Senior Biostatistician – Oncology (FSP -Permanent Homebased)

Reposted 3 Hours Ago
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14 Locations
In-Office
Senior level
Healthtech
The Role
The Senior Biostatistician will lead statistical efforts on global late-phase oncology trials, focusing on study design, analysis plans, and regulatory submissions while ensuring compliance and accuracy in deliverables.
Summary Generated by Built In

We are seeking an experienced and proactive Senior Biostatistician to join our FSP team, supporting a global pharmaceutical client. This is a permanent, home-based position offering the opportunity to work on late-phase global oncology trials, with a focus on hematology and regulatory submissions.

Key Responsibilities
  • Serve as the lead statistician on global late-phase registration trials, particularly in oncology (hematology preferred).
  • Independently contribute to study design, statistical analysis plans (SAPs), and regulatory submission strategies.
  • Participate in study team meetings, providing statistical guidance and collaborating with cross-functional teams.
  • Address health authority questions and support responses with appropriate statistical analyses and documentation.
  • Perform hands-on statistical programming to derive outputs and summary statistics using ADaM and SDTM datasets.
  • Ensure timely and accurate delivery of statistical deliverables in compliance with regulatory standards
Required Qualifications
  • Advanced degree (Master’s or PhD) in Biostatistics, Statistics, or a related field.
  • 5+ years of experience in clinical trials, with a strong focus on oncology (hematology and late-phase preferred).
  • Proven experience working on registrational studies and regulatory submissions.
  • Strong knowledge of CDISC standards, particularly ADaM and SDTM.
  • Proficiency in SAS programming and ability to perform hands-on statistical analyses.
  • Excellent communication skills and ability to work independently in a global, cross-functional environment.
Preferred Experience
  • Prior involvement in FDA/EMA submissions.
  • Experience addressing regulatory agency queries.
  • Familiarity with real-world evidence and observational studies is a plus.
Why Join Us?
  • Work on high-impact global studies with a focus on improving cancer treatment outcomes.
  • Be part of a collaborative and innovative team environment.
  • Enjoy the flexibility of remote work with a permanent contract.
  • Gain exposure to regulatory strategy and cutting-edge oncology research.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

Top Skills

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The Company
Bangalore, Karnataka
61,500 Employees
Year Founded: 2016

What We Do

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 70,000 employees, IQVIA conducts operations in more than 100 countries. To learn more, visit www.iqvia.com.

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