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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. Dr. Manish R.
18 years of experience in Clinical Research, Experience in Conducting GCP Audits, Lead Data Management Activities, Manage Medical Writing
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Dr. Rita B.
A health economist with 12+ years of expertise in academia and industry worldwide. Business strategist. Expert in economic modelling and predic...
Dr. Ioannis L.
Accomplished pharmaceutical industry professional with strong background in clinical pharmacology and translational medicine. Experienced in he...
Dr. Meenakshi V.
I have more than eight years of experience in Pharmacovigilance in various roles, including client management and business development, project...
Dr. Srishti N.
"Research isn't complete until it has been communicated." A personal motto that has driven my passion for effective scientific c...
Dr. Arinzechukwu U.
I have over 10+ years experience in medical/content/copywriting and proof-reading/editing as well as over 6+ years experience in cancer researc...
Dr. Sameer Ul H.
As a recent medical graduate eagerly awaiting a residency position, I am excited to bring my knowledge and skills to the field of healthcare. W...
Currently: Group Leader, University of Cambridge, UK Wellcome Trust Cambridge Centre for Global Health Research Field clinical studies of a nov...
My expertise in molecular genetics, genomics, and oncology will allow me to provide valuable support and insight to emerging strategies in pers...
Dr. Jennifer F.
Meticulous academic professional skilled in developing and monitoring various research programs. Bringing a strong foundation of planning, impl...
Dr. Beatriz B.
Dr Beatriz Blanco Rodríguez earned her B. Sc. (Organic Chemistry) and M. Sc. degrees (Advanced Chemistry) at the University of Santiago de...
Dr. Bhuvanesh D.
I directs the development of patient derived organoids (PDO) for rare cancers. My role is to develop the PDO models and help provide laboratory...
Dr. Jayendrakumar P.
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Dr. Meghana D.
Clinical trial protocol & ICD writing , CSR writing , manuscript writing , power point presentations etc.
Dr. Harsh V.
A competent pharma professional with experience in Scientific writing, Regulatory competitive intelligence, DRA, F&D, MSAT and QA. Experie...
Dr. Jeysen Y.
I have 15 years of drug clinical development experience in biotechnology/pharmaceutical organizations of various sizes. My clinical development...
Dr. Patrick W.
I am a Physician Investigator for clinical research trials with more than 20 years of experience in the clinical research industry. I have auth...
Alexander B.
I have 12 years experience, starting as a Lead Coordinator at a clinical research site. Worked in the CRO space in study start-up, as a CRA, Cl...
I am currently completing my residency in orthopaedic surgery at Saint Joseph's University Medical Center in Paterson, NJ. I have spent a ...
I am a certified pharmacist with a postgraduate degree in Pharmacy. I have 4+ years of experience in the Pharmacy domain,...Medical and Health Research, Scientific Writing, and Web Research with the outcome of two International Publications...
Syed Mohsin A.
This is Mohsin, I am a professional Freelancer having extraordinary skills in writing, Marketing & graphic designing. Having 6+ years of ex...
Oyinkansola S.
Hi, Welcome to my profile. Are you looking for a great writer who can commit at least 20 hours or more to work per week? Are looking for can...
Jeremiah O.
I am a highly motivated individual with multi-tasking skills. I effectively communicate with clients to maximize outcomes and ensure they under...
Raheela T.
I am am Australia based writer, who write medical content for Healthcare professionals and consumers. With a keen interest in all things health...
Work with the best clinical trials consultants on demand. Find freelancers for help with clinical trials consulting services, biostatistics, protocol writing and regulatory compliance.
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Kolabtree ensures safety and security of your payments and personal information and project details. Kolabtree’s T&C includes a default confidentiality clause. You can also sign NDAs and custom agreements with freelancers for additional protection.
Post your project and receive quotes from relevant freelancers. You can also search for specific freelancers by expertise and invite them to your project. Discuss your project details with each freelancer before picking the one best expert.
We assure you of a 100% satisfaction guarantee, which means you only pay when you’re 100% satisfied with the work delivered. If you aren’t happy, we will refund 100% of your money.
You can choose to pay either a fixed or an hourly fee based on your scope of work. If you’re not sure how much your project costs, you can discuss with freelancers before arriving at a mutually agreed fee.
Kolabtree's terms and conditions prohibit freelancers from claiming ownership of intellectual property, and as a client, you are able to reinforce the message with additional communication, agreements or contracts.
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No minimum commitment or contract required.
Flexible, secure payments
Pay a fixed or hourly fee. We hold your funds in escrow until you’re ready to pay.
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Hire freelance clinical trials specialists for research$600.00
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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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Clinical trial scientists needed for a mini project$450.00
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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.
