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Breast Neoplasm

Oncology
22
Pipeline Programs
19
Companies
22
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
3
2
14
0
1
2
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
350%
Monoclonal Antibody
350%
+ 29 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

18 companies ranked by most advanced pipeline stage

MSD
MSDIreland - Ballydine
7 programs
1
4
1
Pegylated Liposomal DoxorubicinPhase 41 trial
Pegylated Liposomal DoxorubicinPhase 21 trial
Pegylated Lyposomal DoxorubicinPhase 21 trial
doxorubicin, cyclophosphamide, paclitaxel, trastuzumabPhase 2Monoclonal Antibody1 trial
temozolomidePhase 21 trial
+2 more programs
Active Trials
NCT00736333Completed167Est. Jun 2010
NCT00687440Completed27Est. Oct 2008
NCT00779129Completed70Est. Aug 2007
+3 more trials
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
7 programs
1
4
1
Pegylated Liposomal DoxorubicinPhase 4
Pegylated Liposomal DoxorubicinPhase 2
Pegylated Lyposomal DoxorubicinPhase 2
doxorubicin, cyclophosphamide, paclitaxel, trastuzumabPhase 2Monoclonal Antibody
temozolomidePhase 2
+2 more programs
Prevail Therapeutics
2 programs
1
1
AbemaciclibPhase 3Small Molecule1 trial
AbemaciclibPhase 2Small Molecule1 trial
Active Trials
NCT04305236Terminated1Est. Feb 2022
NCT05169567Active Not Recruiting368Est. Dec 2027
Pfizer
PfizerNEW YORK, NY
2 programs
1
VinorelbinePhase 2
Post Marketing Surveillance Study to Observe Safety and Efficacy of IBRANCE®N/A1 trial
Active Trials
NCT03445637Completed552Est. Jul 2025
UNION therapeutics
UNION therapeuticsDenmark - Hellerup
1 program
1
PIK3CA inhibitorPhase 21 trial
Active Trials
NCT05594095Recruiting620Est. Dec 2026
Sandoz
SandozAustria - Kundl
1 program
1
RAD001, Letrozole 2.5mgPhase 21 trial
Active Trials
NCT00107016Completed267Est. Apr 2007
Bayer
BayerLEVERKUSEN, Germany
1 program
1
SagopilonePhase 21 trial
Active Trials
NCT00313248Completed65Est. Nov 2008
Servier
ServierFrance - Suresnes
1 program
1
trifluridine/tipiracilPhase 21 trial
Active Trials
NCT04489173Active Not Recruiting52Est. Nov 2025
AstraZeneca
AstraZenecaCAMBRIDGE, United Kingdom
2 programs
1
Drug-AZD8931Phase 11 trial
Implanted Medical DeviceN/A1 trial
Active Trials
NCT03202472Completed50Est. Feb 2019
NCT01596530Terminated3Est. May 2013
Medpace
MedpaceCINCINNATI, OH
1 program
1
131I-TenatumomabPhase 1Monoclonal Antibody1 trial
Active Trials
NCT02602067Terminated2Est. Apr 2017
United BioPharma
United BioPharmaTaiwan - Hsinchu
1 program
1
UB-921Phase 11 trial
Active Trials
NCT03013881Completed18Est. Apr 2019
Merck & Co.
Merck & Co.RAHWAY, NJ
3 programs
Pegylated Liposomal DoxorubicinN/A
Pegylated Liposomal DoxorubicinPHASE_2
Pegylated Lyposomal DoxorubicinPHASE_2
Genome & Company
Genome & CompanyKorea - Suwon
1 program
Microarray Analysis for Human Genetic DiseaseN/A
Human BioSciences
Human BioSciencesWV - Martinsburg
1 program
Microarray Analysis for Human Genetic DiseaseN/A1 trial
Active Trials
NCT00001898Completed1,500Est. May 2008
Pierre Fabre
Pierre FabreFrance - Aignan
1 program
NeratinibN/ASmall Molecule1 trial
Active Trials
NCT04388384Completed304Est. Sep 2024
Providence Therapeutics
1 program
CyclophosphamidePHASE_11 trial
Active Trials
NCT02950259Completed16Est. Sep 2025
Takeda
TakedaTOKYO, Japan
1 program
TAK-165PHASE_11 trial
Active Trials
NCT00034281Completed16Est. Sep 2003
Eisai
EisaiChina - Liaoning
1 program
Eribulin MesylatePHASE_1_21 trial
Active Trials
NCT02513472Completed258Est. Apr 2021

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
MSDPegylated Liposomal Doxorubicin
Prevail TherapeuticsAbemaciclib
UNION therapeuticsPIK3CA inhibitor
Serviertrifluridine/tipiracil
Prevail TherapeuticsAbemaciclib
MSDtemozolomide
MSDdoxorubicin, cyclophosphamide, paclitaxel, trastuzumab
BayerSagopilone
MSDPegylated Liposomal Doxorubicin
SandozRAD001, Letrozole 2.5mg
MSDPegylated Lyposomal Doxorubicin
EisaiEribulin Mesylate
United BioPharmaUB-921
Providence TherapeuticsCyclophosphamide
Medpace131I-Tenatumomab

Showing 15 of 22 trials with date data

Clinical Trials (22)

