Hire Freelance Clinical Trials Specialists: Find Clinical Trial Consulting Services

Eswar K.

Having 12+ years experience in clinical research
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Bachelors
India

Having 12+ years experience in clinical research

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Bandhan S.

Bioinformatician & Statistician | Expert in R & computer aided drug design
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USD 15/hr
M.Sc
Bangladesh

Hi, I'm a researcher, my research focus on • Single-cell Transcriptomics (RNA-seq) • TCGA Omics Data Analysis • Noise/Outlier detection...

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USD 15/hr
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Natasha F.

Industry Researcher | Oncology | Immunology | Microbiology | Scientific Writing | Manuscript Writing | Creative Writing
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USD 89/hr
Masters of Science in Cellular and Molecular Oncology
United States

I am currently a cancer researcher at a large pharmaceutical company. My primary scientific background is molecular biology, and I am highly sp...

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USD 89/hr
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Mariangela M.

Medical Writer, Science Communication, PhD in Experimental and Molecular Oncology
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USD 15/hr
Specializzation in Food Science
Italy

Deep experiece in molecular oncology, NGS, Clinical Research and data management. Autonomy, flexibility, organization and interpersonal skills.

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USD 15/hr
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Elena D.

I'm precise and organized. I'm independent, a fast learner, and an extremely open-minded hard worker.
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USD 8/hr
Liceo Linguistico
Italy

I'm always willing to improve myself, overcoming my limits, and thanks to my love for languages, I've practiced translation working as ...

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USD 8/hr
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Rayan T.

Scientific Researcher | Academic Writer | Digital Health | Mental Health | Digital Mental Health
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USD 50/hr
United Kingdom

👩‍💼 I am a published scientific researcher. I currently work in academia at King's College London. My areas of expertise ar...

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USD 50/hr
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Aasif M.

Clinical Trial Monitoring (4 years) and clinical trial coordination (2 years)
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USD 30/hr
MSC Pharmaceutical Biotchnology
United Kingdom

Clinical Trial Monitoring (4 years) and clinical trial coordination (2 years)

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USD 30/hr
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Nisha N.

Clinical Research Professional with More Than A Decade Of Industry Experience (CRO, Site, And Academic Set-Up)
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USD 60/hr
Master of Science: Biochemical Pharmacology
Australia

• Experienced Clinical research professional, with the strong academic foundation of Graduation in Pharmacy and Post-graduation in Biochemical ...

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USD 60/hr
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Mamta S.

Biomedical researcher with expertise in reproductive biology, clinical research and scientific writing.
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USD 26/hr
Masters of Science - Microbiology
India

I have masters in microbiology. Have experience in animal cell culture, molecular biology, microfluidics, teaching and scientific writing.

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USD 26/hr
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Nwachukwu J.

Data Analyst/ 2 years+ experience/ Copywriter
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USD 10/hr
Bachelor of Medical Laboratory Science
Nigeria

Hi, My name is Joy! Thank you for visiting my profile page! Yes, I am new on Kolabtree, and I don't have 100+ reviews yet as other freelanc...

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USD 10/hr
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Nicole R.

Expert Project Manager Consultant in Clinical Research
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USD 80/hr
Bachelor of Arts
United States

Motivated, customer-focused Project Manager within the Cardiovascular, Metabolic and Critical Care Department who has more than 16 years of exp...

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USD 80/hr
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A D.

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USD 12/hr
Guinea-Bissau

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USD 12/hr
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Ama G.

Freelance Clinical Data Manager & EDC Developer with more than 2 years experience in Clinical Research
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USD 50/hr
MSc.
United Kingdom

Clinical Data Manager with experience in Clinical Data Management Processes. Competent in Clinical trial end-to-end activities that comprise st...

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USD 50/hr
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Prerana D.

Clinical research professional having an extensive knowledge on medical devices CE marking and consulting services.
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USD 10/hr
M.Sc Clinical Research
India

A clinical research post-graduate having a vast knowledge over a range of Medical devices consulting services on conformation of 62304:2006 sta...

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USD 10/hr
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Andrew B.

Medical writer with 4+ years of experience in clinical evaluation
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USD 50/hr
Master of Public Health
United States

Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...

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USD 50/hr
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Viky Gilles Daniel V.

Global Regulatory Affairs Consultant - FDA - Medical Device - Pharma
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USD 150/hr
Global Regulatory Affairs Certification
United States

Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...

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USD 150/hr
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Ismaila Ajayi Y.

Medical Writer with over 5+ years of experience in clinical research and several peer-reviewed publications
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USD 10/hr
MBChB
Nigeria

As a seasoned medical doctor and...proficient medical writer, I boast over 5 years of expertise, underscored by numerous peer-reviewed publications...

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USD 10/hr
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USD 30/hr

I have an overall experience of three years in healthcare - Pharmacy Sector in developing a first draft in various therapeutic areas, (report W...

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USD 30/hr
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Rohan B.

Clinical Research Expert, therapeutics, data analytics, medical records, electronic health records, EDC platform
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Commerce - International Business
India

Experience working in Healthcare industry for more than 10 years, providing healthcare industry professionals with solutions when it comes to c...

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Paul H.

Freelance Clinical Operations Expert with >15 years of clinical research experience / Phase I-IV international trials...
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USD 165/hr
Bachelor of Science in Nursing (BSN) RN
United States

Experience with all aspects of clinical trial execution, from concept / protocol writing to clinical study report writing. Have worked with a w...

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USD 165/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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Federico F.

Clinical Data Manager / Biostatistico freelance | Esperto in SAS, R e SPSS
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USD 10/hr
Data Management per la Ricerca Clinica
Italy

Esperienza in data quality e analisi dati in studi clinici.

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USD 10/hr
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Ashwini R.

Pharmacovigilance, Drug safety, Medical writing, Technical writing
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Masters in Pharmacy
Canada

Highly professional and educated with life science, Clinical research knowledge,

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Vinod M.

Clinical Supplies with Expertise in Blinding/Placebo manufacturing /IWRS/IVRPT /storage and distribution and Cold chain!
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USD 250/hr
B .Pharmacy
India

A witness to many Indian and Global Clinical trials! Seasoned Professional with Pharmacy degree and managment from Pune University! Having work...

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USD 250/hr
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Regomoditswe R.

Clinical Research Project Manager, MPH, Health Economics ( Candidate), PGD Public Health, Registered
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USD 100/hr
Postgraduate Diploma in Public Health
South Africa

A seasoned clinical research professional with extensive knowledge and expertise in a variety of clinical trials, including investigator site m...

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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.

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Contact experts directly

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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Keep track of files and conversations in the user-friendly Workspace.

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Recent Projects
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    $550.00
  • Hiring for clinical trials consultants
    $500.00
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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.