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Neoplasm

Oncology
23
Pipeline Programs
18
Companies
25
Clinical Trials
2 recruiting
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
19
3
1
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
444%
Monoclonal Antibody
444%
ADC
111%
+ 23 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

Bayer
BayerLEVERKUSEN, Germany
1 program
1
NexavarPhase 21 trial
Active Trials
NCT00657254Completed9Est. Jun 2005
MSD
MSDIreland - Ballydine
4 programs
3
1
MK2461Phase 1/2
DalotuzumabPhase 1Monoclonal Antibody
RidaforolimusPhase 1
preladenantPhase 1
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
4 programs
3
1
MK2461Phase 1/21 trial
DalotuzumabPhase 1Monoclonal Antibody1 trial
RidaforolimusPhase 11 trial
preladenantPhase 11 trial
Active Trials
NCT00694356Completed15Est. Apr 2009
NCT00694083Completed13Est. Sep 2009
NCT03099161Terminated10Est. Feb 2018
+1 more trials
Biocorp
BiocorpFrance - Issoire
2 programs
1
1
Pegylated Recombinant Human Arginase IPhase 1/21 trial
Pegylated Recombinant Human Arginase IPhase 11 trial
Active Trials
NCT00988195Completed15Est. Aug 2009
NCT01092091Completed20Est. Feb 2012
Prevail Therapeutics
5 programs
5
AbemaciclibPhase 1Small Molecule1 trial
GalunisertibPhase 1Small Molecule1 trial
LY3023414Phase 11 trial
OlaratumabPhase 1Monoclonal Antibody1 trial
PrexasertibPhase 1Small Molecule1 trial
Active Trials
NCT02117648Completed26Est. Aug 2015
NCT02304419Completed10Est. Aug 2016
NCT02536586Completed12Est. Feb 2017
+2 more trials
Piramal Pharma
Piramal PharmaMumbai, India
2 programs
2
P276-00Phase 11 trial
P276-00Phase 11 trial
Active Trials
NCT00408018Terminated28Est. Oct 2008
NCT00407498Completed50Est. Sep 2008
Compugen
CompugenCA - San Francisco
1 program
1
COM503Phase 11 trial
Active Trials
NCT06759649Recruiting200Est. Nov 2027
Kite Pharma
Kite PharmaCA - El Segundo
1 program
1
COM503Phase 1
Pfizer
PfizerNEW YORK, NY
1 program
1
PF-00337210Phase 11 trial
Active Trials
NCT01105533Completed46Est. Sep 2011
Sandoz
SandozAustria - Kundl
1 program
1
TKI258Phase 11 trial
Active Trials
NCT01155713Completed63Est. Nov 2013
AstraZeneca
AstraZenecaCAMBRIDGE, United Kingdom
1 program
1
[14C] AZD6738Phase 11 trial
Active Trials
NCT06754761Not Yet Recruiting8Est. Aug 2025
Boehringer Ingelheim
Boehringer IngelheimINGELHEIM, Germany
2 programs
ARBN/A3 trials
BI 891065PHASE_11 trial
Active Trials
NCT07544654Not Yet Recruiting390Est. May 2030
NCT07472517Recruiting670Est. Jul 2029
NCT02215733Completed1,165,781
+1 more trials
Merck & Co.
Merck & Co.RAHWAY, NJ
2 programs
DalotuzumabPHASE_1Monoclonal Antibody
MK2461PHASE_1_2
SpringWorks Therapeutics
1 program
PF-03084014N/A
Colorado Therapeutics
Colorado TherapeuticsCO - Louisville
1 program
PF-03084014N/A1 trial
Active Trials
NCT02955446No Longer Available
Eli Lilly and Company
Eli Lilly and CompanyINDIANAPOLIS, IN
1 program
AbemaciclibPHASE_1Small Molecule
Gilead Sciences
Gilead SciencesFOSTER CITY, CA
1 program
COM503PHASE_1
Sanofi
SanofiPARIS, France
1 program
Tusamitamab ravtansinePHASE_1ADC2 trials
Active Trials
NCT05429762Terminated56Est. Apr 2024
NCT04659603Terminated50Est. Jan 2025

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
Boehringer IngelheimARB
Boehringer IngelheimARB
SanofiTusamitamab ravtansine
BayerNexavar
BiocorpPegylated Recombinant Human Arginase I
Sharp TherapeuticsMK2461
AstraZeneca[14C] AZD6738
CompugenCOM503
SanofiTusamitamab ravtansine
Boehringer IngelheimBI 891065
Sharp Therapeuticspreladenant
Prevail TherapeuticsPrexasertib
Prevail TherapeuticsLY3023414
Prevail TherapeuticsGalunisertib
Prevail TherapeuticsOlaratumab

Showing 15 of 24 trials with date data

Clinical Trials (25)

Total enrollment: 1,167,547 patients across 25 trials

DAREON-NEC-1: A Study in People With Advanced Extrapulmonary Neuroendocrine Cancer to Compare Obrixtamig Plus Carboplatin and Etoposide Treatment With Standard Chemotherapy

