Hire a Freelance Regulatory Affairs Consultant

Dr. Zaki U.

Expert in Life Sciences Research | Data analysis SPSS | Medical Write-up | RCT & clinical study design | PCR
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USD 30/hr
PhD
Pakistan

17+ Years University Teaching & Research Experience in life sciences, medical / clinical research, Research Projects as Principal Investiga...

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USD 30/hr
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Dr. Shrinidh J.

PhD in Pharmaceutical Science with 15+ years of experience in Pharmaceutical - Clinical - Regulatory- Medical Devices
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USD 150/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 150/hr
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Dr. Mohamed A.

Expert Medical Researcher and Scientific Writer
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USD 20/hr
Bachelor of Medicine, Bachelor of Surgery (MBBS)
Egypt

- I am Mohamed Abdelmonem an expert clinical medical researcher and reviewer. - My research career started three years ago by attending severa...

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USD 20/hr
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Dr. Siddharth C.

Pharmaceutical physician with 20+ years of experience in clinical development, medical writing and pharmacovigilance
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USD 250/hr
Masters
Netherlands

Dr Siddarth Chachad is a pharmaceutical physician with over 20 years of experience in the areas of medical affairs, drug safety and global clin...

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USD 250/hr
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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 a Ph.D. in pharmaceutical science. My writing qualifications: - Writing in the Sciences Certificate (Stanford Unive...

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USD 50/hr
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Dr. Diksha V.

Researcher & Writer with 11+ years of experience in biotechnology, biomedical, bioinformatics and product developmen...
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USD 100/hr
PhD
India

I am a doctorate in life sciences with an experience of over 11 years in the academic and corporate sector. I have managed projects focusing o...

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USD 100/hr
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Dr. Stuart C.

Scientist/Consultant w/R&D & Manufacturing Expertise in Pharmaceutical/Nutraceutical/Food/Cannab...
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USD 150/hr
Ph.D. Pharmaceutical Sciences
United States

Pharmaceutical/Nutraceutical/Food Formulation Scientist with 30+ years of experience developing soft chews, tablet and capsule products, chewab...

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USD 150/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 7 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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Nida A.

Experienced MDR and FDA certified CER/Technical File Writer with 7+ years of experience with multinational industries
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USD 50/hr
Law (LLB Honours)
Pakistan

An experienced clinical research and medical device Technical file writer who has certified on MEDDEV 2.7/1 Rev#4 documentation, EU MDR 2017/74...

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USD 50/hr
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Lisa R.

REGULATORY AFFAIRS - Medical Device - Biotech - Dietary Supplement - Pharma
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USD 200/hr
Certificate of Regulatory Affairs , Dietary Supplements and NHP
Australia

Highly motivated Product Formulation Expert and Regulatory Affairs Expert in the following fields: Medical Devices ,Pharmaceuticals ,Dietary Su...

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USD 200/hr
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Morgan B.

Medical writer with 7+ years of experience in clinical research
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USD 40/hr
MS
United States

Freelance writer with over 7 years in clinical research. I've been involved in medical device trials, drug trials, investigator-initiated s...

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USD 40/hr
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Dr. JORDANA S.

Ph.D. student in pharmaceutical sciences ǀ Pre-clinical/Clinical studies ǀ Innovation ǀ Entrepreneurship ǀ Biotech
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USD 10/hr
M.Sc. Physiological Sciences
Brazil

B.S. in biomedicine, M.S. in physiological sciences, and Ph.D. student in pharmaceutical sciences. I have experience in preclinical and clinica...

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USD 10/hr
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Dr. Alex L.

Former academic, medical devices regulatory affairs consultant, specialising in clinical and performance evaluation.
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Doctor of Philosophy (PhD) Haematopoetic Stem Cell Gene Therapy
United Kingdom

Qualifications: MBiochem Molecular and Cellular Biochemistry, Oxford University PhD Haematopoetic Stem Cell Gene Therapy, University of Manches...

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Dr. Hatem D.

Statistician and Data Analyst | Expert in Medical device ,Beauty and pharmaceutical products (Filler -Botox-PRP-etc)
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USD 250/hr
Masters of Pharmacy
United Arab Emirates

Statistician and Data Analyst | Expert in Medical device ,Beauty and pharmaceutical products (Filler -Botox- PRP -etc) , with 15+ years of expe...

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USD 250/hr
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Dr. Sri Ramulu E.

A highly accomplished biomedical and clinical research expert in drug development
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USD 50/hr
PhD in Biotechnology
India

A highly accomplished biomedical and clinical research expert leveraging extensive medical proficiency to spearhead patient-centric solutions t...

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USD 50/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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Bradley P.

I help world-class teams supercharge and execute their business change programmes without the headaches
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USD 75/hr
Construction Engineering Technology
United Kingdom

I'm Brad Pallister, a data-driven operations and innovation specialist with over 20 years of experience helping businesses achieve growth. ...

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USD 75/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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Damodara rao K.

Regulatory Labeling , medical writer Expert
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USD 20/hr
M.Pharmacy (Pharmacology)
India

• Author, manage and review of Clinical and Non-clinical Overview documents. • Preparation of SOPs, work instructions for writing Global Labe...

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USD 20/hr
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Waqas A.

Regulatory Affairs / Quality Operations Professional (Pharmaceuticals) | RA Freelancer & Consultant
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USD 150/hr
Double Masters
Pakistan

PROFESSIONAL PROFILE: A Regulatory Affairs/ Quality Operations Professional with thirteen years drug development experience (Pharmaceutical), w...

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USD 150/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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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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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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Dr. Nicole S.

Scientific Writer | Medical Communications and Regulatory Affairs
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USD 85/hr
Environmental Health Science, Environmental Toxicology
United States

Doctorate-level Biologist and Medical Writer dedicated to crafting scientifically accurate and high-quality medical communication deliverables ...

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USD 85/hr
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Dr. Nael A.

Physician | Medical Director | Clinical Development | Clinical Operations | Clinal Trials Management | CRO Management
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USD 150/hr
MBA
United States

Certified Principal Investigator and medical director with 12 years of experience in clinical operations and medical affairs. During my career,...

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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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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.

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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.

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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.

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You can choose to pay either a fixed or an hourly fee based on your requirement.

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Get Quotes & Choose Experts

Discuss your requirements in detail with the experts before accepting the final statement of work from Kolabtree.

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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.

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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.