Parexel
Focus: Parexel is a large Contract Research Organization (CRO) headquartered in Boston with 10,001–50,000 employees, providing clinical development, regulatory, and operations services across the pharmaceutical development lifecycle. As a major CRO, it executes trials and regulatory strategies for global pharma and biotech clients.
Profile data last refreshed 18h ago · AI intelligence enriched 1w ago
Funding Stage
PRIVATE
Employees
10001-50000
Open Jobs
320+173 this month
Hot — 436 jobs added in 30d
Net +173 (436 new, 263 removed). Aggressive expansion phase.
Should You Work at Parexel?
AI assessmentParexel is an excellent destination for clinical operations, regulatory affairs, and project management professionals seeking large-scale trial portfolio exposure and geographic expansion opportunities, but private status and limited visa sponsorship warrant due diligence on stability and relocation policies.
Why Work Here
- Massive pipeline exposure: 30 active programs spanning Phase 1–3 across oncology, respiratory, metabolic, and rare disease — ideal for clinical development and regulatory professionals seeking diverse therapeutic area experience.
Data completeness
4/9 — Basic
Company HealthSolid
Pipeline
Early-stage
50 total
LOE Risk
Protected
No near-term cliffs
Hiring
Stable
Automated analysis based on publicly available data (FDA, SEC, ClinicalTrials.gov). May be incomplete or delayed. This score does not reflect insider knowledge and should not be used as the sole basis for investment or employment decisions.
Pipeline & Clinical Trials
Blood draw
AsthmaMetvix
Actinic KeratosisClinical Trials (1)
Help build intelligence for Parexel
No one has shared interview or compensation data for this company yet. You'll earn 7 days of Pro access.
Data Sources
- Drug label: DailyMed / FDA
- Clinical trials: ClinicalTrials.gov
- Patent data: FDA Orange Book
- Spending data: CMS Medicare
The information on this page is for informational purposes only and should not be used as a substitute for professional medical advice. Drug information is sourced from FDA, DailyMed, and other government databases. Adverse event data from FAERS does not establish causation. Always consult a healthcare professional for medical decisions.