Hire a Freelance Regulatory Affairs Consultant

Dr. Evita A.

Medical Writer/Regulatory Affairs/Project Manager
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USD 210/hr
Masters degree in Biomedical Science
United States

A clinical research scientific writer with clinical medical, CSR. and regulatory CER expertise in MEDDEV 2.7/1 rev4 documentation, EU MDR and F...

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USD 210/hr
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Dr. Rita B.

Health Economist, Data Analyst, HTA, Systematic Review and Meta-Analysis, Publications Support | 12+
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USD 150/hr
PhD
Belgium

A health economist with 12+ years of expertise in academia and industry worldwide. Business strategist. Expert in economic modelling and predic...

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USD 150/hr
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Dr. Eric L.

Regulatory Affairs & Quality Assurance Consultant (Medical Devices)
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USD 90/hr
Ph.D. Molecular Biology
Spain

With a strong scientific background, I bring extensive expertise in medical device development's regulatory and quality aspects. As an acco...

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USD 90/hr
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Dr. Ioannis L.

Pharmaceutical Industry professional with 5+ years of experience in drug development
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USD 160/hr
PhD Biopharmaceutics & Pharmacokinetics
Switzerland

Accomplished pharmaceutical industry professional with strong background in clinical pharmacology and translational medicine. Experienced in he...

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USD 160/hr
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Dr. Karim E.

Molecular biology, immunology, vaccinology, virology, gene- cell therapy, clinical and non-clinical research
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Ph.D. Sciences
Belgium

I hold a Ph.D. in Biological Sciences from the Université Libre de Bruxelles (ULB), Belgium, specializing in gene therapy against cancer. ...

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Dr. Maria Paula S.

I have ove18 years of experience in food science and new product development, as well as a strong commitment to research
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USD 100/hr
PhD in Industrial Chemistry
Argentina

I have a Bachelor degree in Food Science and Technology and PhD in Industrial Chemistry from the University of Buenos Aires. Highlights of my b...

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USD 100/hr
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Dr. Harsh V.

Medical/Scientific/Regulatory/Newsletter/CMC/Dossier/Research/Review/Thesis/Protocol/Report/Article writing & editin...
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USD 30/hr
PhD
India

A competent pharma professional with experience in Scientific writing, Regulatory competitive intelligence, DRA, F&D, MSAT and QA. Experie...

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USD 30/hr
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Dr. Elizabeth H.

Experienced Scientific Writer | Specializing in Clinical Protocols, Regulatory Documents, & Research Publica...
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USD 30/hr
BS, Biochemistry
United States

PhD Candidate with 6+ years of experience in writing and editing academic publications, specializing in oncology and immunology. Expertise in c...

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USD 30/hr
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Dr. Ewa M.

Competition and regulation PhD economist with 15+ years experience
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USD 250/hr
PhD
Netherlands

I am an economist specialising in competition and regulation issues. I obtained a PhD in industrial organisation from Erasmus University in Rot...

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USD 250/hr
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Reno G.

Food Scientist | Chef Developer| Labeling expert | Professional Cheese-maker | 15 years of experience
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USD 70/hr
MSc in Food Innovation and Product Design - specialized in Culinary Innovation, Marketing & Consumer Behaviour, and Business Development
Ireland

Passionate Food Scientist and Chef Developer with an MSc in Food Innovation and Product Design, BSc in Food Science and Technology (Valedictori...

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USD 70/hr
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Denise A.

Medical Device Global Quality and Regulatory Expert
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Bachelor's of Science and Associates of Business Administration
United States

I am an experienced Quality and Regulatory professional with over 25 years in the medical device manufacturing industry. I have worked with Cla...

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Manish G.

Cosmetic Chemist I Formulator I Personal Care I Home Care I Project Management
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USD 60/hr

I am a hands-on cosmetic chemist with over 26 years of experience in developing wide range of skin care, hair care, make-up products such as l...

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USD 60/hr
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Sid P.

