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Locally Advanced or Metastatic Breast Cancer

Oncology
3
Pipeline Programs
6
Companies
6
Clinical Trials
1 recruiting
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
1
0
1
0
1
0
Early DiscoveryClinical DevelopmentMarket

Oncology is a $53.9B market in consolidation, dominated by a handful of megacap players with blockbuster franchises approaching patent expiration.

$53.9B marketConsolidating→ Stable30 products15 companies

Key Trends

  • Heavy patent cliff exposure (REVLIMID $3.9B LOE 2028, JAKAFI $1.9B LOE 2028)
  • Kinase inhibitors and immunomodulatory agents dominate spend; limited diversification in top 10
  • Clinical trial volume remains exceptionally high (29,145 trials) but concentration in Phase 1-2 signals early-stage pipeline challenges

Career Verdict

Strong near-term opportunity for R&D and medical affairs roles, but competitive landscape and patent cliff urgency favor specialists over generalists.

AI-generated market analysis based on FDA, CMS, ClinicalTrials.gov, and hiring data

Market Leaders

#1ELIQUISStable
$18.3B
Bristol Myers Squibb·Launch15.0yr
#2FARXIGAStable
$4.3B
AstraZeneca·Peak15.4yr
#3REVLIMIDDeclining
$3.9B
Bristol Myers Squibb·LOE Approaching1.8yr
#4XTANDIStable
$2.6B
Astellas·Peak10.7yr
#5IMBRUVICAStable
$2.4B
AbbVie·Peak8.9yr

Drug Class Breakdown

FXa Inhibitors
$18.3B(34%)

concentrated in single product

SGLT2 Inhibitors
$4.3B(8%)

single dominant product

Kinase Inhibitors
$4.0B(7%)

multi-product class, competitive

Immunomodulatory Agents (Cereblon)
$3.9B(7%)

facing near-term patent cliff

Androgen Receptor Antagonists
$2.6B(5%)

prostate cancer specialty

Protein Kinase Inhibitors
$2.4B(4%)

niche hematologic oncology

JAK Inhibitors
$1.9B(4%)

near-term LOE exposure

Career Outlook

Stable

Oncology remains a premium therapeutic area but faces structural headwinds: top 10 products account for >80% of spend, patent cliffs loom (REVLIMID 2028), and late-stage pipeline thinness suggests slower near-term growth. However, high trial volume and consolidation create demand for specialized expertise in regulatory, clinical operations, and lifecycle management. Pharma professionals with kinase inhibitor, immunomodulatory, or ADC experience are in highest demand.

Breaking In

Entry-level candidates should target CROs (Thermo Fisher, IQVIA), emerging biotech (BeiGene, BeOne), or contract manufacturing; oncology specialization requires demonstrated domain knowledge.

For Experienced Professionals

Experienced professionals should focus on lifecycle/patent strategy roles (high salary, low headcount) or pivot to emerging modalities (ADCs, bispecifics) to avoid commoditization in crowded kinase inhibitor space.

In-Demand Skills

Regulatory strategy & PDUFA navigationKinase inhibitor development (small molecule)Clinical trial operations & site managementLifecycle management & patent strategyMedical affairs (oncology-specific science)Manufacturing scale-up (small molecule & biotech)

Best For

Regulatory Affairs ManagerClinical Operations ManagerMedical Science Liaison (MSL) — OncologyLifecycle ManagerR&D Scientist (medicinal chemistry, ADME)Manufacturing Engineer

Hiring Landscape

$102K–$266K

Oncology hiring is actively concentrated at Thermo Fisher Scientific (CRO/CDMO services, 559 jobs), AstraZeneca (208 jobs), and emerging biotech players like BeiGene (185 jobs). Commercial roles dominate (412 jobs, $136K avg) but R&D positions offer the highest salary premium ($199K avg, 347 roles). Patent cliff urgency is creating acute demand for regulatory, CMC, and lifecycle management expertise.

