01Build your consultant profile
Add your specialties, relevant experience, preferred working format, availability, and rate. Creating a profile is free.
Fractional pharma and biotech consulting jobs
Find consulting work that fits your life sciences experience.
Create a free profile for part-time, project, and fractional consulting work in regulatory affairs, clinical research, medical writing, biostatistics, drug safety, quality, and more. Set your rate and availability, then let US pharma and biotech companies contact you directly.
- Free to create a profile
- Set your own rate
- Companies contact you directly
FindPharmaProsDr. Rachel B.
Regulatory Affairs Consultant
Available nowContact MeHire Consultant- Hourly Rate
- From USD 185/hour
- Experience
- 18 years
- Education
- PhD, Pharmaceutical Sciences
Specializations
IND StrategyBLA SubmissionsFDA MeetingsBiologicsCMC Regulatory
About
Regulatory strategist for US biotech sponsors moving biologics from preclinical through licensure. Hands-on with submission authoring, agency interactions, and cross-functional regulatory planning.
Work Experience
- Independent Regulatory Consultant2018 to present
- Director, Regulatory Affairs, mid-size biotech2011 to 2018
Education
- PhD, Pharmaceutical SciencesUS research university
Languages
English, Portuguese
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 a 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 SciencesExplore consulting work by specialty
See where your experience can take you.
Choose your specialty to explore fractional, contract, and remote consulting work that companies may need, plus the experience to highlight on your profile.
01
Regulatory Affairs
IND and NDA strategy, FDA meetings, CMC documentation.
- IND strategy and authoring
- FDA meeting preparation
02
Clinical Research Associate
Monitoring, TMF review, and vendor oversight for active trials.
- Rescue monitoring
- TMF review before an inspection
03
Remote Clinical Research
Central monitoring, TMF audits, and data work, fully remote.
- Central monitoring coverage
- Remote TMF audit
04
Medical Writer
CSRs, regulatory documents, manuscripts and med comms.
- Clinical study report
- Protocol and amendments
05
Biostatistician
SAPs, SAS and R programming, CDISC datasets, DSMB support.
- Statistical analysis plan
- TLF programming
06
Pharmacovigilance
Case processing, PSMF, aggregate reports, signal management.
- Case processing surge
- PSMF build or refresh
07
Pharma QA / GxP
GCP audits, mock inspections, QMS builds, CAPA remediation.
- GCP site and vendor audits
- Mock FDA inspection
This is how companies find you
Show more than a job title.
Build your profile around the projects, systems, submissions, studies, and deliverables you know. Pharma and biotech teams can understand your fit before they contact you.
AH
Dr. Alicia H.
Regulatory Affairs, CMC
18 years guiding IND and NDA submissions for small-molecule and biologic programs.
From USD 185/hour
View ProfileContact MeHire Consultant
MT
Marcus T.
Clinical Operations
Former CRO program lead. Rescues delayed Phase II-III trials and vendor oversight.
From USD 150/hour
View ProfileContact MeHire Consultant
PN
Dr. Priya N.
Pharmacovigilance
Builds and audits safety systems for emerging biotechs, PSMF to signal management.
From USD 165/hour
View ProfileContact MeHire Consultant
How it works for consultants
Create your profile once. Let the right companies find you.
Instead of applying to one job at a time, show companies the work you can own and the kind of consulting opportunities you want to consider.
01
02Get contacted about relevant work
Pharma and biotech teams review your experience and contact you directly when they see a potential fit.
03Choose the projects that fit
Discuss the scope, timeline, rate, and working format, then move forward when the opportunity works for you.
Built around your consulting career
More control over the work you take on.
Use one focused profile to be found for flexible life sciences work while staying in control of your availability, rate, and the opportunities you pursue.
A profile that keeps working
Companies can discover your experience even when you are not spending time searching and applying for individual roles.
Direct company conversations
Speak with the team that needs your expertise and understand the project before deciding whether it fits.
Your rate and availability
Publish the rate, working preferences, and availability that reflect how you want to consult.
Flexible ways to work
Be considered for defined projects, part-time support, remote work, or longer fractional engagements.
