Hire a Freelance Regulatory Affairs Consultant

Dr. Nare S.

More than 10 years of experience as Regulatory Affairs Specialist, Medical and Scientific Writer, Clinical Trial Consult
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USD 50/hr
PhD in Pharmacy
Armenia

My science qualification is Ph.D. in pharmaceutical science. My writing qualifications: - Writing in the Sciences Certificate (Stanford Univers...

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USD 50/hr
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Dr. Dilip B.

Endorsed by the Royal Academy of Engineering as having exceptional Talent in Biomedical and Medical sciences
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USD 150/hr
PhD, Neuroscience
United Kingdom

I am the holder of highly prestigious Tier 1 Exceptional Talent Visa and endorsed as such by the Royal Academy of Engineering in the fields of ...

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USD 150/hr
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Dr. Nael A.

Physician | Medical Director | Clinical Operations | Clinal Trials Management | CRO Management
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USD 225/hr
MBA
United States

Physician with over 12 years of clinical operations experience. Skilled in all aspects of clinical research support including trial management,...

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USD 225/hr
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Dr. Diksha V.

Scientist & Writer | Expert in life science, cancer biology, drug discovery | Data science/analysis & bioinforma...
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USD 50/hr
PhD
India

I am a doctorate in life sciences with an experience of over 9 years in the academic and corporate sector. I have managed projects focusing on...

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USD 50/hr
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Nida A.

Experienced MDD and MDR certified CER/Technical File Writer with 5+ years of experience with multinational industries
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USD 50/hr
BSC Biomedical Engineering
Pakistan

An experienced clinical research and medical device Technical file writer who has certified on MEDDEV 2.7/1 Rev#4 documentation, EU MDR, ISO-10...

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USD 50/hr
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Farshid S.

Senior food scientist with 15+ years experience in new product development and R&D
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USD 100/hr
Certificate of culinary art
Canada

Food scientist with over 15 years progressive experience in food industry, with emphasis on R&D and Product development, both on the b...

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USD 100/hr
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Madhu S.

Quality and Regulatory Affairs professional | Expert in CE marking, EU MDR 2017, FDA submissions & lead auditor ISO1...
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USD 30/hr
Advanced PG Diploma in CR & Regulatory Affairs (APGDCR-RA)
India

Over 5 years’ experience in Quality and Regulatory Affairs, and technical submissions for a range of medical devices, including Orthopaedics, S...

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USD 30/hr
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Didy Yoga Lucky P.

I am a Pharmacist. I am well versed in pharmaceutical science and cosmetics, whether it is natural or synthetic medicine
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USD 40/hr
Apt
Indonesia

I have experience in in vitro, in vivo, in silico study, analytical of plant extract, and isolation of metabolite. I also have written study to...

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USD 40/hr
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Carmen N.

Freelance Cosmetic Formulation Chemist driven by inclusiveness
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USD 50/hr
Msc in Cosmetic Expertise
France

Biological engineer and cosmetic chemist, i have experience in cosmetic and biotechnology research and development. The cosmetics industry offe...

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USD 50/hr
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Sundeep A.

Medical Device, IVD, QMS, CE Certificate, FDA 510(K), EU MDR, MDSAP, ISO 13485, SaMD, PMS, CER , PMCF, Risk Management
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USD 100/hr
Master of Technology - Quality Management
India

A seasoned professional with a decade of experience, I am a Leader and Speaker in the field of Quality Assurance & Regulatory Affairs, ...

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USD 100/hr
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Libby R.

Regulatory and Dietary Supplement Formulator
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USD 200/hr
Certificate of Regulatory Affairs , Dietary Supplements and NHP
Australia

Regulatory Affairs Expertise in dietary and food supplements in the below markets with over 10 years experience. - Australia - Canada - US - E...

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USD 200/hr
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Dr. Vanshika S.