1,946
Open Roles
5
Companies Hiring
5
Departments

Top Hiring Companies

208Stable
185Growing
167Growing
147Growing

By Department

Commercial(21%)
$136K
Research & Development(18%)
$199K
Clinical Operations(5%)
$181K
Medical Affairs(4%)
$266K
Manufacturing(5%)
$102K

Strong near-term hiring momentum, especially in CRO/CDMO and emerging biotech; Medical Affairs offers highest compensation but limited headcount.

Competitive Landscape

6 companies ranked by most advanced pipeline stage

Genor Biopharma
Genor BiopharmaChina - Shanghai
1 program
1
GB491+ FulvestrantPhase 31 trial
Active Trials
NCT05054751Completed275Est. Mar 2024
Sermonix Pharmaceuticals
1 program
1
LasofoxifenePhase 21 trial
Active Trials
NCT03781063Completed100Est. May 2025
ViiV Healthcare
ViiV HealthcareNC - Durham
1 program
1
Ixabepilone, 32 mg/m^2 + Lapatinib, 1000 mgPhase 1
Eisai
EisaiChina - Liaoning
2 programs
EribulinN/A1 trial
Eribulin mesylateN/A1 trial
Active Trials
NCT03027245Completed353Est. May 2022
NCT03437083Completed340Est. Jun 2018
GSK
GSKLONDON, United Kingdom
1 program
Ixabepilone, 32 mg/m^2 + Lapatinib, 1000 mgPHASE_11 trial
Active Trials
NCT00634088Terminated13Est. Jun 2010
MediLink Therapeutics
MediLink TherapeuticsChina - Suzhou
1 program
YL202 should be intravenously infusedPHASE_21 trial
Active Trials
NCT06439771Recruiting180Est. Jul 2028

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
Genor BiopharmaGB491+ Fulvestrant
MediLink TherapeuticsYL202 should be intravenously infused
Sermonix PharmaceuticalsLasofoxifene
GSKIxabepilone, 32 mg/m^2 + Lapatinib, 1000 mg
EisaiEribulin mesylate
EisaiEribulin

Clinical Trials (6)

Total enrollment: 1,261 patients across 6 trials

NCT05054751Genor BiopharmaGB491+ Fulvestrant

GB491 Combined With Fulvestrant for HR+ HER2- Locally Advanced or Metastatic Breast Cancer

Start: Sep 2021Est. completion: Mar 2024275 patients
Phase 3Completed
NCT06439771MediLink TherapeuticsYL202 should be intravenously infused

A Phase 2 Study to Evaluate the Efficacy, Safety and Pharmacokinetics of YL202 in Patients With BC

Start: Apr 2024Est. completion: Jul 2028180 patients
Phase 2Recruiting

Evaluation of Lasofoxifene Versus Fulvestrant in Advanced or Metastatic ER+/HER2- Breast Cancer With an ESR1 Mutation

Start: Sep 2019Est. completion: May 2025100 patients
Phase 2Completed
NCT00634088GSKIxabepilone, 32 mg/m^2 + Lapatinib, 1000 mg

Phase I Study of Ixabepilone Plus Lapatinib With or Without Capecitabine in the Treatment of Human Epidermal Growth Factor Receptor 2 (HER2)-Positive Breast Cancer

Start: Jun 2008Est. completion: Jun 201013 patients
Phase 1Terminated
NCT03437083EisaiEribulin mesylate

A Study to Investigate the Efficacy and Safety of Eribulin in Korean Breast Cancer Participants

Start: Jan 2018Est. completion: Jun 2018340 patients
N/ACompleted

Incidence and Resolution of Eribulin-Induced Peripheral Neuropathy

Start: Oct 2016Est. completion: May 2022353 patients
N/ACompleted

Related Jobs in Oncology

Phase Legend

PreclinicalLab & animal studies
Phase 1Safety & dosing
Phase 2Efficacy testing
Phase 3Large-scale trials
On MarketApproved & available

Key Insights

1 late-stage (Phase 3) programs, potential near-term approvals
1 actively recruiting trials targeting 1,261 patients
6 companies competing in this space

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.