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Liver Metastases

Oncology
5
Pipeline Programs
9
Companies
8
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
4
0
1
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Cell Therapy
375%
Monoclonal Antibody
125%
+ 4 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

8 companies ranked by most advanced pipeline stage

Amgen
AmgenTHOUSAND OAKS, CA
1 program
1
AdecatumumabPhase 2Monoclonal Antibody1 trial
Active Trials
NCT00866944Completed35Est. Nov 2011
Navidea Biopharmaceuticals
1 program
1
TilmanoceptPhase 11 trial
Active Trials
NCT03029988Terminated3Est. Sep 2018
Colorado Therapeutics
Colorado TherapeuticsCO - Louisville
1 program
1
anti-CEA CAR-T cellsPhase 1Cell Therapy
Sirtex Medical
Sirtex MedicalGermany - Bonn
1 program
1
anti-CEA CAR-T cellsPhase 1Cell Therapy1 trial
Active Trials
NCT02416466Completed8Est. Jun 2018
Sorrento Therapeutics
Sorrento TherapeuticsCA - San Diego
1 program
1
anti-CEA CAR-T cellsPhase 1Cell Therapy1 trial
Active Trials
NCT02850536Completed5Est. Sep 2021
Alpha Tau Medical
Alpha Tau MedicalJERUSALEM, Israel
1 program
Diffusing Alpha Radiation Emitters TherapyN/A2 trials
Active Trials
NCT05829291Recruiting10Est. Feb 2026
NCT05047094Recruiting48Est. Jun 2027
Medica Corp
Medica CorpMA - Bedford
1 program
Use of DwI-MR to Predict Chemotherapy Response of Liver Metastases and HepatocarcinomaN/A1 trial
Active Trials
NCT01411579Completed57Est. Feb 2013
City Therapeutics
City TherapeuticsMA - Cambridge
1 program
gemcitabine hydrochloridePHASE_1_21 trial
Active Trials
NCT00645710CompletedEst. Feb 2018

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
2027
AmgenAdecatumumab
City Therapeuticsgemcitabine hydrochloride
Navidea BiopharmaceuticalsTilmanocept
Sorrento Therapeuticsanti-CEA CAR-T cells
Sirtex Medicalanti-CEA CAR-T cells
Alpha Tau MedicalDiffusing Alpha Radiation Emitters Therapy
Alpha Tau MedicalDiffusing Alpha Radiation Emitters Therapy
Medica CorpUse of DwI-MR to Predict Chemotherapy Response of Liver Metastases and Hepatocarcinoma

Clinical Trials (8)

Total enrollment: 166 patients across 8 trials

NCT00866944AmgenAdecatumumab

Study of Adecatumumab Relative to FOLFOX After R0 Resection of Colorectal Liver Metastases

Start: Mar 2009Est. completion: Nov 201135 patients
Phase 2Completed
NCT00645710City Therapeuticsgemcitabine hydrochloride

Hepatic Arterial Infusion of Floxuridine, Gemcitabine Hydrochloride, and Radiolabeled Monoclonal Antibody Therapy in Treating Liver Metastases in Patients With Metastatic Colorectal Cancer Previously Treated With Surgery

Start: Feb 2005Est. completion: Feb 2018
Phase 1/2Completed

An Evaluation of Tilmanocept by IV Injection Using SPECT/CT vs PET Imaging in Subjects With Liver Metastases.

Start: Jul 2017Est. completion: Sep 20183 patients
Phase 1Terminated

CAR-T Hepatic Artery Infusions or Pancreatic Venous Infusions for CEA-Expressing Liver Metastases or Pancreas Cancer

Start: Feb 2017Est. completion: Sep 20215 patients
Phase 1Completed
NCT02416466Sirtex Medicalanti-CEA CAR-T cells

CAR-T Hepatic Artery Infusions and Sir-Spheres for Liver Metastases

Start: Apr 2015Est. completion: Jun 20188 patients
Phase 1Completed
NCT05829291Alpha Tau MedicalDiffusing Alpha Radiation Emitters Therapy

Alpha Radiation Emitters Device for the Treatment of Liver Metastases (DaRT)

Start: Oct 2023Est. completion: Feb 202610 patients
N/ARecruiting
NCT05047094Alpha Tau MedicalDiffusing Alpha Radiation Emitters Therapy

Alpha Radiation Emitters Device (DaRT) in Combination With Check Point Inhibitor for the Treatment of Recurrent Unresectable or mHNSCC

Start: Nov 2021Est. completion: Jun 202748 patients
N/ARecruiting
NCT01411579Medica CorpUse of DwI-MR to Predict Chemotherapy Response of Liver Metastases and Hepatocarcinoma

Use of DwI-MR to Predict Chemotherapy Response of Liver Metastases and Hepatocarcinoma

Start: Feb 2011Est. completion: Feb 201357 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 166 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.