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Hire a Freelance Regulatory Affairs Consultant

Dr. Anushikha D.

Dentist and and MPH with 6+ years in evidence-based medical and scientific writing, research, and medical communication
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USD 42/hr
Master of Public Health
India

I am a dentist and public health professional with a Master's in Public Health from All India Institute of Medical Sciences (AIIMS), Rishik...

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USD 42/hr
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Dr. Allan A.

Biochemist/chemistry & Academician with over 15+ years of experience
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USD 60/hr
PhD
United States

Dr. Allan Ayella is Founder, and Chief Scientific Officer for ADEK BioPharma LLC, a consulting firm in chemistry/biochemistry research, food te...

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USD 60/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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Dr. Jatinder H.

MD & Public Health Expert | Published Author | Specialist in Evidence Synthesis, Policy Reports &
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USD 55/hr
Medical Degree (MD)
United Kingdom

Award-winning medical doctor and public health expert with a distinguished record of translating complex science into powerful, authoritative w...

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USD 55/hr
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Dr. Guillermo A B.

Physician & MBA | Clinical Research, Trial Operations, and Scientific Writing from Concept to Publication
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USD 85/hr
MBA Healthcare Administration
United States

As a Physician with an MBA in Healthcare Administration, I bring a unique blend of clinical expertise, research operations, and academic writin...

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USD 85/hr
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Irina B.

Pharma & Medical Device HPRA & EU Regulatory Affairs Expert | WDA/GDP Compliance | QP/RP Services – 15+ Years Ex...
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USD 400/hr
MSc. Oncology Research and experimemtal design
Ireland

QA compliance, Regulatory Affairs, FDA, MHRA, UKCA/ UK Conformity Assessment (for medical devices post-Brexit) HPRA, WDA, EU medical devices, p...

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USD 400/hr
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Dr. Amoit W.

Clinical Research & Pharmacology Expert | Clinical Trials | Regulatory Compliance
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USD 20/hr
Bachelor of Pharmacy
Kenya

I am a Research Pharmacist at Kenya Medical Research Institute (KEMRI) with hands-on experience in designing, reviewing, and managing clinical ...

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USD 20/hr
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Dr. Oleksiy V.

Clinical research expert with 20 years of experience in clinical trials, including 18 years in Regulatory and Start-up
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USD 500/hr
Medical Degree (MD)
United States

Experienced clinical research leader with 20 years of experience in clinical trials, including 18 years in Regulatory and Start-Up (RSU). Demon...

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USD 500/hr
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Dr. Fernando T.

PhD in Pharmacology | Expert in Medical Translation, Scientific and Clinical Writing (EN<>PT)
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USD 30/hr
PhD in Pharmacology
Spain

🎓 PhD-level Pharmacologist with over 6 years of experience in preclinical research, pharmacology, and biomedical sciences with scientif...

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USD 30/hr
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Sania S.

Clinical Researcher, Medical Writer, Data Analyst
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USD 20/hr
Masters of Science
Pakistan

"Provide Manuscript/review Article in 7 days.” Impact-driven Clinical Researcher and Data Analyst with 9+ years’ experience leading multi-...

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USD 20/hr
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Dr. Ts. Muhamad Afiq Faisal Y.

Business Development | Researcher (Pharmacology, Infectious & Neurodegenerative Diseases) | Lecturer | Marketer
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USD 20/hr
Doctor of Philosophy (Ph.D)
Malaysia

I am a results-oriented professional with a PhD in Pharmacology and Toxicology, complemented by industry experience in international business d...

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USD 20/hr
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Dr. Robbie C.

Computational neuroscientist with virtual healthcare industry experience.
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USD 150/hr
PhD | Neuroscience
United States

AI/ML Engineer and Data Scientist with a decade of experience driving digital health innovation from startup inception to large-scale data solu...

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USD 150/hr
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Naoki M.

Clinical Pharmacist with +15 years | Regulatory Affairs Manager, Cosmetics | 250+ Cosmetics Approved | RP,CPSR,PIF pro
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USD 24/hr
Bachelor of Pharmaceutical Sciences
Japan

I am a licensed clinical pharmacist with over 15 years of experience in Japan's healthcare and cosmetics regulatory sectors. Currently serv...

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USD 24/hr
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Dr. Amin H.

PhD Biomedical Engineer | Expert in Scientific Manuscripts, Literature Reviews & Medical Device Regulatory Documents
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USD 80/hr
Ph.D
Belgium

I never planned to spend my career listening to the heart, but that’s where science led me. For the past decade, I’ve been obsessed with one q...

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USD 80/hr
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Dr. Akbar Z.

Regulatory Affairs Specialist (EMA/EU) | Pharmacovigilance | Scientific & Medical Writing
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USD 35/hr
PhD | Neuroscience
Estonia

I am a Regulatory Affairs Specialist and dQPPV with expertise in EMA and EU submissions, pharmacovigilance, and compliance documentation. I cur...

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USD 35/hr
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Renu J.

Clinical Trial Manager & PhD Scientist | Protocols • Literature Reviews • Regulatory Writing • Molecular Biology Exp...
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USD 120/hr
DPhil (PhD) Epigenetics
Canada

I am a PhD-trained scientist in Epigenetics (University of Toronto) with a Master’s in Molecular Biology and extensive experience working acros...

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USD 120/hr
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Manju Shree S.

Expert Medical Writer | MSc Pharmacology & Infectious Disease Control | 5+ Years Academic & Research Expertise
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USD 49/hr
Infectious disease control
Sweden

With over seven years of expertise in pharmacology and infectious disease control, I bring a strong blend of academic research and hands-on tea...

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USD 49/hr
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Dr. Sardar Mohammed J.

Senior CMC & Analytical Chemistry Expert | HPLC/LC-MS, Impurities, Stability | PhD Peptide Chemist & Patent Hold...
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USD 55/hr
PhD
United States

I am a PhD-trained Analytical & Peptide Chemist with 20+ years of experience supporting global pharmaceutical, herbal, cosmetic, nutraceuti...

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USD 55/hr
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Dr. Anurag G.

Scientific Content Strategist (PharmD) |Clinical Trial & Regulatory Content | Manuscripts, Protocols, CSRs, Presenta...
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USD 45/hr
Doctor of Pharmacy (Pharm.D.)
India

As a clinical research professional with advanced Pharm.D. training, I bridge the critical gap...between complex scientific data and the clear, persuasive content required for regulatory approval, publication...

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USD 45/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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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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Post your Project (Free)

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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.