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Advanced Malignant Solid Tumor

Oncology
5
Pipeline Programs
8
Companies
9
Clinical Trials
5 recruiting
0
Approved Products

Pipeline by Development Stage

Preclinical
Phase 1
Phase 1/2
Phase 2
Phase 2/3
Phase 3
On Market
0
4
1
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

8 companies ranked by most advanced pipeline stage

Repertoire Immune Medicines
1 program
1
RPTR-1-201Phase 1/21 trial
Active Trials
NCT07293754Recruiting150Est. Apr 2029
Genmab
GenmabNetherlands - Utrecht
1 program
1
BNT314Phase 11 trial
Active Trials
NCT06150183Active Not Recruiting41Est. Mar 2028
BioNTech
BioNTechCA - San Diego
1 program
1
BNT314Phase 1
Biocorp
BiocorpFrance - Issoire
1 program
1
MT027 cells suspensionPhase 11 trial
Active Trials
NCT06726564Recruiting18Est. Feb 2029
Pilatus Biosciences
Pilatus BiosciencesSwitzerland - Epalinges
1 program
1
PLT012Phase 11 trial
Active Trials
NCT07337525Recruiting36Est. Jan 2028
Virogin Biotech
Virogin BiotechBC - Richmond
3 programs
Recombinant Human IL12/15 Dual-Regulated Oncolytic HSV-1 InjectionPHASE_11 trial
Recombinant Human IL12/15 Dual-Regulated Oncolytic HSV-1 InjectionPHASE_11 trial
Recombinant Human IL12/15-PDL1B Oncolytic HSV-1 InjectionPHASE_11 trial
Active Trials
NCT05477849Recruiting30Est. Dec 2025
NCT07262164Recruiting30Est. Aug 2028
NCT04758897Unknown18Est. Dec 2022
Molecular Partners
Molecular PartnersSchlieren-Zurich, Switzerland
1 program
MP0317, a tri-specific fibroblast activation proteinPHASE_11 trial
Active Trials
NCT05098405Terminated46Est. Jan 2024
Chia Tai TianQing Pharmaceutical Group
1 program
TQB3303PHASE_11 trial
Active Trials
NCT04275050Unknown40Est. Apr 2022

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
2028
2029
Repertoire Immune MedicinesRPTR-1-201
Virogin BiotechRecombinant Human IL12/15 Dual-Regulated Oncolytic HSV-1 Injection
Pilatus BiosciencesPLT012
BiocorpMT027 cells suspension
GenmabBNT314
Virogin BiotechRecombinant Human IL12/15 Dual-Regulated Oncolytic HSV-1 Injection
Molecular PartnersMP0317, a tri-specific fibroblast activation protein
Virogin BiotechRecombinant Human IL12/15-PDL1B Oncolytic HSV-1 Injection
Chia Tai TianQing Pharmaceutical GroupTQB3303

Clinical Trials (9)

Total enrollment: 409 patients across 9 trials

An Early Phase Trial of RPTR-1-201 in Advanced Solid Tumors

Start: Dec 2025Est. completion: Apr 2029150 patients
Phase 1/2Recruiting
NCT07262164Virogin BiotechRecombinant Human IL12/15 Dual-Regulated Oncolytic HSV-1 Injection

A Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Biologic Effect of VG2062 in Patients With Solid Tumors

Start: Mar 2026Est. completion: Aug 202830 patients
Phase 1Recruiting

A First in Human Study of PLT012 in Participants With Solid Tumor Cancers

Start: Feb 2026Est. completion: Jan 202836 patients
Phase 1Recruiting
NCT06726564BiocorpMT027 cells suspension

A Study of MT027 in Patients with Pleural Malignant Tumors

Start: May 2024Est. completion: Feb 202918 patients
Phase 1Recruiting

Safety and Preliminary Efficacy of BNT314 in Cancer Patients With Malignant Solid Tumors

Start: Nov 2023Est. completion: Mar 202841 patients
Phase 1Active Not Recruiting
NCT05477849Virogin BiotechRecombinant Human IL12/15 Dual-Regulated Oncolytic HSV-1 Injection

A Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Biologic Effect of VG2025 in Patients with Solid Tumors

Start: Aug 2022Est. completion: Dec 202530 patients
Phase 1Recruiting
NCT05098405Molecular PartnersMP0317, a tri-specific fibroblast activation protein

First-in-human Safety and Tolerability of MP0317 in Patients With Relapsed/Refractory Advanced Solid Tumors

Start: Oct 2021Est. completion: Jan 202446 patients
Phase 1Terminated
NCT04758897Virogin BiotechRecombinant Human IL12/15-PDL1B Oncolytic HSV-1 Injection

Clinical Study of VG161 in Subjects With Advanced Malignant Solid Tumors

Start: Apr 2021Est. completion: Dec 202218 patients
Phase 1Unknown

A Study to Evaluate the Tolerance and Pharmacokinetics of TQB3303 Tablets

Start: Apr 2020Est. completion: Apr 202240 patients
Phase 1Unknown

Related Jobs in Oncology

Phase Legend

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

Key Insights

5 actively recruiting trials targeting 409 patients
8 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.