Profile Summary
I am performing as a clinical research consultant since Dec 2017. I had more than a decade of experience in all the domains of clinical researc...
Vandana C.
Experienced leader with a demonstrated history of global project management in the CRO with over 9 yrs of successful experience in Regulatory S...
PROFESSIONAL PROFILE: A Regulatory Affairs/ Quality Operations Professional with thirteen years drug development experience (Pharmaceutical), w...
Damodara rao K.
• Author, manage and review of Company Core data sheet (CCDS), Company core safety information (CCSI) , Module 2 (Clinical and Nonclinical su...
Regulatory professional with 10 years of, experience. More than eight of which within drug regulatory affairs in CDSCO National Drug Regulatory...
Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...
An aspirational mind whose main interest is to pursue a career and advance in Regulatory Affairs and Quality Assurance, become part of an este...
1. Interfaces between Company, sponsors, vendors, and other departments in the area of safety and pharmacovigilance. 2. Processes Adverse Eve...
• Experienced Clinical research professional, with the strong academic foundation of Graduation in Pharmacy and Post-graduation in Biochemical ...
Tunahan G.
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...
Experience working in Healthcare industry for more than 10 years, providing healthcare industry professionals with solutions when it comes to c...
Regomoditswe R.
A seasoned clinical research professional with extensive knowledge and expertise in a variety of clinical trials, including investigator site m...
Gretchen C.
Food Labeling and Regulatory Affairs expert and entrepreneur, founder of CIBUM Associates. With a background in supporting profitable growth fo...
.webp)
I am a result-oriented professional with 8+ years of experience spanning across academic, research, and industry. I am qualified as a Master of...
Over 35 years of broad experience as Engineering professional…Medical Device Product Regulatory Requirements, Product Design, Project Managemen...
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...
Dr Gopirajan J.
Experienced in preparation of documents for clinical trial including methodology/protocol write up and manuscript for publication.
Motivated, customer-focused Project Manager within the Cardiovascular, Metabolic and Critical Care Department who has more than 16 years of exp...
Haralabos P.
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...
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. Sign NDAs 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 clause. You can also sign NDAs and custom agreements with freelancers for additional protection.
Post your project and receive quotes from relevant freelancers. You can also search for specific freelancers by expertise and invite them to your project. Discuss your project details with each freelancer before picking the one best expert.
We assure you of a 100% satisfaction guarantee, which means you only pay when you’re 100% satisfied with the work delivered. If you aren’t happy, we will refund 100% of your money.
You can choose to pay either a fixed or an hourly fee based on your scope of work. If you’re not sure how much your project costs, you can discuss with freelancers before arriving at a mutually agreed fee.
Kolabtree's terms and conditions prohibit freelancers from claiming ownership of intellectual property, and as a client, you are able to reinforce the message with additional communication, agreements or contracts.
Contact experts directly
Speak directly with freelancers and explain your requirements.
100% satisfaction guaranteed
Pay only once work is delivered and you’re happy with it.
No upfront fees
No minimum commitment or contract required.
Flexible, secure payments
Pay a fixed or hourly fee. We hold your funds securely until you’re ready to pay.
-
Hiring for regulatory affairs specialists$550.00
-
Regulatory affairs expert needed$440.00
-
Looking for regulatory affairs consulting services$600.00
Post project (Free)
Post your project publicly for all freelancers to view and send you proposals, or interact with specific freelancers privately.
Choose the best expert
Get bids from relevant experts. Interact freely with them before making a hire.
Collaborate
Share files, make audio/video calls and collaborate with your chosen expert.
Complete project
Verify the project is complete to your satisfaction before paying the expert.
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.
