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Hire a Freelance Regulatory Affairs Consultant

Dr. Ali H.

MD | Epidemiologist | Advanced Biostatistician (R) | SEER, NHANES, MIMIC, Causal Inference & Survival Analysis Speci...
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USD 50/hr
Doctor of Medicine
Lebanon

I’m an MD and clinical epidemiologist specializing in advanced biostatistics, large-scale health datasets, and publication-ready analysis. I wo...

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USD 50/hr
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Marko K.

Pharmacist & Regulatory Affairs Consultant | Expertise in Clinical Research & Medical Writing
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USD 80/hr
MBA
Germany

Pharmacist | Regulatory Affairs & Clinical Compliance Specialist Experienced pharmacist with a background in GDP logistics, medical device...

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USD 80/hr
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Gevorg Y.

Independent Clinical Research & Evidence Synthesis Consultant | CRA • TMF Oversight • Systematic Reviews
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USD 60/hr
Certified Clinical Research Associate
Canada

I’m an independent Evidence Synthesis and Clinical Research Consultant with over 15 years of combined academic and clinical research experience...

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USD 60/hr
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Dr. Michael A.

Harvard-Trained | MD & MPH | Expert in Medical Research, Clinical Trials, Academic Consulting & Healthcare Innov...
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USD 40/hr
MPH
United States

I am a Harvard-trained clinical researcher and medical writer (MD, MPH) with over 10+ years of experience in academic publishing, clinical tria...

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USD 40/hr
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Nisha V.

Medical & Pharmaceutical Writer | Expert in Cosmetics, Nanotechnology & Regulatory Content | Assistant Professor
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USD 25/hr
Masters in Pharmacy
India

I am a Pharmaceutical Researcher and Assistant Professor with 8+ years of experience in pharmaceutics, formulation development, cosmetics innov...

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USD 25/hr
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Dr. Muhammad Arfat Y.

Microbiologist, Pharmacist and Clinical Researcher Specialised in Pharmaceutical Research & Clinical Trials
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USD 30/hr
PhD
Pakistan

I am a seasoned researcher and academic professional with over two decades of experience in pharmaceutical sciences, microbiology, and clinical...

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USD 30/hr
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Sterling H.

Regulatory, Quality & R&D Consultant | Dietary Supplements, Food & Pharma | 21 CFR 111/117, GMP, Product Dev...
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USD 150/hr
Master of Science in Quality Assurance
United States

I am a Regulatory, Quality, and R&D professional with 15 years of experience supporting the dietary supplement, food, pharmaceutical, and m...

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USD 150/hr
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Dr. Aimilia M.

Scientific Editor
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USD 50/hr
Chemistry PhD
Greece

Experienced Scientific Editor holding a PhD in Chemistry, with 10+ years of experience in research and 5+ years of experience in editing. Area...

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USD 50/hr
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Lisa L.

Statistician and programmer in HEOR and RWD (HTA submission) with 6+ years professional experience | R and SQL user
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USD 150/hr
Masters of Science in Statistics
Canada

Meta analyses; NMA; MAIC; surrogate endpoint analyses; report writing; R and SQL coding

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USD 150/hr
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Sasha S.

Expert Medical Writer & Data Analyst | 15+ Years Publishing in Top Journals | Academic & Technical Writing | Pro...
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USD 30/hr
Masters of Science
United States

I am a highly accomplished Researcher, Medical Writer, Data Analyst, and Product Developer with over 15 years of expertise in academic writing,...

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USD 30/hr
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Leloko N.

I TRANCRIBE, PROOFREAD, COMPILE AND ANALYSE DATA
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USD 10/hr
BACHELOR OF PHARMACY (HONS)
Botswana

I am Pharmacist with about 10 years of experience in clinical setting.

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USD 10/hr
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Dr. Nazanin S.