Freeto create and maintain your profile
15+life sciences specialty areas
Directconversations with companies
Create your free profile From first message to paid work
Keep the project details and payment in one place.
Agree the scope, timeline, rate, contract, and confidentiality terms directly with the company. FindPharmaPros supports messaging, timesheets, invoices, and payment once the work begins.
Questions consultants ask
What to know before creating your profile.
Straight answers about getting found, choosing opportunities, setting your rate, privacy, and payment.
Create a free consultant profile that shows the work you can own, your experience, availability, working preferences, and rate. Companies can then find you and contact you directly about relevant fractional, contract, or project work.
Companies may need support in regulatory affairs, clinical operations, clinical research, medical writing, biostatistics, drug safety, quality assurance, CMC, medical affairs, data management, market access, and related life sciences specialties.
Yes. Creating and maintaining your profile is free. The 9.5% platform fee applies only when paid work is invoiced through FindPharmaPros.
Yes, if your employment agreement and company policies allow outside work. You control your availability and decide which opportunities you want to discuss.
Yes. Many projects in regulatory affairs, medical writing, biostatistics, drug safety, data management, and clinical operations can be completed remotely. Add your preferred working arrangement to your profile so companies know what fits.
Choose a rate that reflects your experience, specialty, level of responsibility, and the kind of work you want to take on. Publishing your rate helps companies approach you with better-matched opportunities.
Public profiles use your first name and last initial, with no photo or direct contact details. Companies can see the professional experience, specialties, availability, working preferences, and rate you choose to publish.
Ready for your next consulting project?
Create your profile and let pharma and biotech companies find you.
For pharma and biotech companies
Hire fractional pharma and biotech talent for the work your team needs now.
Browse experienced US consultants in regulatory affairs, clinical research, medical writing, biostatistics, drug safety, quality, and more. Compare relevant experience and rates, then contact consultants directly.
- Reviewed consultant profiles
- Experience and rates visible
- No employer markup
AH
Dr. Alicia H.
Regulatory Affairs, CMC
18 years guiding IND and NDA submissions for small-molecule and biologic programs.
From USD 185/hour
View ProfileContact MeHire Consultant
MT
Marcus T.
Clinical Operations
Former CRO program lead. Rescues delayed Phase II-III trials and vendor oversight.
From USD 150/hour
View ProfileContact MeHire Consultant
PN
Dr. Priya N.
Pharmacovigilance
Builds and audits safety systems for emerging biotechs, PSMF to signal management.
From USD 165/hour
View ProfileContact MeHire Consultant
Fractional talent for life sciences teams
See the kind of experience your project can call on.
Illustrative profiles show how specialties and company experience appear in the network. Browse the live directory to see current consultants.
Thomas E.
Biostatistics Consultant
Experience includes
Dr. Maya R.
Regulatory Affairs Consultant
Experience includes
Kenji N.
Process Validation Consultant
Experience includes
Daniel K.
Clinical Operations Lead
Experience includes
Lucia M.
Pharmacovigilance Specialist
Experience includes
Susan W.
Clinical Development Advisor
Experience includes
Naomi B.
Pharma Quality Consultant
Experience includes
Amina C.
Bioinformatics Consultant
Experience includes
Priya S.
Senior Medical Writer
Experience includes
Omar H.
CMC Development Consultant
Experience includes
Fractional expertise by function
Bring in the specialist your next milestone needs.
Search by function or deliverable, from a defined project to interim coverage and ongoing fractional support.
01
Regulatory Affairs
IND and NDA strategy, FDA meetings, CMC documentation.
- IND strategy and authoring
- FDA meeting preparation
02
Clinical Research Associate
Monitoring, TMF review, and vendor oversight for active trials.
- Rescue monitoring
- TMF review before an inspection
03
Remote Clinical Research
Central monitoring, TMF audits, and data work, fully remote.
- Central monitoring coverage
- Remote TMF audit
04
Medical Writer
CSRs, regulatory documents, manuscripts and med comms.
- Clinical study report
- Protocol and amendments
05
Biostatistician
SAPs, SAS and R programming, CDISC datasets, DSMB support.
- Statistical analysis plan
- TLF programming
06
Pharmacovigilance
Case processing, PSMF, aggregate reports, signal management.
