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Tumors

Oncology
32
Pipeline Programs
26
Companies
50
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
24
7
1
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Small Molecule
1588%
Monoclonal Antibody
212%
+ 37 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

25 companies ranked by most advanced pipeline stage

AstraZeneca
AstraZenecaCAMBRIDGE, United Kingdom
2 programs
1
1
AZD2171Phase 21 trial
AZD1152 part APhase 11 trial
Active Trials
NCT00338182Completed43Est. Mar 2017
NCT00264004Completed119Est. Apr 2011
Sharp Therapeutics
Sharp TherapeuticsPA - Pittsburgh
7 programs
5
2
LenvatinibPhase 1/2Small Molecule
LenvatinibPhase 1/2Small Molecule
Biomarker sample collection before and after dosing with cytotoxic agentPhase 1
VorinostatPhase 1Small Molecule
ridaforolimusPhase 1
+2 more programs
MSD
MSDIreland - Ballydine
7 programs
5
2
LenvatinibPhase 1/2Small Molecule
LenvatinibPhase 1/2Small Molecule
Biomarker sample collection before and after dosing with cytotoxic agentPhase 11 trial
VorinostatPhase 1Small Molecule1 trial
ridaforolimusPhase 11 trial
+2 more programs
Active Trials
NCT00800865Completed36Est. Oct 2009
NCT00373490Completed16Est. Oct 2007
NCT00060645Completed33Est. Feb 2009
+2 more trials
Sandoz
SandozAustria - Kundl
5 programs
4
1
PTK787/ZK 222584Phase 1/21 trial
ASA404Phase 11 trial
EverolimusPhase 11 trial
LBH589Phase 11 trial
PatupilonePhase 11 trial
Active Trials
NCT01031212Withdrawn0Est. Jun 2013
NCT00187174Completed41Est. Oct 2008
NCT00412997Completed14
+2 more trials
Bayer
BayerLEVERKUSEN, Germany
2 programs
1
1
PTK787/ZK 222584Phase 1/2
SH U04722Phase 11 trial
Active Trials
NCT00375453Terminated10Est. Oct 2007
ViiV Healthcare
ViiV HealthcareNC - Durham
1 program
1
Oral TopotecanPhase 1/2
Pfizer
PfizerNEW YORK, NY
3 programs
3
AGS-22M6EPhase 1
SKI-606Phase 11 trial
TTI-237Phase 12 trials
Active Trials
NCT01001936Completed28Est. Dec 2008
NCT00195325Terminated45
NCT00195247Terminated45
Astellas
AstellasChina - Shenyang
1 program
1
AGS-22M6EPhase 11 trial
Active Trials
NCT01409135Completed34Est. Apr 2015
Prevail Therapeutics
1 program
1
CixutumumabPhase 1Monoclonal Antibody
Lixte Biotechnology
Lixte BiotechnologyBOCA RATON, FL
1 program
1
LB-100 for InjectionPhase 11 trial
Active Trials
NCT01837667Completed29Est. Sep 2016
Taiho Pharma
Taiho PharmaJapan - Tokyo
1 program
1
S-1Phase 1
Puma Biotechnology
Puma BiotechnologyLOS ANGELES, CA
1 program
1
neratinibPhase 1Small Molecule1 trial
Active Trials
NCT00397046Completed21Est. Mar 2009
Eisai
EisaiChina - Liaoning
5 programs
E7046PHASE_11 trial
E7090PHASE_11 trial
LenvatinibPHASE_1Small Molecule1 trial
LenvatinibPHASE_1_2Small Molecule1 trial
LenvatinibPHASE_1_2Small Molecule1 trial
Active Trials
NCT02540291Terminated31Est. Feb 2018
NCT02275910Completed40Est. Sep 2021
NCT02686164Completed51Est. Aug 2018
+2 more trials
Bristol Myers Squibb
3 programs
BMS-275183PHASE_11 trial
DasatinibPHASE_1Small Molecule1 trial
BMS-663513PHASE_1_21 trial
Active Trials
NCT00207025Terminated60
NCT00339144Completed16Est. Sep 2008
NCT00309023Terminated115Est. Sep 2009
Boehringer Ingelheim
Boehringer IngelheimINGELHEIM, Germany
2 programs
BIBF 1120PHASE_11 trial
BIBF 1120PHASE_11 trial
Active Trials
NCT02182206Completed50
NCT02182128Completed24
Biogen
BiogenCAMBRIDGE, MA
2 programs
CNF2024PHASE_11 trial
hCBE-11PHASE_11 trial
Active Trials
NCT00345189Completed70Est. Apr 2009
NCT00105170Terminated13Est. Aug 2006
Hutchmed
HutchmedChina - Hong Kong
2 programs
VolitinibPHASE_1Small Molecule1 trial
surufatinibPHASE_1_2Small Molecule1 trial
Active Trials
NCT01985555Completed85Est. Apr 2019
NCT02549937Completed130Est. Jun 2023
Merck & Co.
Merck & Co.RAHWAY, NJ
1 program
Biomarker sample collection before and after dosing with cytotoxic agentPHASE_1
Curis
CurisMA - Lexington
1 program
CUDC-101PHASE_11 trial
Active Trials
NCT00728793Completed25Est. Apr 2010
Parexel
ParexelMA - Boston
1 program
CixutumumabPHASE_1Monoclonal Antibody
Taiho Oncology
Taiho OncologyNJ - Princeton
1 program
S-1PHASE_11 trial
Active Trials
NCT00400023Completed12Est. May 2007
Zentalis Pharmaceuticals
1 program
ZN-c3PHASE_12 trials
Active Trials
NCT07546500Not Yet Recruiting420Est. Apr 2030
NCT05431582Withdrawn0Est. Dec 2022
GSK
GSKLONDON, United Kingdom
1 program
Oral TopotecanPHASE_1_21 trial
Active Trials
NCT00382733Completed26Est. Mar 2011
Novartis
NovartisBASEL, Switzerland
1 program
PTK787/ZK 222584PHASE_1_2
Sanofi
SanofiPARIS, France
1 program
RasburicasePHASE_45 trials
Active Trials
NCT04349306Completed50Est. Mar 2021
NCT01200485Completed55Est. Jul 2016
NCT01097369Terminated1Est. Feb 2010
+2 more trials

