01Remote
IND strategy and authoring
Gap analysis through submission for a first-in-human program
6-12 weeksFind regulatory affairs consultant jobs across submissions, CMC, and lifecycle work.
Create a free profile around the regulatory work you can own, from IND strategy and FDA meeting preparation to Module 3 and post-approval support. Set your rate and availability, then let pharma and biotech companies contact you about relevant consulting work.
Free to create. You decide which opportunities to consider.
Regulatory Affairs profile focusIND and NDA strategy, FDA meetings, CMC documentation.
Your experience is valuable
Put your pharma and biotech experience in front of growing teams.
Consultants on FindPharmaPros have worked across organizations like these. Build your profile around the projects, systems, and milestones you know best.
Amgen
AstraZeneca
Biogen
Boehringer Ingelheim
Ginkgo Bioworks
Halia Therapeutics
Locus Biosciences
MedImmune
Merck
Novartis
Pfizer
Precision BioSciences
SELLAS Life SciencesProject fit
Regulatory projects that reward submission depth and product knowledge.
Use the closest examples to show the scope, responsibility, and working format you know.
02Remote
FDA meeting preparation
Briefing package, question strategy, and rehearsal for a Type B or C meeting
3-6 weeks03Remote
CMC documentation
Module 3 authoring and review across drug substance and product
2-6 months04Remote
Post-approval lifecycle
Supplements, labeling changes, and annual reports for marketed products
Fractional, ongoing05Remote
Regulatory due diligence
Data-room review of a licensing or acquisition target
1-3 weeksEvidence over labels
Specific regulatory evidence carries more weight than a broad title.
Concrete work helps companies understand what you can own faster than a broad list of responsibilities.
- Former FDA reviewers advising on meeting strategy
- CMC specialists in biologics and cell or gene therapy
- Combination-product and 510(k)/PMA experience
A useful consultant profile
Make three things clear before a conversation starts.
- 01
Name the work you can own
Use specific deliverables, systems, study stages, and project outcomes.
- 02
Set your working preferences
Add your availability, rate, and preferred working format.
- 03
Choose which conversations fit
Review each opportunity and decide whether it is worth exploring.
Public profile privacy: your public name appears as your first name and last initial.
Create your free profilePractical details
Regulatory Affairs consulting questions.
Getting found, choosing opportunities, setting your rate, and showing the experience companies need.
Create a free profile that shows your submission experience, therapeutic areas, product types, availability, and rate. Companies can then understand your fit and contact you directly about relevant regulatory work.
Yes, where your employment terms allow outside work. Your public profile uses your first name and last initial, and you decide what information to share during a conversation.
Set the rate that reflects your experience and the work you want to consider. Publishing it on your profile helps a company understand your expectations before starting a conversation.
Specific submission history makes a profile useful: INDs taken to clearance, NDA or BLA modules authored, FDA meetings led, and the therapeutic areas or product types behind that work.
Much of it can be. Submissions, briefing documents, and CMC writing are commonly remote, while in-person meeting support or team workshops depend on the engagement.
Ready for your next consulting project?
Create your free profile