PACIRA BIOSCIENCES INC

Insider Trading & Executive Data

PCRX
NASDAQ
Healthcare
Drug Manufacturers - Specialty & Generic

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52 insider trades in the last year. Go beyond summary counts with transaction-level detail, compensation intelligence, and institutional ownership context.

Trade-level insider transactions with filing links, transaction codes, and footnotes
Executive compensation trends by role with year-over-year comparisons
Institutional ownership shifts by quarter with top-holder concentration data
Form 144 and Form 8-K monitoring with AI analysis and CSV export tools

Insider Activity Summary

Insider Trades (1Y)
52
8 in last 30 days
Buy / Sell (1Y)
26/26
Acquisitions / Dispositions
Unique Insiders (1Y)
15
Active in past year
Insider Positions
20
Current holdings
Position Status
20/0
Active / Exited
Institutional Holders
237
Latest quarter
Board Members
69

Compensation & Governance

Avg Total Compensation
$3.2M
Latest year: 2024
Executives Covered
12
Comp records available
Form 8-K Events (1Y)
2
Personnel Changes (1Y)
1
Bonus Plan Events (1Y)
0
Organization Changes (1Y)
1
Board Appointments (1Y)
1
Board Departures (1Y)
0

Restricted Sales

Form 144 Filings (1Y)
12
Form 144 Insiders (1Y)
7
Planned Sale Shares (1Y)
87.3K
Planned Sale Value (1Y)
$2.1M
Price
$22.07
Market Cap
$900.5M
Volume
5,923
EPS
$0.16
Revenue
$726.4M
Employees
790
About PACIRA BIOSCIENCES INC

Company Overview

Pacira BioSciences is a commercial-stage biopharmaceutical and medical device company focused on non‑opioid pain management, with flagship products EXPAREL (bupivacaine liposome injectable suspension), ZILRETTA (extended‑release intra‑articular triamcinolone) and the iovera cryoanalgesia device. EXPAREL is the dominant revenue driver (~78% of 2024 revenue; $549M), with manufacturing at a San Diego campus supplemented by third‑party contract manufacturers and a highly concentrated wholesaler channel (three wholesalers processed ~77% of 2024 revenue). Recent structural wins (permanent HCPCS J‑code for EXPAREL, NOPAIN Act reimbursement, a new C‑code for iovera), FDA manufacturing approval, an active pipeline including PCRX‑201 (RMAT designated), and a Feb‑2025 acquisition of GQ Bio shape near‑term commercial and R&D priorities. Key risks include generic/ANDA challenges, patent litigation, supplier continuity and contingent milestone liabilities that materially affect financial and operating outcomes.

Executive Compensation Practices

Given Pacira’s business mix, executive incentives are likely tied to commercial KPIs (EXPAREL vial volumes, kit/vial mix, pricing and gross margin) and pipeline/regulatory milestones (e.g., PCRX‑201 Phase 2 progress, pediatric or additional indications for marketed products). Cost and manufacturing metrics (scale‑up of San Diego capacity, CGMP/QSR compliance, inventory reserve management) and successful IP defense or favorable patent rulings are also natural performance levers because they materially affect cash flow and impairment risk (the company recorded a $163.2M goodwill impairment after adverse patent/generic outcomes). Like peers in the Drug Manufacturers – Specialty & Generic industry, total compensation will skew toward equity‑based long‑term incentives and milestone or stock‑price linked awards, complemented by cash bonuses tied to annual revenue, margin and M&A/integration targets (GQ Bio). Stock‑based compensation has been a material driver of reported tax and earnings volatility, so option/RSU design and vesting schedules will be important to align leadership around long‑term share appreciation and cash preservation given contingent liabilities and debt covenant considerations.

Insider Trading Considerations

Insider activity at Pacira will often cluster around clearly material events: clinical readouts (PCRX‑201), FDA/regulatory decisions, IP/patent rulings, reimbursement code changes, earnings releases and major M&A or financing announcements. Because EXPAREL dominates revenue and three wholesalers concentrate distribution, material commercial news (e.g., generic entry or sizeable contract wins) can rapidly shift valuation and trigger opportunistic insider buying or selling; the goodwill impairment after a generic ruling is a recent example of a material event that changed insider and market behavior. Expect routine use of Section 16 reporting, pre‑arranged 10b5‑1 plans and pre‑clearance/blackout windows around quarter ends and clinical milestones; insiders should also be mindful of healthcare/regulatory confidentiality (clinical data, FDA communications, CMS reimbursement timing) that creates strict trading restrictions. Finally, liquidity and financing dynamics (contingent milestones up to ~$372M, convertible notes/covenants, active buyback program) can influence timing of insider transactions—watch for insider sales prior to financing or increased insider purchases following IP wins or successful integration milestones.

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