Expertise in all types of cosmetics products, helping clients in each stage of cosmetic product development
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USD 50/hr
Masters in Cosmetic Technology
India

I provide services in each stage of cosmetic product life cycle. I am having 8+ years of experience in Cosmetic Product Development in India an...

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USD 50/hr
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Selina B.

Experienced medical writer
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USD 70/hr
Doctorate of Medicine (MD)
United States

Medical Communications Consultant -Writing Clinical Evaluation Reports (CER) for medical device manufacturers -Preparation of clinical reports ...

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USD 70/hr
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Juan Manuel F.

Clinical Project Manager, Research and Develop. Technical Expert and University Lecturer. 9+ years in clinical research
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USD 25/hr
Master in Project Management
Spain

Clinical Project Manager, Research and Development Technical Expert and University Lecturer. 9+ years in clinical research Studies: I have a b...

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USD 25/hr
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Thariq A.

Regulatory Affairs having 3+ experience in field.
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USD 20/hr
Master of Pharnmacy
India

I am having experience in Medical writing, Regulatory affairs, Pharmacovigliance, i am able to do dossiers work, Licence work.

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USD 20/hr
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Melanie S.

Freelance Biomedical Data Analyst | Expert in Bioinformatics and Pharmaceutical Sciences
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USD 40/hr
Professional Science Masters in Bioinformatics (Life Sciences Concentration)
Philippines

A pharmacist by profession with a degree in Professional Science Masters in Bioinformatics and completed coursework in MS Pharmacology. Worked ...

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USD 40/hr
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Richa K.

Freelance FSSAI Regulatory Expert for Foods, Beverages and Food supplements/Nutraceuticals with 14+ years experience
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USD 50/hr
Master of Science
India

An experienced Regulatory Affairs professional with significant industry know-how across food supplements/nutraceuticals/foods products. I am a...

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USD 50/hr
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Viqar A.

Medical Device RAQA & NPD Specialist | ISO 13485:2016 Certified Lead Auditor
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USD 50/hr
M. Tech (Nanoscience and Technology)
India

Nanotechnology and Medical Device enthusiast with experience in New Product Development, Regulatory Affairs and Quality Management System. Work...

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USD 50/hr
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Pradip F.

R & D Expert, Scientific Advisor/Strategist/consultant with >20 years of experience in Lifesciences and Healthcar...
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USD 30/hr
M.Sc.
India

I am managing R & D project for in-vitro diagnostics, in-vitro drug screening, medical device, and vaccine development. I look into all as...

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USD 30/hr
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Sindhu K.

Specialized as GMP Coordinator, QA & Regulatory Professional; have over 18+ years of experience
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USD 75/hr
Bachelor in Pharmacy
Canada

EXPERTISE  18+ years of experience working with companies across Asia, Australia and Canada  Quality Assurance, Compliance & GMP Coor...

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USD 75/hr
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Juan M. C.

Medical Device quality & regulatory expert with + 33 years experience in the industry
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USD 150/hr
Global Leadership
Spain

Juan M. Campos is a Medical Device professional with + 33 years of continued industry experience. His main areas of expertise include Quality A...

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USD 150/hr
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Lini S.

Regulatory Affairs Expert with 20 Years Experience (Regulatory and Scientific Writing Services)
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USD 90/hr
MSc Pharmaceutical Chemistry
India

Specialities - Well-versed in EU Registration procedures (DC/MR, CP and nationals). - CMC Dossier Development & writing - Regulatory St...

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USD 90/hr
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Kishor U.

A pharmaceutical professional with hands on experience in regulatory writing for wide range of product portfolio.
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USD 25/hr
Pharmacology
India

I have a Master's degree in pharmacology with about 7 years of experience in both CMC and the Clinical domains of regulatory affairs. I am ...

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USD 25/hr
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Rita S.

Formulation Chemist | 25+ years | Ingredient Specialist | Reg & Compliance | Training & Education | Marketing Co...
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USD 150/hr
Diploma
Australia

Development in Personal Care & Home Care Science. University Qualified with Bachelor in Science, Cosmetic Science. Skills in - Research In...

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USD 150/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.

Recent Projects
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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.