Hire a Freelance Regulatory Affairs Consultant

Nicole R.

Expert Project Manager Consultant in Clinical Research
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USD 80/hr
Bachelor of Arts
United States

Motivated, customer-focused Project Manager within the Cardiovascular, Metabolic and Critical Care Department who has more than 16 years of exp...

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USD 80/hr
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Andrew B.

Medical writer with 4+ years of experience in clinical evaluation
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USD 50/hr
Master of Public Health
United States

Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...

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USD 50/hr
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Viky Gilles Daniel V.

Global Regulatory Affairs Consultant - FDA - Medical Device - Pharma
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USD 150/hr
Global Regulatory Affairs Certification
United States

Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...

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USD 150/hr
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Ninja P.

Regulatory Affairs Professional (Medical Device Consultant)
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USD 39/hr
Regulatory Affairs Medical Device
Canada

An aspirational mind whose main interest is to pursue a career and advance in Regulatory Affairs and Quality Assurance, become part of an este...

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USD 39/hr
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Ismaila Ajayi Y.

Medical Writer with over 5+ years of experience in clinical research and several peer-reviewed publications
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USD 10/hr
MBChB
Nigeria

As a seasoned medical doctor and...proficient medical writer, I boast over 5 years of expertise, underscored by numerous peer-reviewed publications...

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USD 10/hr
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Rohan B.

Clinical Research Expert, therapeutics, data analytics, medical records, electronic health records, EDC platform
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Commerce - International Business
India

Experience working in Healthcare industry for more than 10 years, providing healthcare industry professionals with solutions when it comes to c...

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Tunahan G.

Regulation Expert / Legal Advisor / Ottoman Turkish and Engish Translator
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USD 49/hr
Masters Political Science
Turkey

I do the legal examination of the law proposals given by the deputies, and also prepare the draft bills on the subjects requested by the deput...

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USD 49/hr
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ikra r.

Freelancer Pharmacovigilance Safety specialist with 1 year of hospital experience and 3 years in a well reputed CRO, IND
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USD 40/hr
Masters in Pharmacology
India

1. Interfaces between Company, sponsors, vendors, and other departments in the area of safety and pharmacovigilance. 2. Processes Adverse Eve...

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USD 40/hr
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Regomoditswe R.

Clinical Research Project Manager, MPH, Health Economics ( Candidate), PGD Public Health, Registered
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USD 100/hr
Postgraduate Diploma in Public Health
South Africa

A seasoned clinical research professional with extensive knowledge and expertise in a variety of clinical trials, including investigator site m...

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USD 100/hr
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Minh Tuan T.

High-achieving individual with 4+ years in medical device regulations (EUMDR & FDA) and business process development...
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USD 85/hr
Masters of Science
United States

Regulatory and Clinical Affairs Maintained strong customer relations, providing exceptional on-site technical, clinical, and sales support to o...

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USD 85/hr
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Emil K.

Clinical research specialist with 10 years+ experience of designing and implementing complex clinical trial projects
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USD 75/hr
Master of Medical Science
Greece

Expert in clinical trial design, phase II/III infectious diseases research, LMIC settings, risk analysis, and trial project evaluations

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USD 75/hr
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Mohan M.

Expert Freelance Consultant Standards, Regulatory Affairs & QMS for Medical Device Design & Manufacture
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USD 125/hr
M.E. (Control Systems)
India

Over 35 years of broad experience as Engineering professional…Medical Device Product Regulatory Requirements, Product Design, Project Managemen...

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USD 125/hr
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Sunny S.

Freelance GCP Expert&Auditor| Expert in Clinical Quality Assurance| QA Professional with 14 yrs exp in Clinical Rese...
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USD 55/hr
Bachelor in Law
India

Hello, I am Mr. Sunny Omkar Singh. I have over 14+ years of diverse global experience in various facets of Quality Assurance and Regulatory Aff...

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USD 55/hr
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Janita ..

Freelance content Medical Writer | Expertise in Clinical Research | Pharmacovigilance | Drug Regulatory affairs
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USD 20/hr
Masters in Pharmaceutical Chenistry
Canada

I am a result-oriented professional with 8+ years of experience spanning across academic, research, and industry. I am qualified as a Master of...

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USD 20/hr
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Gretchen C.

Food Labeling and Regulatory Compliance Expert
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USD 175/hr
Bachelor of Art- English
United States

Food Labeling and Regulatory Affairs expert and entrepreneur, founder of CIBUM Associates. With a background in supporting profitable growth fo...

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USD 175/hr
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Mayur B.

Freelance Clinical Study Project Management 6 + years of experience in clinical research
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USD 40/hr
B Pharmacy
India

I am a dedicated and experienced freelancer specializing in Clinical Research. With a passion for Clinical study management, i have 6 + years o...

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USD 40/hr
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MS in Bioscience Regulatory Affairs
India
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USD 25/hr

I have had the great honor of earning the Master of Science in Bioscience Regulatory Affairs degree from Johns Hopkins University in the U.S.A;...

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USD 25/hr
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MSc in Molecular Biology
United Kingdom
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USD 30/hr

A highly motivated Edinburgh-based life sciences professional with a background in academic research (immunology and microbiology), clinical tr...

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USD 30/hr
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Dr Gopirajan J.

Medical writer with 12+ years of experience in clinical research
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USD 15/hr
MSc Public Health
Malaysia

Experienced in preparation of documents for clinical trial including methodology/protocol write up and manuscript for publication.

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USD 15/hr
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Njini W.

Experienced Regulatory Affairs Specialist
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USD 50/hr
Doctor of Pharmacy
Cameroon

Regulatory Affairs Specialist with 5+ years of experience

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USD 50/hr
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Veer P.

IVD Regulatory Affairs Expert | Experience in Technical Documentation Writing for IVDR CE Projects
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USD 30/hr
Master of Pharmacy (M.Pharm) in Pharmaceutical Regulatory Affairs
India

A seasoned IVDR Regulatory Affairs Professional with hands-on experience in Technical Documentation (STED/TD) preparation, Technical file prepa...

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USD 30/hr
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Haralabos P.

Medical/Pharma English into Greek translator with medical background (MD, MSc, PhD, Certified Radiologist)
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USD 35/hr
Certificate in Translation
Greece

Working as a medical translator for the past 19 years (9 years full time), I have translated a wide range of biomedical documents including med...

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USD 35/hr
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Waleed T.

3X Certified Resume Writer (CARW) & CCW ♦ LinkedIn News Collaborator 2024 ♦ Career Coach & Strategist
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USD 20/hr
MBBS
Pakistan

Dr. Waleed Talat stands as a trusted Career Strategist and Multi-certified Resume Writer, boasting a robust track record in resume crafting and...

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USD 20/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.