Profile Summary
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Karima B.
I am a Regulatory Affairs Senior Specialist with over 15 years of experience in the pharmaceutical industry, including 12 years in generic drug...
Dr. Pamela S.
I’m a PhD-trained clinical research consultant with over 10 years of experience managing regulated trials in both academic and sponsor environm...
Fernanda C.
I hold a degree in Biotechnology, a Master’s in Pharmaceutical Sciences, and a specialization in Regulatory Affairs. With over five years of ex...
Dr. Diane N.
Experienced Biomedical Engineer | Extracellular Vesicles, Drug Delivery Systems, AI/ML for Translational Research I am a PhD-trained biomedical...
Dr. Adrienne D.
I am a clinical researcher, biomedical engineer and academic leader with over 20 years of experience in strategic research development, quantit...
Vrushali P.
I’m a highly motivated and certified Clinical Research Professional with hands-on experience in clinical trial operations, regulatory submissio...
Maham S.
Pharmacist with a Master’s degree in Medicinal Science from Chung-Ang University, South Korea, and over three years of research experience. Spe...
Muhammad F.
Pharmaceutical marketing specialist with nearly seven years of diverse experience spanning brand management, product launches, and cross-functi...
Kristen D.
Innovative executive in clinical operations and regulatory affairs with successful experience in start-ups, hospital & CROs, private equity...
Dr. Lokesh Kumar B.
I am Lokesh Kumar Boopathi, a Doctor of Pharmacy and Regulatory Affairs Specialist with hands-on experience in regulatory documentation, medica...
Dr. Muhammad Akbar R.
Dedicated Public Health Researcher and Healthcare Professional with extensive experience in epidemiology, maternal and child health, and optome...
Dr. Raminder S.
Friendly and highly qualified Senior Scientist with 15+ years of international experience in molecular biology, genetics, tissue engineering, a...
Sydney D. L.
Data scientist and strategic project manager with 7+ years combining clinical research expertise, statistical analysis, and machine learning ap...
Dr. Asha J.
I am a Regulatory & Bioanalytical Scientist with over 12 years of experience in PK/PD studies, Immunogenicity (ELISA, MSD, ADA, NAb assays)...
Sunita V.
• Regulatory Documentation – CTD/eCTD, ANDA/NDA filing, Regulatory submissions (US, EU, ROW) • Quality Assurance – GM...
Dr. Sean V.
I’m a PhD-level scientist ready to help researchers, clinicians, and biotech companies turn complex scientific findings into clear, compelling ...
Shaheen Fathima A.
I am a Regulatory Affairs and Clinical Research professional with expertise spanning drug development, compliance strategy, and scientific docu...
Gokul P.
An accomplished leader with 14 years of extensive experience in clinical development and medical affairs. Expertise encompasses managing large ...
Dr. Shahanara V.
MBBS, MPH, DGH (RCP UK) with over 6 years of experience in obstetrics & gynecology, clinical trials, and public health. Skilled in medical ...
Dr. Kathryn O.
Scientist with over 10 years of proven research experience in preclinical and clinical settings working independently to design, optimize and e...
Victoria B.
I am a clinical research professional with 6+ years of experience in oncology, hematology, and sickle cell research. I hold a Master’s in Biolo...
Dr. UDAY KUMAR K.
I am a Ph.D. holder with specialized expertise in toxicology risk assessment for the pharmaceutical industry, focusing on permitted daily expos...
Dr. Amardeep Singh S.
Innovative R&D Research Scientist with advanced Six Sigma certification and proven expertise in statistical data analysis using industry-st...
Deepak D.
Highly motivated Regulatory Affairs professional with strong expertise in U.S. FDA 510(k) submissions, Indian import licensing (CDSCO), ISO 134...
William K.
I am a life sciences researcher and scientific consultant with over 10 years of experience leading translational research projects across micro...
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.
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.
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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Hiring for regulatory affairs specialists$550.00
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Regulatory affairs expert needed$440.00
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Looking for regulatory affairs consulting services$600.00
Post your Project (Free)
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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.
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.
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.