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Metastatic

Oncology
0
Pipeline Programs
1
Companies
24
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
0
0
0
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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

1 companies ranked by most advanced pipeline stage

Sanofi
SanofiPARIS, France
1 program
ZD6474PHASE_15 trials
Active Trials
NCT00752986Terminated39Est. Sep 2013
NCT00753714Completed124Est. Dec 2011
NCT00659438Completed95Est. Jul 2011
+2 more trials

Trial Timeline

Clinical trial activity over time

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2026
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Showing 15 of 24 trials with date data

Clinical Trials (24)

Total enrollment: 4,313 patients across 24 trials

An Efficacy Study Comparing ZD6474 to Placebo in Medullary Thyroid Cancer

Start: Nov 2006Est. completion: Jul 2024331 patients
Phase 3Completed

ZD6474 (ZACTIMA™) Phase III Study in EGFR Failures

Start: Nov 2006Est. completion: Nov 20141,140 patients
Phase 3Completed

Efficacy Trial Comparing ZD6474 With Erlotinib in NSCLC After Failure of at Least One Prior Chemotherapy

Start: Aug 2006Est. completion: Nov 20161,574 patients
Phase 3Completed

ZACtima FASlodex Trial in Postmenopausal Advance Breast Cancer Patients Instead of ZACtima FASlodex Trial

Start: Dec 2008Est. completion: Sep 201339 patients
Phase 2Terminated

Zactima in Non Small Cell Lung Cancer (NSCLC) ELderly Patients In Combination With or Versus Gemcitabine

Start: Oct 2008Est. completion: Dec 2011124 patients
Phase 2Completed

Efficacy and Safety of Zactima™ in Patients With Castration-refractory Metastatic Prostate Cancer

Start: Feb 2008Est. completion: Jul 201195 patients
Phase 2Completed

Efficacy and Safety of Vandetanib (ZD6474) in Patients With Metastatic Papillary or Follicular Thyroid Cancer

Start: Sep 2007Est. completion: Nov 2021164 patients
Phase 2Completed

Phase II Study of Best Support Care (BSC) Plus ZD6474(Vandetanib) in Patients With Inoperable Hepatocellular Carcinoma (HCC)

Start: Jul 2007Est. completion: Jun 200967 patients
Phase 2Completed

A Phase II, Double Blind Study of 2 Doses of ZACTIMA™(ZD6474) in Combination With FOLFIRI vs FOLFIRI Alone for the Treatment of Colorectal Cancer in Patients

Start: Mar 2007Est. completion: Nov 2009106 patients
Phase 2Completed

A Study To Assess ZD6474 (ZACTIMA™) Monotherapy In Locally Advanced or Metastatic Hereditary Medullary Thyroid Cancer

Start: Aug 2006Est. completion: May 201419 patients
Phase 2Completed

E3 Breast Cancer Taxotere Combination

Start: Jan 2006Est. completion: Jan 200964 patients
Phase 2Completed

ZD6474 Phase IIa Dose Finding Multicentre Study

Start: Dec 2004Est. completion: Jan 200753 patients
Phase 2Completed

Efficacy and Tolerability of ZD6474 in Patients With Thyroid Cancer

Start: Nov 2004Est. completion: Apr 201740 patients
Phase 2Completed

ZD6474 Alone or in Combination With Paclitaxel and Carboplatin in Subjects With Previously Untreated Locally Advanced or Metastatic Non-small Cell Lung Cancer (NSCLC)

Start: Feb 2004Est. completion: Oct 2007
Phase 2Completed

This Study is to Compare the Efficacy of ZD6474 and ZD1839 in Subjects With NSCLC.

Start: May 2003Est. completion: Jun 2007160 patients
Phase 2Completed

ZD6474 in Treating Patients With Small Cell Lung Cancer

Start: May 2003Est. completion: Dec 2006
Phase 2Completed

Efficacy Study of ZD6474 to Treat Multiple Myeloma Cancer

Start: Oct 2002Est. completion: May 200430 patients
Phase 2Completed

This Study is to Assess the Efficacy and Safety of ZD6474 in Subjects With Non-small Cell Lung Cancer.

Start: Oct 2002Est. completion: Sep 2006129 patients
Phase 2Completed

This Study is to Assess the Efficacy and Safety of ZD6474 in Subjects With Metastatic Breast Cancer

Start: May 2002Est. completion: Nov 200344 patients
Phase 2Completed

Open Label, Phase I ZD6474 Head and Neck Cancer Study

Start: Dec 2006Est. completion: Nov 201148 patients
Phase 1Completed

Phase I Efficacy On Vascular Permeability In Patients With Advanced Colorectal Cancer

Start: Aug 2006Est. completion: Oct 200724 patients
Phase 1Completed

Phase I Combination With Vinorelbine or Gemcitabine Plus Cisplatin in Locally Advanced or Metastatic NSCLC

Start: Aug 2006Est. completion: May 200717 patients
Phase 1Completed

Phase I Irinotecan, 5-Fluorouracil and Leucovorin Combination

Start: Aug 2005Est. completion: Jun 200824 patients
Phase 1Completed

ZD6474(Vandetanib) + Alimta Combo Study

Start: Jul 2005Est. completion: Oct 201121 patients
Phase 1Completed

Related Jobs in Oncology

Phase Legend

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

Key Insights

1 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.