Senior Biostatistician - Oncology (FSP -Permanent Homebased)
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 .
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