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Malignant Neoplasm of Breast

Oncology
13
Pipeline Programs
12
Companies
8
Clinical Trials
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
5
0
8
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Monoclonal Antibody
6100%
+ 11 programs with unclassified modality

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

11 companies ranked by most advanced pipeline stage

MSD
MSDIreland - Ballydine
4 programs
1
3
Imprime PGGPhase 21 trial
PembrolizumabPhase 2Monoclonal Antibody1 trial
Pembrolizumab Injection [Keytruda]Phase 21 trial
PembrolizumabPhase 1Monoclonal Antibody1 trial
Active Trials
NCT03435952Active Not Recruiting18Est. Oct 2026
NCT05159778Completed26Est. Apr 2023
NCT03289819Completed53Est. Jan 2021
+1 more trials
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
4 programs
1
3
Imprime PGGPhase 2
PembrolizumabPhase 2Monoclonal Antibody
Pembrolizumab Injection [Keytruda]Phase 2
PembrolizumabPhase 1Monoclonal Antibody
Bryan Corporation
Bryan CorporationOH - Cincinnati
1 program
1
Genomically Directed MonotherapyPhase 21 trial
Active Trials
NCT02101385Completed193Est. Sep 2022
HiberCell
HiberCellMA - Boston
1 program
1
Imprime PGGPhase 2
AstraZeneca
AstraZenecaCAMBRIDGE, United Kingdom
1 program
1
DS-8201aPhase 1
Biomed
BiomedAustralia - Sydney
1 program
1
PembrolizumabPhase 1Monoclonal Antibody
BioMed Valley Discoveries
1 program
1
PembrolizumabPhase 1Monoclonal Antibody
Pfizer
PfizerNEW YORK, NY
1 program
Ibrance Real World InsightsN/A1 trial
Active Trials
NCT03159195Completed652Est. Jun 2021
Daiichi Sankyo
Daiichi SankyoChina - Shanghai
1 program
DS-8201aPHASE_11 trial
Active Trials
NCT03366428Completed51Est. Feb 2021
Vera Therapeutics
Vera TherapeuticsBRISBANE, CA
1 program
Genomically Directed MonotherapyPHASE_2
Pierre Fabre
Pierre FabreFrance - Aignan
1 program
vinfluninePHASE_31 trial
Active Trials
NCT01953003Completed112Est. Jul 2017

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
Pierre Fabrevinflunine
MSDPembrolizumab Injection [Keytruda]
MSDImprime PGG
MSDPembrolizumab
Bryan CorporationGenomically Directed Monotherapy
MSDPembrolizumab
Daiichi SankyoDS-8201a
PfizerIbrance Real World Insights

Clinical Trials (8)

Total enrollment: 1,116 patients across 8 trials

Phase III Study of Vinflunine Plus Capecitabine Versus Capecitabine Alone in Patients With Advanced Breast Cancer

Start: Sep 2013Est. completion: Jul 2017112 patients
Phase 3Completed
NCT05033756MSDPembrolizumab Injection [Keytruda]

Comprehensive Analysis of Predictors of the Treatment With Pembrolizumab and Olaparib in Patients With Unresectable or Metastatic HER2 Negative Breast Cancer and a Deleterious Germline Mutation or a Homologous Recombination Deficiency (COMPRENDO

Start: Jul 2022Est. completion: Feb 202611 patients
Phase 2Active Not Recruiting
NCT05159778MSDImprime PGG

Phase 2 Study of Imprime PGG and Pembrolizumab in Patients With HR+/HER2- Metastatic Breast Cancer (mBCA)

Start: Nov 2021Est. completion: Apr 202326 patients
Phase 2Completed
NCT03289819MSDPembrolizumab

Neoadjuvant Pembrolizumab(Pbr)/Nab-Paclitaxel Followed by Pbr/Epirubicin/Cyclophosphamide in TNBC

Start: Mar 2018Est. completion: Jan 202153 patients
Phase 2Completed
NCT02101385Bryan CorporationGenomically Directed Monotherapy

Randomized Controlled Trial of Genomically Directed Therapy in Patients With Triple Negative Breast Cancer

Start: Apr 2014Est. completion: Sep 2022193 patients
Phase 2Completed
NCT03435952MSDPembrolizumab

Pembrolizumab With Intratumoral Injection of Clostridium Novyi-NT

Start: Jul 2018Est. completion: Oct 202618 patients
Phase 1Active Not Recruiting

Phase 1 Study to Evaluate the Effect of DS-8201a on the QT/QTc Interval and Pharmacokinetics in HER2-Expressing Breast Cancer

Start: Dec 2017Est. completion: Feb 202151 patients
Phase 1Completed
NCT03159195PfizerIbrance Real World Insights

Ibrance Real World Insights

Start: Jun 2017Est. completion: Jun 2021652 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

12 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.