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
SanofiRasburicase
SanofiRasburicase
SanofiRasburicase
Zentalis PharmaceuticalsZN-c3
SanofiRasburicase
SanofiRasburicase
SanofiRasburicase
AstraZenecaAZD2171
SanofiRasburicase
SanofiRasburicase
SanofiRasburicase
Hutchmedsurufatinib
EisaiLenvatinib
EisaiLenvatinib
GSKOral Topotecan

Showing 15 of 50 trials with date data

Clinical Trials (50)

Total enrollment: 2,932 patients across 50 trials

Evaluate the Efficacy and Safety of Rasburicase (Fasturtec®) in the Prevention and Treatment of Hyperuricemia in Pediatric Patients With Non-Hodgkin's Lymphoma and Acute Leukemia

Start: May 2020Est. completion: Mar 202150 patients
Phase 4Completed

Study of Rasburicase as Treatment or Prevention of Hyperuricemia Associated With Tumor Lysis Syndrome in Patients With Relapsed or Refractory Lymphoma, Leukemia, or Solid Tumor Malignancy

Start: Mar 2004Est. completion: Jul 200694 patients
Phase 4Completed

Rasburicase for Treatment of Hyperuricemia in Children and Adolescence Patients With Tumor Lysis Syndrome

Start: Mar 2003Est. completion: Jan 200438 patients
Phase 4Completed

A Study of Azenosertib (ZN-c3) Versus Investigator's Choice Chemotherapy in Subjects With Platinum-Resistant High-Grade Serous Ovarian, Primary Peritoneal, or Fallopian Tube Cancers Positive for Cyclin E1 Protein Expression

Start: Apr 2026Est. completion: Apr 2030420 patients
Phase 3Not Yet Recruiting

Rasburicase (Fasturtec) Registration Trial

Start: Oct 2007Est. completion: Jan 200910 patients
Phase 3Terminated

Rasburicase Versus Allopurinol in Tumor Patients at Risk for Hyperuricemia and Tumor Lysis Syndrome

Start: Apr 2004Est. completion: Dec 2007280 patients
Phase 3Completed

Rasburicase in Patients at High Risk for Tumor Lysis Syndrome (TLS) During Cycle-2

