Your oncology discovery deserves an innovative approach

 

Specialized solutions to accelerate your breakthrough

Every year across the globe, cancer affects the quality of life for millions of people. The far-reaching impact of cancer and demand for treatments that improve duration and outcomes for patients inspires a race for biotech companies to develop new therapeutics.

However, with complex oncology trials and the many unknowns that come with next generation therapies, there are endless hurdles. Your scientific discoveries deserve an innovative approach to clinical development.

Streamlined clinical development approaches, coupled with effective CRO-sponsor partnerships, not only result in success for emerging biopharma companies, but can also generate tremendous value for patients. As a full-service oncology CRO, we are dedicated to supporting biotech and emerging biopharma companies through every phase of development. Our extensive oncology expertise coupled with an end-to-end approach helps accelerate your clinical programs, giving you confidence to bring breakthrough treatments to patients.

Oncology clinical trial expertise

Our strong foundation of therapeutic, scientific, and operational expertise enables us to bring unparalleled innovation to oncology clinical development, making your trial more precise, predictable and efficient.

  • 500+ studies in the past 5 years 
  • Experience working in more than 50 countries 
  • 16 FDA approved oncology therapies
  • Board-certified oncologists and hematologists on staff
  • Global oncology key opinion leaders and site networks
  • Global oncology regulatory expertise 
EARLY PHASE ONCOLOGY

Our extensive early phase oncology experience enables us to guide your program through the intricacies inherent in dose-finding and dose-optimization, safety and proof-of-concept studies in a sick patient population. We look beyond first-in-human, and are active in a range of adaptive, basket and umbrella designs, as well as complex multi-arm platform design trials.

  • Global network of specialist Phase I oncology sites
  • Technology solutions for enhanced cohort planning and management
  • Modeling and simulation of multiple datasets to identify optimal dose of novel targeted and immune therapies
  • Laboratory services from Q2 Solutions for biomarker services, assay validation and development of companion diagnostics
LATE PHASE ONCOLOGY

We offer modern solutions for patient-focused trials that accelerate enrollment, reduce site burden, and deliver trials on time and budget.

  • Proven decentralized trial solutions
  • Global network of trial sites to optimize patient recruitment
  • Precision site selection, centralized monitoring, and automated safety case processing
  • Global regulatory expertise
Experience by phase

Early and late phase expertise

IQVIA Biotech has staff with specific early phase and late phase experience to address the nuances of different phases of development and can grow with you as your pipeline matures.

ONCOLOGY INSIGHTS

Our experienced oncology teams are here to support your clinical trial in any indication

  • Bladder
  • Breast
  • Cervical
  • Colorectal
  • Dermatologic oncology
  • Gastroesophageal junction
  • Glioblastoma multiforme
  • Gynecological
  • Head and neck
 
  • Hematologic malignancies
  • Kidney 
  • Leukemia
  • Liver 
  • Lymphoma
  • Lung 
  • Melanoma
  • Mesothelioma
  • Multiple myeloma
 
  • Myelodysplastic syndrome
  • Neuro 
  • Ovarian
  • Pancreatic
  • Prostate 
  • Renal 
  • Soft tissue sarcoma 
  • Solid tumor
  • Supportive care
 

Connected Intelligence for oncology clinical development

Our powerful approach brings together oncology experts, data-driven insights, global site networks, and innovative technologies to help you drive smarter decisions to accelerate clinical development.

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IQVIA Biotech's Oncology Resource Center

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