Top Freelance Pharmaceutical Regulatory Affairs Consultants for Hire

Jalpesh B.

Pharmaceutical Formulation Development consultant
Create Project
★★★★★
☆☆☆☆☆
USD 20/hr
Master in pharmaceutics
India

OSD products like IR, DR, ER tablets, capsule, pellets/minitablets in capsules (Robust Formulation development, Troubleshooting, scale up troub...

★★★★★
☆☆☆☆☆
USD 20/hr
Contact3

Reema D.

14 years of experience in CMC author, Post-Approval Changes, Query Responses, XEVMPD
Create Project
★★★★★
☆☆☆☆☆
USD 50/hr
MBA
India

• Preparation of CTD sections of the dossiers required for Regulatory submission in various countries namely EU (National, MRP and DCP), US (AN...

★★★★★
☆☆☆☆☆
USD 50/hr
Contact3

Viky Gilles Daniel V.

Global Regulatory Affairs Consultant - FDA - Medical Device - Pharma
Create Project
★★★★★
☆☆☆☆☆
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 ...

★★★★★
☆☆☆☆☆
USD 150/hr
Contact3

Jessica B.

Global Project Leader in CNS | 10+ years of experience in clinical research | ACRP Certified
Create Project
★★★★★
☆☆☆☆☆
USD 50/hr
Master of Science in Clinical Mental Health Counseling
United States

Global Project Leader in Psychiatry & Neurology. Former Research Scientist in Psychiatry. Experienced ACRP Certified Clinical Research Coor...

★★★★★
☆☆☆☆☆
USD 50/hr
Contact3

Janita ..

Freelance content Medical Writer | Expertise in Clinical Research | Pharmacovigilance | Drug Regulatory affairs
Create Project
★★★★★
☆☆☆☆☆
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...

★★★★★
☆☆☆☆☆
USD 20/hr
Contact3

Venupriya D.

Intellectual Property Management- (IPM) IP reports for US, Europe, ROW markets, Daily update of OB & regulatory appr...
Create Project
★★★★★
☆☆☆☆☆
USD 50/hr
Masters of Science
India

Key Skills: • Graduate educational background in pharmaceuticals • Strong work experience in the pharmaceutical environment • Knowledge of inte...

★★★★★
☆☆☆☆☆
USD 50/hr
Contact3

Dr Gopirajan J.

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

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

★★★★★
☆☆☆☆☆
USD 15/hr
Contact3

Kolabtree is the leading online freelance marketplace for pharmaceutical regulatory affairs consulting experts. Post your project, get bids, and hire qualified experts quickly and easily.

pay-per-click
Confidentiality Assured

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.

Recent Projects
  • Hiring for pharmaceutical regulatory affairs consulting services
    $500.00
How it works View full page
1

Post your Project (Free)

Your project details are safe, secure and visible only to logged-in users.

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.