Find fractional consulting work that fits your life sciences experience.
Create a free profile for part-time, project, and fractional work. Set your rate and availability, then let pharma and biotech companies contact you directly.
Free to create. You stay in control of every opportunity.

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.

Show more than a job title.
Build your profile around the projects, systems, submissions, studies, and deliverables you know. Companies can understand your fit before they contact you.
Create your free profile- 01
Where you specialize
Your function, therapeutic areas, and the development stages where you add the most value.
- 02
What you have delivered
The submissions, studies, systems, documents, and decisions that demonstrate your experience.
- 03
How you prefer to work
Your availability, location preferences, and the types of engagements that suit you.
- 04
What a conversation should cover
Your rate and enough practical detail for a company to approach you with a relevant scope.
Explore fractional consulting jobs by role.
Each guide explains the project types companies may need, what to include in your profile, and how to position your experience.
7 specialty guides
Regulatory Affairs
IND and NDA strategy, FDA meetings, CMC documentation.
IND strategy and authoring | FDA meeting preparation
02Clinical Research Associate
Monitoring, TMF review, and vendor oversight for active trials.
Rescue monitoring | TMF review before an inspection
03Remote Clinical Research
Central monitoring, TMF audits, and data work, fully remote.
Central monitoring coverage | Remote TMF audit
04Medical Writer
CSRs, regulatory documents, manuscripts and med comms.
Clinical study report | Protocol and amendments
05Biostatistician
SAPs, SAS and R programming, CDISC datasets, DSMB support.
Statistical analysis plan | TLF programming
06Pharmacovigilance
Case processing, PSMF, aggregate reports, signal management.
Case processing surge | PSMF build or refresh
07Pharma QA / GxP
GCP audits, mock inspections, QMS builds, CAPA remediation.
GCP site and vendor audits | Mock FDA inspection
More control over the work you take on.
Be known for specific work
A focused profile gives companies a faster way to understand your experience than a general resume.
Speak directly with companies
When your background fits a project, a company can contact you directly to discuss the work.
Choose what fits
You decide your availability, working preferences, and which opportunities are worth exploring.
Create your profile once. Let the right companies find you.
Four focused steps turn your experience into a profile that works for you.
- 01
Choose your areas of expertise
Start with the functions, therapeutic areas, and development stages where your experience is strongest.
- 02
Add evidence from your work
Describe the deliverables, systems, and outcomes that help a company understand your track record.
- 03
Set your availability and preferences
Tell companies when you are available, how you work, and the engagements you want to consider.
- 04
Publish after review
We review your profile for clarity, then make it discoverable to companies looking for your expertise.
Questions consultants often ask.
What to expect, how companies find you, and what makes a profile useful.
Create a free 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.
Experienced professionals in regulatory affairs, clinical operations, clinical research, medical writing, biostatistics, pharmacovigilance, quality, CMC, medical affairs, data management, market access, and related specialties can join.
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.
Yes. You choose your availability, working preferences, and rate. When a company contacts you, you decide whether the scope, timing, and working arrangement are right for you.
Specific evidence. Name the submissions, study phases, systems, document types, or inspection work you have handled. Add the therapeutic areas you know and describe the outcomes you helped achieve.
Create your profile and let pharma and biotech companies find you.
Set your rate and availability, then decide which opportunities are worth a conversation.
Create your free profile