Eswar K.
Having 12+ years experience in clinical research
Bandhan S.
Hi, I'm a researcher, my research focus on • Single-cell Transcriptomics (RNA-seq) • TCGA Omics Data Analysis • Noise/Outlier detection...
Natasha F.
I am currently a cancer researcher at a large pharmaceutical company. My primary scientific background is molecular biology, and I am highly sp...
Mariangela M.
Deep experiece in molecular oncology, NGS, Clinical Research and data management. Autonomy, flexibility, organization and interpersonal skills.
Elena D.
I'm always willing to improve myself, overcoming my limits, and thanks to my love for languages, I've practiced translation working as ...
Rayan T.
👩💼 I am a published scientific researcher. I currently work in academia at King's College London. My areas of expertise ar...
Aasif M.
Clinical Trial Monitoring (4 years) and clinical trial coordination (2 years)
Nisha N.
• Experienced Clinical research professional, with the strong academic foundation of Graduation in Pharmacy and Post-graduation in Biochemical ...
Mamta S.
I have masters in microbiology. Have experience in animal cell culture, molecular biology, microfluidics, teaching and scientific writing.
Nwachukwu J.
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...
Nicole R.
Motivated, customer-focused Project Manager within the Cardiovascular, Metabolic and Critical Care Department who has more than 16 years of exp...
Ama G.
Clinical Data Manager with experience in Clinical Data Management Processes. Competent in Clinical trial end-to-end activities that comprise st...
Prerana D.
A clinical research post-graduate having a vast knowledge over a range of Medical devices consulting services on conformation of 62304:2006 sta...
Andrew B.
Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...
Ismaila Ajayi Y.
As a seasoned medical doctor and...proficient medical writer, I boast over 5 years of expertise, underscored by numerous peer-reviewed publications...
I have an overall experience of three years in healthcare - Pharmacy Sector in developing a first draft in various therapeutic areas, (report W...
Rohan B.
Experience working in Healthcare industry for more than 10 years, providing healthcare industry professionals with solutions when it comes to c...
Paul H.
Experience with all aspects of clinical trial execution, from concept / protocol writing to clinical study report writing. Have worked with a w...
Desa Rae S.
Clinical Operations Director with over 14 years of industry experience in the early (seed) and late-stage biotech sector, as well as the clinic...
Federico F.
Esperienza in data quality e analisi dati in studi clinici.
Ashwini R.
Highly professional and educated with life science, Clinical research knowledge,
Vinod M.
A witness to many Indian and Global Clinical trials! Seasoned Professional with Pharmacy degree and managment from Pune University! Having work...
Regomoditswe R.
A seasoned clinical research professional with extensive knowledge and expertise in a variety of clinical trials, including investigator site m...
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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You will receive detailed proposals directly from Kolabtree. These proposals will include a comprehensive Statement of Work (SOW), project fees, milestones, and deadlines.
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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.
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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.