Medical editor with focus on Neuroscience and Neurology | Science writer and communicator
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USD 60/hr
B.Tech. Biotechnology
India

I am a published neuroscientist with collaborative research work appearing in journals like Oxford Academic's Cerebral Cortex and BMJ's...

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USD 60/hr
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Dr. Hafsa I.

Medical Device Regulation (MDR) - BER - Technical File - CER - ISO13485 - Production manager - SOPs - Design File - GRIN
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USD 35/hr
PhD
Pakistan

Medical Device Production Manager with 5 years of experience in device development - Technical file - Design File - Procurement - Technology De...

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USD 35/hr
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Dr. Fabiola F.

Clinical Scientist & Medical writer with 8+ of experience in clinical research and scientific communication
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USD 50/hr
PhD
Mexico

Clinical Scientist | Digital Health Entrepreneur translating health innovation projects into clinically implemented realities.

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USD 50/hr
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Dr. Dipti S.

ACRP certified clinical research professional with expertise in clinical operations, site management, project management
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USD 40/hr
Master of Science - Psychotherapy & Counselling
Canada

More than 16 years of extensive clinical research experience with expertise in following areas: Clinical Operations - Experienced in conductin...

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USD 40/hr
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Dr. Fady R.

Pharma/Biotech Equity Research Consultant
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USD 750/hr
Master's degree
Switzerland

PharmD with years of experience in the pharmaceutical/biotech space, from leading a multimillion-dollar pharma company to being directly involv...

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USD 750/hr
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Dr. Paula P.

Medical Writer with 15+ years of experience in scientific writing
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USD 75/hr
PhD in Pharmaceutical Sciences
Portugal

- Degree in Pharmaceutical Sciences, Faculty of Pharmacy, University of Porto (2000) - PhD in Analytical Chemistry, Faculty of Pharmacy, Univer...

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USD 75/hr
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Dr. Arinzechukwu U.

Freelance Scientific Writer and Consultant with over 6+ years in cancer research
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USD 100/hr
Molecular Haematology
United Kingdom

I have over 10+ years experience in medical/content/copywriting and proof-reading/editing as well as over 6+ years experience in cancer researc...

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USD 100/hr
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Dr. Ana Luiza C.

Freelance Medical writer, Clinical specialist and Regulatory affairs of Medical Devices, Ph.D. Biological Sciences
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USD 69/hr
MBA Quality Management
Brazil

I have over 8 years of experience in Clinical Research, Regulatory Affairs and Quality Assurance of implantable and electro medical devices in ...

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USD 69/hr
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Dr. Shrinidh J.

PhD in Pharmaceutical Science with 13+ years of experience in Pharmaceutical - Clinical - Regulatory- Medical Devices
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USD 100/hr
Doctor of Philosophy (PhD)
Canada

I am an agile, performance-driven and critical problem solver scientist with a passion for scientific, pharmaceutical, medical devices, and str...

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USD 100/hr
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Manish G.

Cosmetic Chemist I Formulator I Personal Care I Home Care I Project Management
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USD 50/hr

Hi Bindu, I am a hands-on cosmetic chemist with over 26 years of experience in developing wide range of skin care, hair care, make-up product...

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USD 50/hr
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Dr. Sonika V.

Medical Writer and researcher having 10 years of post qualification experience in clinical and epidemiological research.
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USD 70/hr
Diploma in Applied Epidemiology
India

Experienced Medical Writer with a demonstrated history of working in the pharmaceutical industry and research organizations of international re...

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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. 7+ 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. 7+ years in clinical research Studies: I have a b...

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USD 25/hr
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Dr. Hrishikesh G.

Over 30 years of experience commercializing medical devices for large, mid-size and early stage companies.
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USD 125/hr
PhD in Electrical Engineering
United States

Broad hands-on software and hardware development for medical devices such as diagnostic imaging devices (PET, MRI, X-Ray and Ultrasound), blood...

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USD 125/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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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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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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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.