Hire Freelance Clinical Trials Specialists: Find Clinical Trial Consulting Services

Dr. Nuwanthi F.

Medical writing expert!
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USD 70/hr
MBA in Healthcare Administration
Sri Lanka

A Medical doctor, a Member of The European Medical Writers Association (EMWA), medical writer and editor. With more than 7 years of experience,...

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USD 70/hr
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Dr. Nael A.

Physician | Medical Director | Clinical Development | Clinical Operations | Clinal Trials Management | CRO Management
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USD 150/hr
MBA
United States

Certified Principal Investigator and medical director with 12 years of experience in clinical operations and medical affairs. During my career,...

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USD 150/hr
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Dr. Muhammad Hashim G.

Academic Writing | Clinical Trials | Research | Manuscript Writing | SPSS | Proposal Writing | PPT Presentations | SLR
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USD 70/hr
Pulmonary Rehabilitation Certificate
Pakistan

A doctor by profession, a researcher by passion & a staunch believer in the practice of evidence based medicine and clinical research, ...

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USD 70/hr
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Dr. Alpana M.

dermatologist | Freelance medical writer & scientific consultant | SEO writer | Researcher | 85+ publication...
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USD 85/hr
MD (Dermatology, venereology and leprosy)
India

A gold medalist dual board-certified dermatologist involved in multiple clinical trails and research work. ...Over 7 years of experience as a doctor with more than 85 international and national publications....

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USD 85/hr
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Dr. Khalil Ahmad is a Sr Biostatistician and Data Analyst .

Senior Biostatistician and Data Analyst with 15 Years Experience in Data Analytics using R, SPSS, STATA, Python, Jamovi.
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USD 80/hr
MPhil in Statistics
Pakistan

I am an Assistant Professor of Statistics, senior Biostatistician/Statistician, and data analyst with an M.Sc., M.Phil., and Ph.D. in Statistic...

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USD 80/hr
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Dr. Jonathan A.

Medical writer | Adjunct Prof., Faculty of Medicine, University of British Columbia | PhD, UC Berkeley | MBA, London
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USD 150/hr
MBA
United States

Medical writer with experience in pharmacoeconomics, pharmaceutical policy, health policy, and health services research.

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USD 150/hr
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Dr. Jose U.

Scientific Consultant - Imaging Sciences and Data Analysis
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USD 80/hr
PhD
Chile

I am an MRI physicist and imaging scientist with more than 15 years of experience developing imaging biomarkers for the pharmaceutical and medi...

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USD 80/hr
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Denise A.

Experienced Regulatory Affairs Professional
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USD 150/hr
Masters of Science
United States

Hi, I'm Denise! I'm a Regulatory Affairs Professional with over 10 years of experience and a Master's Degree in Regulatory Affairs....

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USD 150/hr
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Dr. Marco C.

Associate Professor in Medicine with 10+ years of experience in medical/scientific writing
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USD 8/hr
Postgraduate Degree in Anesthesiology, Intensive Care, Pain Management
Italy

I am a seasoned medical professional and researcher with expertise in the realm of medical writing. Over the years, my experience has encompass...

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USD 8/hr
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Dr. Rajesh G.

Medical Researcher and Journal Editor | Expert in clinical data analysis
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USD 35/hr
MDS
Nepal

I am working in a medical institute for 9+ years as faculty orthodontist. Currently, I am Associate Professor with responsibility including aca...

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USD 35/hr
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Mohammed O.

Expert in clinical research, Manuscript editor
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USD 80/hr
Master
Ireland

Medical Oncologist

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USD 80/hr
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Danielle K. B.

Clinical Research Professional with Medical Writing experience | Medical Device | Pharmaceutical | Biotechnology
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USD 60/hr
Medical Degree (MD)
United States

I am a Clinical Research professional with 6 years of experience in the various therapeutic areas including Respiratory, Anesthesiology, Critic...

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USD 60/hr
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Joshita M.

Biomedical Engineer, CMU | Product Manager & Medical Writer | Expert in Clinical Research with 9+ years of experienc...
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USD 30/hr
MS - Biomedical Engineering
Netherlands

A passionate researcher, with a Master’s degree in Biomedical Engineering from Carnegie Mellon University (USA), I have 9 years of product deve...