Start: Jun 2026Est. completion: May 2030390 patients
Phase 3Not Yet Recruiting

DAREON ® -Lung-1: A Study in People With Advanced Small Cell Lung Cancer to Compare Obrixtamig Plus Atezolizumab, Carboplatin, and Etoposide Treatment With Standard Chemotherapy

Start: Apr 2026Est. completion: Jul 2029670 patients
Phase 3Recruiting
NCT04659603SanofiTusamitamab ravtansine

Tusamitamab Ravtansine Monotherapy and in Combination in Patients With CEACAM5-positive Advanced Solid Tumors

Start: Mar 2021Est. completion: Jan 202550 patients
Phase 2Terminated

Extension Program for Bay 43-9006

Start: Dec 2002Est. completion: Jun 20059 patients
Phase 2Completed
NCT01092091BiocorpPegylated Recombinant Human Arginase I

Study of Pegylated Human Recombinant Arginase for Liver Cancer (BCT-100-002)

Start: Mar 2010Est. completion: Feb 201220 patients
Phase 1/2Completed

MK2461 Phase I/II Study in Patients With Advanced Solid Tumors (MK-2461-002 AM1)(COMPLETED)

Start: Jun 2007Est. completion: Nov 200826 patients
Phase 1/2Completed

Human ADME Study of [14C]-Ceralasertib (AZD6738) and Absolute Bioavailability of Ceralasertib

Start: Jan 2025Est. completion: Aug 20258 patients
Phase 1Not Yet Recruiting

A Clinical Trial to Assess COM503 in Participants With Advanced Solid Malignancies

Start: Jan 2025Est. completion: Nov 2027200 patients
Phase 1Recruiting
NCT05429762SanofiTusamitamab ravtansine

Effect of Tusamitamab Ravtansine on QTc Interval in Participants With Metastatic Solid Tumors

Start: Oct 2022Est. completion: Apr 202456 patients
Phase 1Terminated

A Study to Test Different Doses of BI 891065 Alone and in Combination With BI 754091 in Asian Patients With Different Types of Advanced Cancer (Solid Tumours)

Start: Nov 2019Est. completion: May 202312 patients
Phase 1Completed

Study of Preladenant (MK-3814) Alone and With Pembrolizumab (MK-3475) in Participants With Advanced Solid Tumors (MK-3814A-062)

Start: Jun 2017Est. completion: Feb 201810 patients
Phase 1Terminated

A Study of Prexasertib (LY2606368) in Japanese Participants With Advanced Cancers

Start: Oct 2015Est. completion: Apr 201712 patients
Phase 1Completed

A Study of LY3023414 in Japanese Participants With Advanced Cancer

Start: Sep 2015Est. completion: Feb 201712 patients
Phase 1Completed

A Study of Galunisertib on the Immune System in Participants With Cancer

Start: May 2015Est. completion: Aug 201610 patients
Phase 1Completed

A Study of Olaratumab in Japanese Participants With Advanced Cancer

Start: Mar 2015Est. completion: Jan 202025 patients
Phase 1Completed

A Study of LY2835219 in Participants With Cancer

Start: Apr 2014Est. completion: Aug 201526 patients
Phase 1Completed

Bioavailability and Food Effect Study of TKI258 (CSF Capsule vs. FMI Tablet) in Adult Patients With Advanced Solid Tumors

Start: Jul 2010Est. completion: Nov 201363 patients
Phase 1Completed

Study of Dalotuzumab (MK-0646) in Adults With Solid Tumors (MK-0646-009)

Start: Aug 2008Est. completion: Apr 200915 patients
Phase 1Completed

Study of Ridaforolimus (MK-8669) in Participants With Solid Tumors (MK-8669-003)(COMPLETED)

Start: Jun 2008Est. completion: Sep 200913 patients
Phase 1Completed
NCT00988195BiocorpPegylated Recombinant Human Arginase I

Study of Pegylated Human Recombinant Arginase for Liver Cancer

Start: May 2008Est. completion: Aug 200915 patients
Phase 1Completed

A Dose Finding Study Of A New Medication, PF-00337210 That Will Possibly Decrease Blood Supply To Tumors

Start: May 2006Est. completion: Sep 201146 patients
Phase 1Completed

Phase I Study of P276-00 in Patients With Advanced Refractory Neoplasms

Start: Mar 2006Est. completion: Oct 200828 patients
Phase 1Terminated

Open Label Phase I Study of P276-00 in Patients With Advanced Refractory Neoplasms

Start: May 2005Est. completion: Sep 200850 patients
Phase 1Completed

Compassionate Use Protocol for PF-03084014 in Patients With Advanced Solid Tumor Malignancies

N/ANo Longer Available

The Use of Angiotensin Receptor Blockers and the Risk of Cancer

Start: Feb 20111,165,781 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

2 actively recruiting trials targeting 1,167,547 patients
18 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.