Start: Apr 2011Est. completion: Jul 201655 patients
Phase 2Completed

Study to Investigate the Management of Hypertension and Efficacy of AZD2171 in Patients With Advanced Solid Tumours

Start: Nov 2005Est. completion: Apr 2011119 patients
Phase 2Completed

Rasburicase for Hyperuricemia

Start: Jun 2005Est. completion: Apr 200630 patients
Phase 2Completed

Rasburicase as a Uricolytic Therapy for Hyperuricemia in Patients With Leukemia or Lymphoma

Start: Apr 2003Est. completion: Jun 200450 patients
Phase 2Completed

Rasburicase for the Treatment/Prevention of Hyperuricemia in Adult Patients With Relapsing Aggressive Non Hodgkin's Lymphoma

Start: Jul 2002Est. completion: Jan 200533 patients
Phase 2Terminated

A Multi-Center, Open-Label Study of Surufatinib (HMPL-012) in Patients With Advanced Solid Tumors

Start: Nov 2015Est. completion: Jun 2023130 patients
Phase 1/2Completed

A Trial of Lenvatinib (E7080) Plus Pembrolizumab in Participants With Selected Solid Tumors

Start: Jul 2015Est. completion: Jul 2022357 patients
Phase 1/2Completed

Study of Lenvatinib in Children and Adolescents With Refractory or Relapsed Solid Malignancies and Young Adults With Osteosarcoma

Start: Dec 2014Est. completion: Jul 2022117 patients
Phase 1/2Completed
NCT00382733GSKOral Topotecan

Oral Topotecan to Treat Recurrent or Persistent Solid Tumors

Start: Nov 2006Est. completion: Mar 201126 patients
Phase 1/2Completed

Pharmacokinetic Evaluation of Rasburicase in Patients With Leukemia and/or Lymphoma at High Risk of TLS

Start: Jul 2006Est. completion: Apr 200718 patients
Phase 1/2Completed

Study of BMS-663513 in Patients With Advanced Cancer

Start: Dec 2005Est. completion: Sep 2009115 patients
Phase 1/2Terminated
NCT00171587SandozPTK787/ZK 222584

Study of the Safety, Tolerability, Pharmacokinetics, and Anti-tumor Effects of Vatalanib in Combination With Capecitabine in Patients With Advanced Cancer

Start: May 2002Est. completion: Mar 200722 patients
Phase 1/2Completed

Phase I Study of ZN-c3 and Bevacizumab ± Pembrolizumab in Metastatic CCNE1 Amplified and TP53 Mutant Solid Tumors

Start: Dec 2022Est. completion: Dec 20220
Phase 1Withdrawn

Phase 1 Study to Determine the Effect of Lenvatinib (E7080) on the Pharmacokinetics of Midazolam in Subjects With Advanced Solid Tumors

Start: Apr 2016Est. completion: Aug 201851 patients
Phase 1Completed

Study of E7046 in Subjects With Selected Advanced Malignancies

Start: Jul 2015Est. completion: Feb 201831 patients
Phase 1Terminated

Phase 1 Study of E7090 in Subjects With Solid Tumor

Start: Oct 2014Est. completion: Sep 202140 patients
Phase 1Completed

Phase I Study of the Volitinib (HMPL-504) in Patients With Advanced Solid Tumors

Start: May 2013Est. completion: Apr 201985 patients
Phase 1Completed
NCT01837667Lixte BiotechnologyLB-100 for Injection

Phase I Study of LB-100 With Docetaxel in Solid Tumors

Start: Feb 2013Est. completion: Sep 201629 patients
Phase 1Completed

A Study of the Safety and Pharmacokinetics of AGS-22M6E in Subjects With Malignant Solid Tumors That Express Nectin-4

Start: Jul 2011Est. completion: Apr 201534 patients
Phase 1Completed

ASA404 in Combination With Carboplatin/Paclitaxel/Cetuximab in Treating Patients With Refractory Solid Tumors

Start: Jan 2010Est. completion: Jun 20130
Phase 1Withdrawn
NCT00800865MSDBiomarker sample collection before and after dosing with cytotoxic agent

A Study to Evaluate Biomarkers in Patients With Solid Tumors (0000-097)(COMPLETED)