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USD 30/hr
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Rudra P.

Group of Clinical Research Professionals (Project Manager, Biostatisticians, CRAs, Medical Writers, SAS Prgmers)
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USD 70/hr
MS
India

We are a Contract Research Organization (CRO) that focuses on advanced project management, clinical operations, medical writing, statistical an...

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USD 70/hr
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Dr. Hafsa I.

Medical Device Regulation (MDR) - BER - Technical File - CER - ISO13485 - Production manager - SOPs - Design File - GRIN
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USD 35/hr
PhD
Pakistan

Medical Device Production Manager with 5 years of experience in device development - Technical file - Design File - Procurement - Technology De...

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USD 35/hr
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Dr. Adam S.

Scientist and medical writer with experience writing clinical and regulatory documents, publications,
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USD 100/hr
PhD
United States

Experienced scientific and medical writer with expertise in clinical writing (clinical trial protocol, CSR, IB, ICF) and regulatory writing (IN...

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USD 100/hr
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Dr. Sonya D.

Biotech Medical Writing/Stats; Business Strategy and Operations; Data Science; Digital Marketing
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USD 100/hr
PhD
United States

We are a consultancy staffed with several scientists and business experts. ...Our typical scientist has an impressive publication record and PhD + approximately ten years of experience...

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USD 100/hr
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Dr. Adam E.

Freelance drug and medical device Regulatory Affairs consultant | Expert in preclinical and clinical trial design
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USD 100/hr
Doctorate of Philosophy (PhD)
Australia

My research interests are in the design, development and assessment of novel drugs to prevent brain injury in infants and adults.

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USD 100/hr
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Dr. Anurag S.

Pharmaceutical R&D (Formulation development and Analytical) expert, Medical, Science and Research Writing Expert
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USD 10/hr
PHD in Pharmaceutical Science
India

• I am Anurag Sharma, I have completed my post-graduation on pharmaceutical science and PhD in pharmaceutical science with and more than 10yrs ...

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USD 10/hr
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Dr. Pavel O.

AI engineer. Full-stack developer. Physician. Academic.
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USD 50/hr
Doctorate
France

AI engineer. Full-stack developer. Physician. Academic.

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USD 50/hr
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Dr. Milad N.

I am Research Fellow at the University of Oxford.
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USD 200/hr
MSc
United Kingdom

Cardiovascular disease, genetic epidemiology, pharmacogenomics, statistical Modelling, statistical analysis, systematic-review, meta-analysis

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USD 200/hr
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Dr. Angela Patricia F.

Life Sciences PhD | Medical and Scientific Writer with 10+ years of experience in scientific research
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USD 80/hr
Postdoctoral researcher in Pharmacy
Brazil

I'm a PhD-trained medical writer with over a decade of hands-on experience in scientific research encompassing preclinical and clinical tri...

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USD 80/hr
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Dr. Fabiola F.

Clinical Scientist & Medical writer with 8+ of experience in clinical research and scientific communication
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USD 50/hr
PhD
Mexico

Clinical Scientist | Digital Health Entrepreneur translating health innovation projects into clinically implemented realities.

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USD 50/hr
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Dr. JORDANA S.

Ph.D. student in pharmaceutical sciences ǀ Pre-clinical/Clinical studies ǀ Innovation ǀ Entrepreneurship ǀ Biotech
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USD 10/hr
M.Sc. Physiological Sciences
Germany

B.S. in biomedicine, M.S. in physiological sciences, and Ph.D. student in pharmaceutical sciences. I have experience in preclinical and clinica...

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USD 10/hr
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Dr. Laura Marie Z.

PhD Specialist. in Cardiovascular Research and Clinical Trials, helping Pharma and Biotech
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USD 85/hr
PhD Biochemistry
Germany

In the healthcare sector of the pharmaceutical and biotechnology industries, I specialise in cardiovascular research, pre-clinical trial design...

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USD 85/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.

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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.

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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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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.