Regulatory Affairs Consultant | 18+ Years in Pharma | Ex-Merck | EMEA & MENA Expert
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USD 75/hr
PhD (Chemistry)
Iran

I am a pharmacist and senior Regulatory Affairs expert with over 18 years of experience in the pharmaceutical industry, including 9 years in a ...

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USD 75/hr
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Jackie G.

PhD Researcher | Qual & Quant Methods | Nursing, Healthcare & Clinical Research | ML Applications
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MSc (A) Nursing
Canada

I am a bilingual PhD candidate in Experimental Medicine at McGill University with a strong interdisciplinary background in nursing, neuroscienc...

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Sangita M.

Pharmacologist | Medical Writer | Molecular Docking & Toxicology Expert | Holistic Health Consultant
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USD 35/hr
M.S Pharmacology and Toxicology
India

I am a research professional with an M.S. (Pharm) in Pharmacology & Toxicology from the National Institute of Pharmaceutical Education and ...

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USD 35/hr
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Athalia M.

Medical Writer & Clinical Documentation Expert | MSc Clinical Trials | DE/EN | GCP/SOPs
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USD 85/hr
Master of Science (MSc)
Israel

I’m a remote-based Medical Writer and Clinical Documentation Specialist with over 15 years of experience in pharmaceutical development, working...

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USD 85/hr
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Dr. DAWN S.

Principal Consultant US & UK based Life Science Expert
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USD 160/hr
Post doc
United Kingdom

Independent life sciences consultant with 20+ years of experience spanning medical writing, clinical development, market and competitive intell...

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USD 160/hr
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Dr. Joseph B.

MD-PhD Global Health Economist | Cost-Effectiveness & HTA Specialist
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USD 150/hr
MBA
United States

Dr Joseph B. Babigumira is a physician-economist whose two-decade career blends frontline clinical insight with advanced economic evaluation, h...

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USD 150/hr
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Dr. Patricia D.

PhD Pharmacist | Scientific & Regulatory Writer | Pharmaceutical R&D Expert
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USD 25/hr
Doctorate
Brazil

I am a Pharmacist with a PhD in Sciences Applied to Health Products (UFF) and a Master’s degree in Pharmaceutical Sciences (UFRJ), combining ov...

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USD 25/hr
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Lakshmi Rohini T.

Microbiology & Life Sciences Freelancer | Clinical Research, Literature Review & Scientific Editing, Data Analys...
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USD 15/hr
MSc Microbiology
India

Postgraduate in Microbiology from the Central University of Tamil Nadu with an advanced diploma in Clinical Research. I have hands-on research ...

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USD 15/hr
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Dr. Shifa J.

Regulatory Affairs and Scientific Research professional
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USD 30/hr
Graduate certificate
Canada

Regulatory Affairs and Scientific Research professional with 6+ years of combined experience in biotech, academia, and government. Skilled in r...

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USD 30/hr
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Antonio L.

Medical Writer and Editor
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USD 20/hr
Bachelor of Nursing
Philippines

I hold a Doctor of Medicine degree and have over 10 years of professional experience in medical writing for various healthcare, scientific, and...

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USD 20/hr
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Dr. Krishnaa U.

Clinical Pharmacologist | Clinical Research & Drug Development Expert | ICH-GCP, USFDA, EMA Compliance | Medical &am...
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USD 90/hr
PhD
India

I am a Clinical Pharmacologist and Clinical Research Professional with 13+ years of global experience across pharmaceutical industry, CRO opera...

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USD 90/hr
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Dr. Jan S.

Scientfic Expert | Critical Reader and Writer | PK/PD Specialist | Experiment and Product Designer | Regulatory Affairs
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USD 60/hr
Doctor of Philosophy - PhD
Austria

🚀 Your Go-To Scientific Consultant for Mission-Critical Projects 🚀 Need an expert who can not only understand complex science ...

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USD 60/hr
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Renya M.

Regulatory Analyst with proven expertise in IRB submissions and compliance, binder QA/QI, and site start up processes
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USD 50/hr
Master of Public Health
United States

Regulatory Analyst with proven expertise in IRB submissions and compliance oversight, binder QA/QI, FDA inspection preparation, regulatory docu...

