Hire Freelance Clinical Trials Specialists: Find Clinical Trial Consulting Services

Thelma A.

Pharmacist | Pharmaceutical & Medical research and writing
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USD 30/hr
MSc Industrial Pharmaceutics
Canada

A pharmacist with over 6years of experience in the healthcare, medical device and pharmaceutical industry. Invested in carrying out research a...

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USD 30/hr
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Victor L.

Applied Statistician, Biostatistician and Data Analyst. Expert in R, SPSS and scientific writing: 5+ years of experience
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USD 20/hr
Master of Science in Applied Statistics
Kenya

I am a qualified Applied Statistician having pursued MSc. Applied Statistics. I have vast experience in scientific writing and statistical gene...

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USD 20/hr
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Suja G.

Freelance Medical Writer with more than 5 years of experience in Clinical Research, and Health sciences.
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USD 30/hr
MDS Oral Pathology
Canada

Experienced in writing, editing articles, journals, slide decks, and proposals. Competent in protocol reviews, drafting patient brochures, info...

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USD 30/hr
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Carla S. L.

Scientific Writing and Proofreading | Scientific Editing | Consulting | Biomedical research
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USD 40/hr
PhD
Portugal

Ph.D. in Biomedical Sciences with extensive research experience. I offer comprehensive academic support services, including consultation, manus...

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USD 40/hr
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Anna M.

Biostatistican(7 years of experience)&Data scientist with experince in medicine, molecular biology and bioinformatic...
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USD 16/hr
medical doctor
Turkey

Biostatistician | Junior data scientist with experience in data analysis and bioinformatics specified in clinical medicine, molecular biology, ...

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USD 16/hr
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Elsa M.

Clinical Project Manager & QPPV @ ICNAS-Produção
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USD 70/hr
The NEW EudraVigilance System and the electronic reporting of ICSRs in the ISO/ICH E2B(R3) format
Portugal

Excellent team spirit, own initiative, love teamwork, responsibility and capacity to manage conflicts, ability to adapt to different contexts,...

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USD 70/hr
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Tarun P.

Regulatory Expert (Consultant) having 25 years of experience working with Pharma, CRO and Medical Device Industry
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USD 150/hr
MBA
India

Vision-driven executive with over 25 years of demonstrated leadership in the pharmaceuticals industry. Proven track record of driving bold init...

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USD 150/hr
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Keshini S.

Freelance clinical research professional with eight years of experience; BSc. in Medical Bioscience and an MBA
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USD 45/hr
Master of Business Administration
Sri Lanka

From initially coordinating and ultimately supervising Phase IIb and III clinical trial protocols sponsored by pharmaceutical organizations suc...

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USD 45/hr
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Marin L.

10 Years of experience in medical consultation& Writing | Expertise : Infection diseases, women health, ophthalmol...
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USD 150/hr
PhD
Germany

Leading medical strategy in matrix-based global environment and providing scientific and business consultation to a local and global pharmaceut...

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USD 150/hr
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Daniyal S.

Scientific writer | Expert in Medical writer
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USD 15/hr
Bachelor in Pharmacy
India

I'm a hard working, well-skilled article writer I can think critically and writing on my kind of content easily.Reader engagements is the b...

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USD 15/hr
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Brijesh T.

Freelance Academic and Scientific writer. I Research Associate with 2+ years of experience in Clinical Research
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USD 10/hr
Master's in Pharmacology
India

A Clinical Research Professional currently working as a Research Associate with over 3 years of experience in the conduction of end-to-end clin...

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USD 10/hr
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Talita D.

Pharmacist, PhD in Health Sciences | Medical translator 300+ clinical trials documents translated
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USD 50/hr
PhD
Brazil

Pharmacist, PhD in Health Sciences - Expert in pharmacology, immunology and natural products Medical translator 300+ clinical trials documents...

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USD 50/hr
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Gaurav P.

Biomedical Sciences | Inflammation and oxidative stress cell biology | Electrochemical Biosensor | Data Analytics |
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USD 27/hr

Passionate researcher in disseminating the different domain knowledge for interdisciplinary and real-time application through persistent effort...