Start: Jan 2009Est. completion: Oct 200936 patients
Phase 1Completed

A Phase I Study of the Safety, Pharmacokinetics, and Anti-Tumor Activity of CUDC-101 in Patients With Advanced Solid Tumors

Start: Aug 2008Est. completion: Apr 201025 patients
Phase 1Completed

Study of Dasatinib (BMS-354825) in Patients With Solid Tumors

Start: Jan 2007Est. completion: Sep 200816 patients
Phase 1Completed

Dose Escalation Study of SH U04722 in Solid Tumors

Start: Jan 2007Est. completion: Oct 200710 patients
Phase 1Terminated

A Study Of The Safety And Tolerability Of HKI-272 Administered Orally To Japanese Subjects With Advanced Solid Tumors

Start: Nov 2006Est. completion: Mar 200921 patients
Phase 1Completed

LBH589 in Adult Patients With Advanced Solid Tumors or Cutaneous T-cell Lymphoma

Start: Nov 200614 patients
Phase 1Completed

A Phase 1, Open-Label, Randomized, Cross-Over, Pharmacokinetic Study Evaluating the Effect of S-1 on Advanced Solid Tumors

Start: Sep 2006Est. completion: May 200712 patients
Phase 1Completed

Efficacy and Safety of Patupilone in Patients With Advanced Solid Tumors in Japan

Start: Aug 200615 patients
Phase 1Completed
NCT00373490MSDVorinostat

A Study of Oral Suberoylanilide Hydroxamic Acid (Vorinostat) in Patients With Solid Tumors (0683-048)

Start: Jul 2006Est. completion: Oct 200716 patients
Phase 1Completed

A Dose-escalation Study of BIBF 1120 in Japanese Patients With Advanced Solid Tumours

Start: Jun 200624 patients
Phase 1Completed

AZD1152 in Patients With Advanced Solid Malignancies

Start: May 2006Est. completion: Mar 201743 patients
Phase 1Completed

Study Evaluating SKI-606 in Subject With Solid Tumors

Start: Feb 2006Est. completion: Dec 200828 patients
Phase 1Completed

Study of Oral CNF2024 (BIIB021) in Advanced Solid Tumors

Start: Feb 2006Est. completion: Apr 200970 patients
Phase 1Completed

Study Evaluating TTI-237 in Advanced Malignant Solid Tumors.

Start: Aug 200545 patients
Phase 1Terminated
NCT00127127MSDvorinostat

A Study of Vorinostat in Patients With Solid Tumors (MK-0683-029)

Start: Jun 2005Est. completion: Aug 200918 patients
Phase 1Completed

Study Evaluating TTI-237 in Advanced Malignant Solid Tumors

Start: May 200545 patients
Phase 1Terminated

Safety and Tolerability of hCBE-11 in Subjects With Advanced Solid Tumors

Start: Jan 2005Est. completion: Aug 200613 patients
Phase 1Terminated

A Phase I Study of BMS-275183 Given on a Daily Schedule in Patients With Advanced Malignancies

Start: Oct 200460 patients
Phase 1Terminated

Everolimus for Treating Pediatric Patients With Recurrent or Refractory Tumors

Start: Oct 2004Est. completion: Oct 200841 patients
Phase 1Completed

An Dose Escalation Study of Treatment With BIBF 1120 in Patients With Advanced Solid Tumours

Start: Jun 200350 patients
Phase 1Completed
NCT00060645MSDridaforolimus

Safety Study of AP23573 in Patients With Advanced, Refractory or Recurrent Malignancies (8669-013)(COMPLETED)

Start: May 2003Est. completion: Feb 200933 patients
Phase 1Completed
NCT00060632MSDridaforolimus

Safety Study of Ridaforolimus in Patients With Advanced, Refractory or Recurrent Malignancies (MK-8669-001 AM5)(COMPLETED)

Start: Apr 2003Est. completion: Oct 200546 patients
Phase 1Completed

Elitek (Rasburicase) Immuno-Monitoring Study

Start: Feb 2010Est. completion: Feb 20101 patients
N/ATerminated

Rasburicase Treatment for Chemotherapy or Malignancy-Induced Hyperuricemia in Asthma/Allergy Patients

Start: Mar 2005Est. completion: Feb 201016 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

26 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.