10 years of post-PhD experience that includes project management, expertise in patient-tailored assay development, best practice human specimen...

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USD 35/hr
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Dr Gopirajan J.

Medical writer with 12+ years of experience in clinical research
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USD 15/hr
MSc Public Health
Malaysia

Experienced in preparation of documents for clinical trial including methodology/protocol write up and manuscript for publication.

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USD 15/hr
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Prajjal D.

I am confident in my ability to create innovative solutions to difficult problems.
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USD 250/hr
B.tech
India

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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USD 250/hr
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Akshay P.

Clinical drug development in oncology, hematology and rare disease. Maintain a vast network of KOLs. leverage patient ad
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USD 250/hr
Medical Degree (MD)
United States

• Actively involved with patient advocacy organizations to leverage patient participation • Train, supervise, mentor clinical and regul...

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USD 250/hr
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Bicky M.

Senior Clinical Trial Project Manager and Senior CRA
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USD 60/hr
MSc, Medical Pharmacology,
South Africa

With over 15 years of experience in clinical research in different positions, including CRA, Regional Study Manager, Local Study Manager, Study...

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USD 60/hr
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Prangya Paramita J.

Experience Clinical Data Manager. Handling Clinical Trials of Oncology, Immunology, Metabolic disorders etc.
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USD 50/hr
Masters of Science
India

Performing End to End Data Management for Start-up, conduct and Close out Phases of Clinical Trials. ✔ Query Management ✔ Data Cleaning Activit...

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USD 50/hr
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Hannah C.

A Life science researcher with over 5+ years of experience | Clinical Research, CDM & Drug Regulatory Affairs Certif...
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USD 50/hr
Master of Science - Biotechnology
India

Accomplished life science researcher with over 5+ years of experience and a proven track record of success in the higher education sector. My b...

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USD 50/hr
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Njini W.

Experienced Regulatory Affairs Specialist
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USD 50/hr
Doctor of Pharmacy
Cameroon

Regulatory Affairs Specialist with 5+ years of experience

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USD 50/hr
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Desa Rae S.

Freelance Clinical Consultant & Project Director with 14+ Years of Experience | Immuno-Oncology |
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USD 150/hr
Masters of Science
United States

Clinical Operations Director with over 14 years of industry experience in the early (seed) and late-stage biotech sector, as well as the clinic...

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USD 150/hr
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Haralabos P.

Medical/Pharma English into Greek translator with medical background (MD, MSc, PhD, Certified Radiologist)
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USD 35/hr
Certificate in Translation
Greece

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...

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USD 35/hr
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Waleed T.

3X Certified Resume Writer (CARW) & CCW ♦ LinkedIn News Collaborator 2024 ♦ Career Coach & Strategist
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USD 20/hr
MBBS
Pakistan

Dr. Waleed Talat stands as a trusted Career Strategist and Multi-certified Resume Writer, boasting a robust track record in resume crafting and...

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USD 20/hr
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Ganesh S.

Freelance entrepreneur in clinical drug development, leadership, shared services and delivery
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USD 200/hr
Operations Management
India

Sr Leader 20+ yrs 18+ yrs people management I Operations and Service Delivery !Clinical Data ManagementIT systems and tools | Client & Vend...

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USD 200/hr
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Nancy S.

Managing all Clinical Trial material, Ecosystem enhancement, Clinical trial team training,others find them in my profile
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USD 100/hr
MBA
Egypt

I'm a Clinical Research Lead with 7 years of experience in many therapeutic ares including Oncology(Solid,Hematology and rare) , infectious...

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USD 100/hr
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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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We take several measures to help you work with full confidence and peace of mind.

Keep your project private

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.

Why Kolabtree

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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Post your Project (Free)

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Get Quotes & Choose Experts

Discuss your requirements in detail with the experts before accepting the final statement of work from Kolabtree.

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Collaborate

Pre-pay for your project and work with the expert to get your desired output. Keep track of files and conversations in the user-friendly Workspace.

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Job Done!

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.