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USD 27/hr
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Shiraz A.

MSc | Medical Writer | Expert in promotional and CME assets | FDA & PAAB | HCP and Patient | Ad Boards | News Articl...
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USD 95/hr
Masters of Science, Molecular Immunology
Canada

Medical writer with experience in FDA/PAAB compliant promotional assets for HCP, Patient, and DTC audiences. Proficient in MLR submissions and...

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USD 95/hr
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Preetha V.

Freelance medical writer with 15+ years of experience in cardiovascular perfusion and a certified clinical researcher
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USD 45/hr
B.S. Physician Assistant
Canada

Healthcare professional with lots of academic research experience. One of the research projects on "Comparison of Tranexamic acid and Apr...

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USD 45/hr
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Haripriya M.

Microbiology | Botany | Chemistry | Biochemistry. Medical Writer with experience in clinical research
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USD 10/hr
Bachelor of Science
India

B.Sc. in Chemistry, Botany and Microbiology. M.Sc. in Biochemistry

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USD 10/hr
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Nathália B.

Medical/Heatlh copywritting
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USD 10/hr
Graduation
Brazil

Researcher in translational medicine and biomedical with experience in Clinical Research, Translational Research, and Clinical Analyses, I am q...

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USD 10/hr
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Diana R.

Pharmacist | Medical Writer
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Introduction to Health Writing course
Portugal

If you had to choose between quality, timely or compliant work, what would you do? When it come to medical and health-related content, sacrifi...

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Dr. Leya M.

Msc Veterinary Medicine/ Veterinary pathology
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USD 15/hr
Msc in Veterinary Medicine
Namibia

PhD student in Veterinary Pathology focusing on liver diseases .

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USD 15/hr
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Rachel P.

Freelance Clinical Protocol Design and Analyst | MS Translational Pharmacology spec. Clinical Trials
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USD 25/hr
BS Computer and Information Science
United States

Clinical Research Experience: The Ohio State University Wexner Medical Center and The James Comprehensive Cancer Center Masters of Science (The...

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USD 25/hr
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Surya N.

CMC Expert with 20+ years of Regulatory and Formulation experience for USFDA, EMEA, Japan, Canada and ROW Markets
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USD 90/hr
M.Pharm.
India

SME (Subject Master Expert) in the Regulatory Affairs and Compliance Development of Finished Formulations (OSD and Injectable) Scientific Advi...

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USD 90/hr
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Jose A.

Freelance Medical Device professional with over 25 years of experience implementing QMS systems and RA compliance
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USD 175/hr
M.S Clinical Nutrition
United States

Behind every successful medical device registration, there is a team of experts working hard to ensure it meets regulatory requirements. As a Q...

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USD 175/hr
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Sarah B.

Biostatistics consulting services & data analysis by industry experienced Biostatistician (Medical Statistician)
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USD 130/hr
Masters of Biostatistics
United Kingdom

I'm a qualified Biostatistician with several years experience in the design and analysis of clinical studies including clinical trials. Thi...

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USD 130/hr
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Matthew P.

STEM Polymath, STEM Convergence, Computational Complexity, System of Systems Engineering Advisor, Consultant, Visionary
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USD 100/hr
MS- Molecular Medicine, PhD-P4 and Systems Medicine
United States

Matt is a STEM Polymath, Complex Problem Solver, Complexity Engineer, Systems and Network Theorist, Reverse Systems Engineer I. Summary of Prof...

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USD 100/hr
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Neeharika A.

Physician, Oral medicine and head & neck radiology specialist, Medical writer - 9+ years of experience clinical rese...
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USD 20/hr
Introduction to clinical trials
India

Clinical research scientist with expertise in manuscript writing, clinical development, medical and scientific writing

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USD 20/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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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.

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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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Recent Projects
  • Clinical trial scientists needed for a mini project
    $450.00
  • Need a clinical trial consultant
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Get Quotes & Choose Experts

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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.