Global Cancer Research Analyst
5 days ago
This is a permanent, home-based opportunity to work on late-phase global oncology trials with a focus on hematology and regulatory submissions.
As the lead statistician on these trials, you will serve as the key statistical contributor in 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.
- Contribute to study design and development of statistical analysis plans (SAPs).
- Collaborate with cross-functional teams to ensure timely delivery of statistical deliverables.
- Develop and implement statistical programming for data analysis and reporting.
- Provide statistical guidance and support for regulatory submissions.
- 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.
- Work from home permanently with a flexible schedule.
- Opportunity to work on high-impact global studies with a focus on improving cancer treatment outcomes.
- Be part of a collaborative and innovative team environment.
IQVIA is a leading provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences industry. We create intelligent connections to accelerate medical innovation and improve patient outcomes worldwide.
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