- Case processing surge
- PSMF build or refresh
07
Pharma QA / GxP
GCP audits, mock inspections, QMS builds, CAPA remediation.
- GCP site and vendor audits
- Mock FDA inspection
Where fractional talent fits
Add experienced capacity without turning every need into a full-time hire.
Use fractional talent when the work is important, specialized, and easier to define than a permanent role.
01
Defined project work
Bring in a specialist for a submission, audit, study deliverable, safety report, data package, or other clear scope.
02
Interim coverage
Keep critical work moving during a leave, leadership gap, hiring cycle, reorganization, or sudden increase in workload.
03
Ongoing fractional support
Add senior expertise for a set number of hours or days when the need is recurring but not yet a full-time position.
FindPharmaProsDr. Rachel B.
Regulatory Affairs Consultant
Available nowContact MeHire Consultant- Hourly Rate
- From USD 185/hour
- Experience
- 18 years
- Education
- PhD, Pharmaceutical Sciences
Specializations
IND StrategyBLA SubmissionsFDA MeetingsBiologicsCMC Regulatory
About
Regulatory strategist for US biotech sponsors moving biologics from preclinical through licensure. Hands-on with submission authoring, agency interactions, and cross-functional regulatory planning.
Work Experience
- Independent Regulatory Consultant2018 to present
- Director, Regulatory Affairs, mid-size biotech2011 to 2018
Education
- PhD, Pharmaceutical SciencesUS research university
Languages
English, Portuguese
See the evidence before you reach out
Shortlist consultants by the work they have actually done.
A useful profile connects a title to real submissions, studies, systems, therapeutic areas, and deliverables. Your team can compare the evidence, availability, and rate before starting a conversation.
- Functional and therapeutic-area experience
- Specific submissions, studies, systems, and deliverables
- Availability and working preferences
- Published hourly rate
How hiring works
Go from search to a clear scope without an agency layer.
The company and consultant stay in the same conversation from the first message through the agreed work.
01Browse the network
Search open profiles by function, therapeutic area, development stage, and the work you need completed.
02Start a direct conversation
Contact the consultant whose experience matches your scope. There is no recruiter or intake call between you.
03Execute agreements and start work
Confirm the deliverables, timeline, rate, and working format directly with the specialist who will do the work.
Why FindPharmaPros
A more direct way to add life sciences expertise.
FindPharmaPros makes the information needed for a useful first conversation visible, then lets your team speak with the consultant directly.
Browse before you commit
Review consultant profiles before creating an account or speaking with a sales team.
Compare relevant evidence
Look beyond job titles to the submissions, studies, systems, and deliverables behind the experience.
Speak directly
Discuss the work with the consultant who would deliver it, without a recruiter controlling access.
Use talent flexibly
Agree a defined project, interim assignment, or longer fractional scope around what the team needs.
A working relationship you control
Agree the scope and terms directly with the consultant.
Companies and consultants agree their MSA, SOW, NDA, deliverables, timeline, and working format together. FindPharmaPros supports discovery, messaging, timesheets, invoicing, and payment.
Questions from hiring teams
What companies usually want to know first.
Understand the marketplace model, browse the network, and decide who is worth a conversation.
Yes. You can review consultant profiles, experience, specialties, availability, and rates before deciding who to contact.
The network includes regulatory affairs, clinical operations, medical writing, biostatistics, pharmacovigilance, quality, CMC, medical affairs, data management, market access, and related specialties.
Fractional consulting gives a company access to experienced talent for a defined share of their time. It can cover a project, an interim need, or recurring support without creating a full-time role.
Search the directory, open the profiles that fit the work, and contact the consultant directly. You can then agree the scope, timeline, rate, MSA, SOW, and NDA together.
No. Employers pay the consultant rate shown without an added staffing markup. The published 9.5% platform fee is deducted from the consultant side of the invoice.
Yes. Many regulatory, writing, statistics, safety, quality, and clinical operations scopes can be handled remotely. Profiles can also show location and working preferences when on-site or hybrid support is needed.
The company and consultant agree the MSA, SOW, NDA, and project terms directly. This keeps ownership of the working relationship with the people doing the work.
Start with the work