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Solid Tumor Cancer

Oncology
8
Pipeline Programs
9
Companies
10
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
6
2
0
0
0
0
Early DiscoveryClinical DevelopmentMarket

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

9 companies ranked by most advanced pipeline stage

GV20 Therapeutics
GV20 TherapeuticsChina - Shanghai
1 program
1
GV20-0251Phase 1/21 trial
Active Trials
NCT07070518Recruiting350Est. Sep 2028
Ranok Therapeutics
Ranok TherapeuticsChina - Hangzhou
1 program
1
IN10018 in combination with RNK08954Phase 1/2
ViiV Healthcare
ViiV HealthcareNC - Durham
5 programs
5
IspinesibPhase 1
SB-485232Phase 1
SB-485232Phase 1
SB-743921Phase 1
docetaxelPhase 1
Genor Biopharma
Genor BiopharmaChina - Shanghai
1 program
1
GB268Phase 11 trial
Active Trials
NCT06934616Not Yet Recruiting330Est. Mar 2028
GSK
GSKLONDON, United Kingdom
5 programs
IspinesibPHASE_11 trial
SB-485232PHASE_11 trial
SB-485232PHASE_11 trial
SB-743921PHASE_11 trial
docetaxelPHASE_11 trial
Active Trials
NCT00119171Completed30
NCT00085904Completed12
NCT00085878Completed25
+2 more trials
BioTherapeutics Inc
BioTherapeutics IncVA - Blacksburg
1 program
No additional intervention administered in this long term follow-up studyN/A1 trial
Active Trials
NCT06885424Enrolling By Invitation400Est. Mar 2040
A2 Biotherapeutics
A2 BiotherapeuticsCA - Agoura Hills
1 program
No additional intervention administered in this long term follow-up studyN/A
Qilu Pharmaceutical
Qilu PharmaceuticalChina - Jinan
1 program
QLS5212PHASE_11 trial
Active Trials
NCT07467629Not Yet Recruiting100Est. Apr 2028
InxMed
InxMedChina - Beijing
1 program
IN10018 in combination with RNK08954PHASE_1_21 trial
Active Trials
NCT07441174Recruiting92Est. Feb 2031

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
2030
2031
InxMedIN10018 in combination with RNK08954
GV20 TherapeuticsGV20-0251
Qilu PharmaceuticalQLS5212
Genor BiopharmaGB268
GSKIspinesib
GSKdocetaxel
GSKSB-743921
GSKSB-485232
GSKSB-485232
BioTherapeutics IncNo additional intervention administered in this long term follow-up study

Clinical Trials (10)

Total enrollment: 1,399 patients across 10 trials

NCT07441174InxMedIN10018 in combination with RNK08954

IN10018 in Combination With RNK08954 for the Treatment of KRASG12D Mutation-Positive Locally Advanced or Metastatic Solid Tumors

Start: Feb 2026Est. completion: Feb 203192 patients
Phase 1/2Recruiting

Study of GV20-0251 in Participants With Solid Tumor Malignancies

Start: Jul 2025Est. completion: Sep 2028350 patients
Phase 1/2Recruiting

QLS5212 for Participants With Advanced Solid Tumors

Start: Apr 2026Est. completion: Apr 2028100 patients
Phase 1Not Yet Recruiting

A Phase I, First-in-Human Study of GB268 (PD-1/CTLA-4/VEGF Trispecific Antibody) in Advanced Solid Tumors

Start: Apr 2025Est. completion: Mar 2028330 patients
Phase 1Not Yet Recruiting

Ispinesib In Combination With Capecitabine In Patients With Solid Tumors

Start: Nov 200430 patients
Phase 1Completed

SB-715992 In Combination With Docetaxel In Patients With Solid Tumors

Start: Jun 200430 patients
Phase 1Completed

SB-743921 In Patients With Solid Tumors

Start: Apr 200430 patients
Phase 1Completed

Dose-Escalating Study Of SB-485232 Administered Intravenously Every 28 Days To Adults With Solid Tumors Or Lymphomas

Start: Apr 200412 patients
Phase 1Completed

Dose-Escalation Study Of SB-485232 Administered As Daily Subcutaneous Injections In Adults With Solid Tumors

Start: Jan 200325 patients
Phase 1Completed
NCT06885424BioTherapeutics IncNo additional intervention administered in this long term follow-up study

A Long-Term Follow-Up Study of Participants Treated With A2 Biotherapeutics (A2 Bio) Gene Therapy (GT) Products

Start: Aug 2025Est. completion: Mar 2040400 patients
N/AEnrolling By Invitation

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 1,399 patients
9 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.