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Non-Hodgkins Lymphoma

Oncology
6
Pipeline Programs
9
Companies
10
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
4
1
1
0
0
0
Early DiscoveryClinical DevelopmentMarket

Drug Modality Breakdown

Monoclonal Antibody
583%
ADC
117%
+ 6 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

9 companies ranked by most advanced pipeline stage

Bayer
BayerLEVERKUSEN, Germany
2 programs
1
1
RituximabPhase 2Monoclonal Antibody1 trial
RituximabPhase 1/2Monoclonal Antibody1 trial
Active Trials
NCT00807196Unknown20Est. Dec 2012
NCT00193466Completed40Est. Apr 2008
Hope Medicine
Hope MedicineChina - Pudong
1 program
1
EBV CTL'sPhase 11 trial
Active Trials
NCT02057445Completed1Est. Dec 2017
Utah Medical
Utah MedicalIreland - Dublin
1 program
1
EBV CTL'sPhase 1
Sandoz
SandozAustria - Kundl
1 program
1
JBH492Phase 11 trial
Active Trials
NCT04240704Terminated25Est. Sep 2024
Kite Pharma
Kite PharmaCA - El Segundo
1 program
1
hLL2Phase 11 trial
Active Trials
NCT00054834Terminated27
TG Therapeutics
TG TherapeuticsNEW YORK, NY
2 programs
UblituximabPHASE_1Monoclonal Antibody1 trial
UblituximabPHASE_1_2Monoclonal Antibody1 trial
Active Trials
NCT01744912Terminated10Est. Feb 2014
NCT01647971Completed39Est. May 2015
Biogen
BiogenCAMBRIDGE, MA
2 programs
IfosfamidePHASE_21 trial
RituximabPHASE_2Monoclonal Antibody1 trial
Active Trials
NCT00193505Completed40Est. Aug 2005
NCT00193440Completed40Est. Jan 2009
Novartis
NovartisBASEL, Switzerland
1 program
JBH492PHASE_1
Genentech
GenentechCA - Oceanside
1 program
Polatuzumab VedotinPHASE_1ADC1 trial
Active Trials
NCT01290549Completed95Est. Nov 2014

Trial Timeline

Clinical trial activity over time

2021
2022
2023
2024
2025
2026
BiogenIfosfamide
BiogenRituximab
BayerRituximab
TG TherapeuticsUblituximab
BayerRituximab
SandozJBH492
Hope MedicineEBV CTL's
TG TherapeuticsUblituximab
GenentechPolatuzumab Vedotin
Kite PharmahLL2

Clinical Trials (10)

Total enrollment: 337 patients across 10 trials

Ifosfamide/Carboplatin/Etoposide/Rituxan Followed by Zevalin in Relapsed/Refractory Intermediate Grade B-Cell Lymphoma

Start: Oct 2003Est. completion: Aug 200540 patients
Phase 2Completed

Rituximab and Chemotherapy Followed by Ibritumomab Tiuxetan as Treatment for Low Grade Follicular Non-Hodgkin's Lymphoma

Start: Apr 2002Est. completion: Jan 200940 patients
Phase 2Completed

Rituximab and Fludarabine Followed by CAMPATH-1H in Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma

Start: Jan 2002Est. completion: Apr 200840 patients
Phase 2Completed

Study of the Efficacy and Safety of Ublituximab in Patients With Relapsed or Refractory B-cell Non-Hodgkin Lymphoma

Start: Jul 2012Est. completion: May 201539 patients
Phase 1/2Completed

Zevalin With Non Myeloablative Allogeneic Stem Cell Transplantation in Patients With Non Hodgkin Lymphoma

Start: Sep 2008Est. completion: Dec 201220 patients
Phase 1/2Unknown

Safety and Preliminary Efficacy of JBH492 Monotherapy in Patients With CLL and NHL

Start: Sep 2020Est. completion: Sep 202425 patients
Phase 1Terminated

3rd Party LMP1/2-Specific Cytotoxic T Lymphocytes for EBV-Associated Lymphoma

Start: Jan 2014Est. completion: Dec 20171 patients
Phase 1Completed

Ublituximab in Combination With Lenalidomide in Patients With B-Cell Lymphoid Malignancies

Start: Nov 2012Est. completion: Feb 201410 patients
Phase 1Terminated
NCT01290549GenentechPolatuzumab Vedotin

A Study of Escalating Doses of Polatuzumab Vedotin in Participants With Relapsed or Refractory B-Cell Non-Hodgkins Lymphoma and Chronic Lymphocytic Leukemia and Polatuzumab Vedotin in Combination With Rituximab in Participants With Relapsed or Refractory B-Cell Non-Hodgkins Lymphoma

Start: Mar 2011Est. completion: Nov 201495 patients
Phase 1Completed

Study of 90Y-hLL2 to Treat Non-Hodgkin's Lymphoma

Start: Mar 200327 patients
Phase 1Terminated

Related Jobs in Oncology

Phase Legend

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

Key Insights

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.