Hire a Freelance Regulatory Affairs Consultant

Assia H.

PhD Biomedical Scientist & Medical Writer | Clinical Trial Documentation | Multilingual: English, German, French, Ar...
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USD 45/hr
Doctoral Program
Germany

I hold a PhD in Inflammation and Cancer Therapy, with over 6 years of research experience and a strong publication record. My work has focused ...

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USD 45/hr
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Maham S.

Pharmacist | Metabolomics & ML Researcher | Regulatory Affairs Specialist | Scientific & Medical Writing Expert
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USD 40/hr
Masters of Pharmacy (Medical Sciences)
Korea, South

Pharmacist with a Master’s degree in Medicinal Science from Chung-Ang University, South Korea, and over three years of research experience. Spe...

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USD 40/hr
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Dr. Muhammad Akbar R.

Multidisciplinary Health Scientist | Peer-Reviewed Publications | Epidemiology | Maternal Health | Spor...
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USD 15/hr
PHD in Public Health
Pakistan

Dedicated Public Health Researcher and Healthcare Professional with extensive experience in epidemiology, maternal and child health, and optome...

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USD 15/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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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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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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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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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. Annunziata C.

Biomedical scientist: 15+y experience in basic, translational, and clinical studies, in a plethora of contexts
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USD 100/hr
II level Master degree
United States

I have worked on a wide variety of fields and on a plethora of pathological and physiological contexts, from basic to translation and then pre-...

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USD 100/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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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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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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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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Our T&C include a default confidentiality clause that protects your IP and NDA for added protection.

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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.