Profile Summary
Tarun P.
Vision-driven executive with over 25 years of demonstrated leadership in the pharmaceuticals industry. Proven track record of driving bold init...
Simona S.
Coordinated multiple number of regulatory and pharmacovigilance projects such as finalizing regulatory strategy roadmap, technical review of co...
Talita D.
Pharmacist, PhD in Health Sciences - Expert in pharmacology, immunology and natural products Medical translator 300+ clinical trials documents...
SIMONA S.
Deliver wide range of regulatory affairs services, including CTD audit dossier, proof reading, translations, variations, document compilation n...
Surya N.
SME (Subject Master Expert) in the Regulatory Affairs and Compliance Development of Finished Formulations (OSD and Injectable) Scientific Advi...
Jose A.
Behind every successful medical device registration, there is a team of experts working hard to ensure it meets regulatory requirements. As a Q...
Damodara rao K.
• Author, manage and review of Company Core data sheet (CCDS), Company core safety information (CCSI) , Module 2 (Clinical and Nonclinical su...
Mayur B.
I am a dedicated and experienced freelancer specializing in Clinical Research. With a passion for Clinical study management, i have 6 + years o...
Priyanka W.
Experience in following: - Clinical Operations: Clinical Monitoring, Therapeutic Areas, Clinical Trial technologies, QMS Management - People M...
Motivated, self-driven entrepreneur, consultant to regulatory affairs and QC/writing departments within the medical, biotech and pharmaceutica...
Kamal P.
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...
Waqas A.
PROFESSIONAL PROFILE: A Regulatory Affairs/ Quality Operations Professional with thirteen years drug development experience (Pharmaceutical), w...
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...
Mariangela M.
Deep experiece in molecular oncology, NGS, Clinical Research and data management. Autonomy, flexibility, organization and interpersonal skills.
Elena D.
I'm always willing to improve myself, overcoming my limits, and thanks to my love for languages, I've practiced translation working as ...
Neeti S.
Regulatory professional with 10 years of, experience. More than eight of which within drug regulatory affairs in CDSCO National Drug Regulatory...
Aasif M.
Clinical Trial Monitoring (4 years) and clinical trial coordination (2 years)
Nicole R.
Motivated, customer-focused Project Manager within the Cardiovascular, Metabolic and Critical Care Department who has more than 16 years of exp...
Andrew B.
Technical writer with 3 years’ experience executing clinical-regulatory documentation and demonstrated knowledge of EU MDR, clinical evaluation...
Viky Gilles Daniel V.
Guru providing regulatory affairs services to the medical device / medtech, biotech, and pharmaceutical industries. Qualification supported by ...
Ninja P.
An aspirational mind whose main interest is to pursue a career and advance in Regulatory Affairs and Quality Assurance, become part of an este...
Ismaila Ajayi Y.
As a seasoned medical doctor and...proficient medical writer, I boast over 5 years of expertise, underscored by numerous peer-reviewed publications...
ikra r.
1. Interfaces between Company, sponsors, vendors, and other departments in the area of safety and pharmacovigilance. 2. Processes Adverse Eve...
Nisha N.
• 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...
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.
