Dr. Neha G.
Medical writer with a doctorate degree in genetics and experience in preparing and reviewing manuscripts, drug competitive landscapes, clinical...
Dr. Eoghan M.
My combination of science/medical and creative writing expertise make me an ideal partner for producing compelling and accurate content. I have...
Dr. Eric L.
With a strong scientific background, I bring extensive expertise in medical device development's regulatory and quality aspects. As an acco...
Dr. PATRICE ADRIEN S.
After being graduated as medical doctor in Cameroon, I worked as freelance Statistician, digital marketer/salesman for 3 years. As Statistician...
Dr. Jyothsna C.
Skills * Clinical Research * Medical Affairs * Clinical Pharmacology * Clinical Trials * Microsoft Office Suite * Statistical Analysis - SPSS, ...
Dr. Karim E.
I hold a Ph.D. in Biological Sciences from the Université Libre de Bruxelles (ULB), Belgium, specializing in gene therapy against cancer. ...
I have done PhD in molecular oncology. My area of research is mainly use of Oncolytic Vaccinia virus for cancer therapy and to understand the r...
Dr. Shanoor S.
1.5 years of experience Duty Medical Officer and medical writing / scientific writing
Dr. Meenakshi V.
I have more than eight years of experience in Pharmacovigilance in various roles, including client management and business development, project...
Dr. Rita B.
A health economist with 12+ years of expertise in academia and industry worldwide. Business strategist. Expert in economic modelling and predic...
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Dr. Dr. Manish R.
18 years of experience in Clinical Research, Experience in Conducting GCP Audits, Lead Data Management Activities, Manage Medical Writing
Dr. Suresh Kumar K.
I am Dr. Suresh K Karri and I have worked with various Indian and global CRO/Pharma companies. Successfully managed many phase/clinical trials ...
Ana Carolina F.
In order to promote safer and more positive childbirth experiences for women, for the last...nine years I've collaborated in qualitative and quantitative research projects in the areas of: public...
Dr. Thathya V. A.
A dynamic health economic & market access professional with a passion for evidence-based, data-driven medicine: on a mission to improve...
Dr. Bruna B.
Authored and co-authored 18 articles already published/accepted at scientific journals. Assistant Editor at a scientific journal. Member of EM...
Dr. Junaid A.
As an accomplished medical researcher with a strong foundation in public health and microbiology, I bring over a decade of experience in conduc...
Dr. Amber S.
I am a Pharmacist by profession and have done my MPhil and PhD on HEC scholarship. My research projects involves Anti-hypertensive effect usin...
Dr. Danielle D.
Research Psychologist, Scientist, and Statistician 10+ years of experience in scientific research, study design, scientific writing, data anal...
Dr. Srishti N.
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Dr. Ioannis L.
Accomplished pharmaceutical industry professional with strong background in clinical pharmacology and translational medicine. Experienced in he...
Dr. Harri J.
I have 25 years of diverse scientific, managerial and executive experience, including 18 years in pharmaceutical industry. I have managed more ...
Dr. Jan I. Y.
I am a result-oriented, enthusiastic, experienced MD, Internist with a hematology background and good communication, proactive, and innovative ...
Dr. Afsana S.
I'm Dr. Afsana Syed, Pharm.D having an overall experience of 3.5 years in Clinical Pharmacy (1 year) and medical writing (2.5 years). I'...
Dr. Amir E.
At Arizona State University, as a PhD candidate in Biomedical Informatics, I focus on advancing computational methods and data-driven research....
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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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.
Project Management
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Flexible, secure payments
You can choose to pay either a fixed or an hourly fee based on your requirement.
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Clinical trial scientists needed for a mini project$450.00
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Need a clinical trial consultant$500.00
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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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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.