Profile Summary
Dr. Meghana D.
Clinical trial protocol & ICD writing , CSR writing , manuscript writing , power point presentations etc.
Dr. Jayendrakumar P.
Professional Summary: A. Formulation Development: Vast expertise and experience (10+ Years) in development of Generic (ANDA) and 505(b)(2) p...
Dr. Harsh V.
A competent pharma professional with experience in Scientific writing, Regulatory competitive intelligence, DRA, F&D, MSAT and QA. Experie...
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...
Dr. Jeysen Y.
I have 15 years of drug clinical development experience in biotechnology/pharmaceutical organizations of various sizes. My clinical development...
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. Nupur F.
I have a multidisciplinary background integrated in 5+ years of research experience in molecular biology, yeast genetics and cell biology as we...
Courtney W.
M.S. Health Science (Health Administration- Community Health Education and Promotion); 20+ years of human subject (clinical...trials) and community-based participatory research (behavioral; violence prevention, senior health; public...
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 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...
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...
Puspita G.
Want a challenging career where I can constantly learn new things through experience and to reach higher denomination of success and to explore...
Medical Communications Consultant -Writing Clinical Evaluation Reports (CER) for medical device manufacturers -Preparation of clinical reports ...
This is Dr. Ahmed Taha Abdelsattar - A medical researcher, bio-statistician, and scientific and academic writer. - Published many clinical tria...
SHANTHOSH P.
SPSS,STATA,EPICOLLECT,OpenEpi,Epidata manager. Mentor for MPH trainees
Shahenaz K.
Clinical trial expert who brings years of clinical, as well as content development experience in the pharma/device industry, to any projects I ...
Dr. Akshay D.
Hi, I have done MBBS and MD in Pharmacology. I have a work experience with Indian giant Pharmaceutical companies. I have developed Medicomarket...
A Data Architect specializing in digital information management and media production. I contribute to the production of NLP applications and di...
Nathanael Dore C.
I am a public health expert, epidemiologist, medical translator and a fellow in clinical dentistry. Also I am an interdisciplinary researcher w...
Medcafe S.
We are a group of medical doctors with cumulative 30+ years of experience (as practicing Dr, Academicians and Industry Professionals). 1. 20 y...
MGCTS.ORG is a Contract Research Organisation that works for drug development across the world with major clients in Europe, Asia and Africa. W...
Niranjan A.
A versatile person with an impeccable academic record and an insatiable appetite for knowledge, Mr. Andhalkar began his career in Healthcare In...
Shalitha S.
Molecular biologist with over nine years of experience in the Pharmaceutical & Healthcare industries. Scientific expertise in biomarker stu...
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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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.
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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.
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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.