Total enrollment: 4,544 patients across 22 trials

NCT00779285MSDPegylated Liposomal Doxorubicin

Safety Study of CAELYX in Patients With Metastatic Breast Cancer Previously Treated With Anthracyclines (Study P04057)(TERMINATED)

Start: Feb 2006Est. completion: Aug 20061 patients
Phase 4Terminated

Abemaciclib (LY2835219) Plus Fulvestrant Compared to Placebo Plus Fulvestrant in Previously Treated Breast Cancer

Start: Mar 2022Est. completion: Dec 2027368 patients
Phase 3Active Not Recruiting

SNF Platform Study of HR+/ HER2-advanced Breast Cancer

Start: Dec 2022Est. completion: Dec 2026620 patients
Phase 2Recruiting
NCT04489173Serviertrifluridine/tipiracil

TAS102 in Patients With ER-positive, HER2-negative Advanced Breast Cancer

Start: Sep 2020Est. completion: Nov 202552 patients
Phase 2Active Not Recruiting

Neo-Adjuvant Abemaciclib With Fulvestrant in Patients With ER/PR +HER Negative Breast Cancer

Start: Jul 2020Est. completion: Feb 20221 patients
Phase 2Terminated
NCT00638963MSDtemozolomide

Temozolomide as a Prophylaxis Against Brain Recurrence in Participants With Metastatic Breast Cancer (P05225 AM2)

Start: Oct 2008Est. completion: Jun 20106 patients
Phase 2Terminated
NCT00550771MSDdoxorubicin, cyclophosphamide, paclitaxel, trastuzumab

Phase II Trial to Compare the Safety of Two Chemotherapy Plus Trastuzumab Regimens as Adjuvant Therapy for HER2-positive Breast Cancer (Study P05048)

Start: Jul 2007Est. completion: Aug 2010181 patients
Phase 2Completed

Evaluation of a New Agent for Treatment of Advanced Stage Breast Cancer

Start: Apr 2006Est. completion: Nov 200865 patients
Phase 2Completed
NCT00687440MSDPegylated Liposomal Doxorubicin

A Study to Determine the Activity of Caelyx With Trastuzumab and Docetaxel in the Treatment of Metastatic Breast Cancer (Study P03679)

Start: Jul 2005Est. completion: Oct 200827 patients
Phase 2Completed
NCT00107016SandozRAD001, Letrozole 2.5mg

Everolimus and Letrozole as Preoperative Therapy of Primary Breast Cancer in Post-menopausal Women

Start: Mar 2005Est. completion: Apr 2007267 patients
Phase 2Completed
NCT00779129MSDPegylated Lyposomal Doxorubicin

A Study to Evaluate Safety and Efficacy of Caelyx in Combination With Cyclophosphamide in the Treatment of Metastatic Breast Cancer (P02948)

Start: Mar 2003Est. completion: Aug 200770 patients
Phase 2Completed
NCT02513472EisaiEribulin Mesylate

Study to Evaluate the Efficacy and Safety of Eribulin Mesylate in Combination With Pembrolizumab in Participants With Metastatic Triple-Negative Breast Cancer (mTNBC)

Start: Aug 2015Est. completion: Apr 2021258 patients
Phase 1/2Completed

A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of UB-921 in Healthy Volunteers

Start: Mar 2018Est. completion: Apr 201918 patients
Phase 1Completed

Pre-operative IRX-2 in Early Stage Breast Cancer (ESBC)

Start: Feb 2017Est. completion: Sep 202516 patients
Phase 1Completed
NCT02602067Medpace131I-Tenatumomab

131Iodine-Tenatumomab Treatment in Tenascin-C Positive Cancer Patients

Start: Nov 2015Est. completion: Apr 20172 patients
Phase 1Terminated

Evaluation of Drug Activity in Women With Breast Cancer and no Previous Herceptin Treatment

Start: Jun 2012Est. completion: May 20133 patients
Phase 1Terminated

Safety and Tolerability Study of TAK-165 in Subjects With Tumors Expressing HER2

Start: Jun 2002Est. completion: Sep 200316 patients
Phase 1Completed

Real-life Pan-HER-blockade With Neratinib

Start: Jul 2020Est. completion: Sep 2024304 patients
N/ACompleted
NCT03445637PfizerPost Marketing Surveillance Study to Observe Safety and Efficacy of IBRANCE®

Post Marketing Surveillance Study to Observe Safety and Efficacy of IBRANCE®

Start: Feb 2018Est. completion: Jul 2025552 patients
N/ACompleted
NCT03202472AstraZenecaImplanted Medical Device

Radiofrequency Identification Technology in Locating Non-palpable Breast Lesions in Patients Undergoing Surgery

Start: Aug 2017Est. completion: Feb 201950 patients
N/ACompleted
NCT00736333MSDPegylated Liposomal Doxorubicin

A Study to Evaluate Safety and Tolerability in Patients With Metastatic Breast Cancer Receiving Treatment With Caelyx (Study P04878)(COMPLETED)

Start: Nov 2006Est. completion: Jun 2010167 patients
N/ACompleted
NCT00001898Human BioSciencesMicroarray Analysis for Human Genetic Disease

Microarray Analysis for Human Genetic Disease

Start: Jun 1999Est. completion: May 20081,500 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 4,544 patients
19 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.