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Advanced or Metastatic Breast Cancer

Oncology
8
Pipeline Programs
10
Companies
9
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
1
2
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
267%
ADC
133%
+ 7 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

10 companies ranked by most advanced pipeline stage

Miracogen
MiracogenChina - Shanghai
1 program
1
MRG002Phase 21 trial
Active Trials
NCT04742153Unknown66Est. Feb 2023
Pfizer
PfizerNEW YORK, NY
1 program
1
PF-07220060 CDK4 inhibitorPhase 21 trial
Active Trials
NCT06105632Active Not Recruiting333Est. Jan 2028
AstraZeneca
AstraZenecaCAMBRIDGE, United Kingdom
1 program
1
AZD5363 when combined with weekly paclitaxel.Phase 1/21 trial
Active Trials
NCT01625286Completed148Est. Oct 2022
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
1 program
1
DinaciclibPhase 1Small Molecule
MSD
MSDIreland - Ballydine
1 program
1
DinaciclibPhase 1Small Molecule1 trial
Active Trials
NCT01676753Completed32Est. Feb 2022
Sandoz
SandozAustria - Kundl
1 program
1
LEE011Phase 11 trial
Active Trials
NCT02154776Completed13Est. Oct 2016
Menarini
MenariniGermany - Dresden
1 program
1
MEN1611Phase 11 trial
Active Trials
NCT03767335Completed62Est. Feb 2024
Adlai Nortye
Adlai NortyeNORTH BRUNSWICK, NJ
1 program
1
pelareorepPhase 11 trial
Active Trials
NCT05519059Completed15Est. May 2023
Rain Oncology
Rain OncologyCA - Newark
1 program
MilademetanPHASE_21 trial
Active Trials
NCT05932667Terminated1Est. Nov 2023
Daiichi Sankyo
Daiichi SankyoChina - Shanghai
1 program
Trastuzumab deruxtecanPHASE_3ADC1 trial
Active Trials
NCT04494425Active Not Recruiting866Est. Jun 2026

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
Daiichi SankyoTrastuzumab deruxtecan
PfizerPF-07220060 CDK4 inhibitor
Rain OncologyMilademetan
MiracogenMRG002
AstraZenecaAZD5363 when combined with weekly paclitaxel.
Adlai Nortyepelareorep
MenariniMEN1611
MSDDinaciclib
SandozLEE011

Clinical Trials (9)

Total enrollment: 1,536 patients across 9 trials

NCT04494425Daiichi SankyoTrastuzumab deruxtecan

Study of Trastuzumab Deruxtecan (T-DXd) vs Investigator's Choice Chemotherapy in HER2-low, Hormone Receptor Positive, Metastatic Breast Cancer

Start: Jul 2020Est. completion: Jun 2026866 patients
Phase 3Active Not Recruiting
NCT06105632PfizerPF-07220060 CDK4 inhibitor

A Study to Learn About the Study Medicine Called PF-07220060 in Combination With Fulvestrant in People With HR-positive, HER2-negative Advanced or Metastatic Breast Cancer Who Progressed After a Prior Line of Treatment

Start: Jan 2024Est. completion: Jan 2028333 patients
Phase 2Active Not Recruiting

Milademetan and Fulvestrant in GATA3-mutant, ER+HER- Advanced or Metastatic Breast Cancer

Start: Oct 2023Est. completion: Nov 20231 patients
Phase 2Terminated

A Study of MRG002 in the Treatment of Patients With HER2-low Locally Advanced or Metastatic Breast Cancer (BC)

Start: May 2021Est. completion: Feb 202366 patients
Phase 2Unknown
NCT01625286AstraZenecaAZD5363 when combined with weekly paclitaxel.

Investigating Safety, Tolerability and Efficacy of AZD5363 When Combined With Paclitaxel in Breast Cancer Patients

Start: Oct 2012Est. completion: Oct 2022148 patients
Phase 1/2Completed

Pelareorep and Paclitaxel Injection in Chinese Patients With Advanced or Metastatic Breast Cancer

Start: Oct 2021Est. completion: May 202315 patients
Phase 1Completed

MEN1611 With Trastuzumab (+/- Fulvestrant) in Metastatic Breast Cancer

Start: Nov 2018Est. completion: Feb 202462 patients
Phase 1Completed
NCT01676753MSDDinaciclib

Phase 1b Trial of Dinaciclib With Pembrolizumab for Advanced Breast Cancer

Start: Dec 2016Est. completion: Feb 202232 patients
Phase 1Completed

Dose Escalation Study of LEE011 in Combination With Buparlisib and Letrozole in HR+, HER2-negative Post-menopausal Women With Advanced Breast Cancer.

Start: Jun 2014Est. completion: Oct 201613 patients
Phase 1Completed

Related Jobs in Oncology

Phase Legend

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

Key Insights

10 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.