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USD 50/hr
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Vishalbhai N.

Good Clinical Practice (GCP) & CSV Consultant/Freelancer & auditor with 18 years of experience
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USD 15/hr
MBA
India

Certified Quality Assurance professional (RQAP–GCP) with an M.Pharm in Quality Assurance (Gold Medalist) and an MBA in Project Management, offe...

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USD 15/hr
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Work with freelance regulatory affairs consultants for product development support. Medical devices, pharmaceuticals, biologics, biosimilars, and more. Get help with FDA submissions, regulatory affairs consulting services, MDR compliance, and more.

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Confidentiality Assured

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.

NDAs and IP protection

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.

Why Kolabtree

Contact experts directly

Speak directly with freelancers and explain your requirements.

100% satisfaction guaranteed

You have to approve the deliverables only if quality meets your expectations. If you arn’t happy, we’ll refund your money.

Project Management

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

Flexible, secure payments

You can choose to pay either a fixed or an hourly fee based on your requirement.

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How it works View full page
1

Post your Project (Free)

Your project details are safe, secure and visible only to logged-in users.

2

Get Quotes & Choose Experts

Discuss your requirements in detail with the experts before accepting the final statement of work from Kolabtree.

3

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.

4

Job Done!

Approve the deliverables once you're satisfied with the job done.

What is a Regulatory Affairs Consultant?

A regulatory affairs consultant helps companies obtain the necessary accreditation and permissions involved in the manufacture and distribution of drugs, medical devices and related products. 

What Does a Freelance Regulatory Affairs Consultant Do?

A regulatory affairs specialist uses scientific research, knowledge and analysis to ensure the safety and efficacy of various products before they hit the market. This includes medical devices, healthcare products, pharmaceuticals etc.

Through this product check, a regulatory affairs specialist ensures that the product meets the various regulations mandated by local and international federations, including safety and compliance requirements.

Qualifications for a Regulatory Affairs Specialist

Regulatory affairs consultants typically hold a bachelors or masters degree in the niche field they operate in, such as biochemistry or pharmaceuticals. They also have a thorough understanding of the various regulations and compliance requirements involved in the product they’re being consulted for.

In addition, regulatory affairs consulting service experts also have,

  • A good understanding and anticipation of evolving regulatory rules that might impact the business and product
  • Ability to document and explain the rules, protocols and procedures to all the employees and stakeholders.
  • Analytical skills and ability to maintain audits, as well as marketing and legal documentation, for the purposes of assessing compliance.

Benefits of Hiring Freelance Regulatory Affairs Specialists

Regulatory affairs specialists typically consult on-demand, as and when the business needs review and compliance for new products. This provides great business value for the company, as they can turn to freelance regulatory consultants for,

Recommending a course of action to help the company achieve compliance and eventually go to market

Help the company prepare the necessary paperwork and ensure approval from the necessary government bodies.

This also gives the company the opportunity to hire cost-effective regulatory affairs consultants who can be hired as and when the demand arises. Freelance consultants typically can be hired from anywhere in the world, enabling the companies to pick and choose the best expert regardless of location.

Cost of Hiring a Regulatory Affairs Expert

The cost involved in hiring a regulatory affairs expert varies according to the duration of the project, and the exact niche of consulting required.

On Kolabtree, you can hire a regulatory affairs consultant from $40/hour up to $150/hour, whilst senior regulatory affairs specialists charge around $225-300/hour. 

How to Post a Project to Hire Freelance Regulatory Affairs Consultants

Before posting a project, take into account the following,

  • How long you need to hire a regulatory expert for
  • The exact niche and expertise you need
  • The budget you’re willing to spend

Now, post a project on Kolabtree based on these criteria, which will help you attract relevant proposals from your project. Then, you can browse through the various regulatory affairs consulting services experts, review their educational and work credentials, and find one that best suits your requirements.